Year |
Citation |
Score |
2008 |
Ruigrok YM, Wijmenga C, Rinkel GJ, van't Slot R, Baas F, Wolfs M, Westerveld A, Roos YB. Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32. Stroke; a Journal of Cerebral Circulation. 39: 1096-102. PMID 18309175 DOI: 10.1161/Strokeaha.107.495168 |
0.336 |
|
2001 |
Luijten M, Redeker S, Minoshima S, Shimizu N, Westerveld A, Hulsebos TJ. Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22. Human Genetics. 109: 109-16. PMID 11479742 DOI: 10.1007/S004390100543 |
0.35 |
|
2001 |
Luijten M, Fahsold R, Mischung C, Westerveld A, Nürnberg P, Hulsebos TJ. Limited contribution of interchromosomal gene conversion to NF1 gene mutation. Journal of Medical Genetics. 38: 481-5. PMID 11476066 DOI: 10.1136/Jmg.38.7.481 |
0.346 |
|
2000 |
Steenman MJ, Zijlstra N, Kruitbosch DL, Wiesmeijer C, Larizza L, Voûte PA, Westerveld A, Mannens MM. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors. Cytogenetics and Cell Genetics. 88: 289-95. PMID 10828613 DOI: 10.1159/000015542 |
0.385 |
|
2000 |
Luijten M, Wang Y, Smith BT, Westerveld A, Smink LJ, Dunham I, Roe BA, Hulsebos TJ. Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22. European Journal of Human Genetics : Ejhg. 8: 209-14. PMID 10780787 DOI: 10.1038/Sj.Ejhg.5200434 |
0.382 |
|
2000 |
Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome. American Journal of Human Genetics. 66: 1473-84. PMID 10762538 DOI: 10.1086/302892 |
0.369 |
|
1999 |
van der Drift P, Chan A, Zehetner G, Westerveld A, Versteeg R. Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expanding genomic graveyard? Genomics. 62: 74-81. PMID 10585770 DOI: 10.1006/Geno.1999.5972 |
0.313 |
|
1999 |
Hulsebos TJ, Oskam NT, Bijleveld EH, Westerveld A, Hermsen MA, van den Ouweland AM, Hamel BC, Tijssen CC. Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2. British Journal of Cancer. 81: 1150-4. PMID 10584875 DOI: 10.1038/Sj.Bjc.6690822 |
0.409 |
|
1999 |
Steenman M, Tomlinson G, Westerveld A, Mannens M. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma. Cytogenetics and Cell Genetics. 86: 157-61. PMID 10545709 DOI: 10.1159/000015371 |
0.36 |
|
1999 |
den Hollander AI, ten Brink JB, de Kok YJ, van Soest S, van den Born LI, van Driel MA, van de Pol DJ, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, et al. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genetics. 23: 217-21. PMID 10508521 DOI: 10.1038/13848 |
0.354 |
|
1999 |
van Soest S, van Rossem MJ, Heckenlively JR, van den Born LI, de Meulemeester TM, Vliex S, de Jong PT, Bleeker-Wagemakers EM, Westerveld A, Bergen AA. Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes. Cytogenetics and Cell Genetics. 84: 22-7. PMID 10343093 DOI: 10.1159/000015204 |
0.393 |
|
1997 |
Hermsen MA, Joenje H, Arwert F, Braakhuis BJ, Baak JP, Westerveld A, Slater R. Assessment of chromosomal gains and losses in oral squamous cell carcinoma by comparative genomic hybridisation. Oral Oncology. 33: 414-8. PMID 9509125 DOI: 10.1016/S0964-1955(97)00031-6 |
0.388 |
|
1997 |
Voesten AM, Bijleveld EH, Westerveld A, Hulsebos TJ. Fine mapping of a region of common deletion on chromosome arm 10p in human glioma. Genes, Chromosomes & Cancer. 20: 167-72. PMID 9331567 DOI: 10.1002/(Sici)1098-2264(199710)20:2<167::Aid-Gcc7>3.0.Co;2-1 |
0.398 |
|
1997 |
Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voûte PA, Westerveld A, Slater R, Mannens M. Comparative genomic hybridization analysis of Wilms tumors. Cytogenetics and Cell Genetics. 77: 296-303. PMID 9284942 DOI: 10.1159/000134602 |
0.309 |
|
1997 |
Alders M, Hodges M, Hadjantonakis AK, Postmus J, van Wijk I, Bliek J, de Meulemeester M, Westerveld A, Guillemot F, Oudejans C, Little P, Mannens M. The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. Human Molecular Genetics. 6: 859-67. PMID 9175731 DOI: 10.1093/Hmg/6.6.859 |
0.415 |
|
1997 |
Hulsebos TJ, Bijleveld EH, Oskam NT, Westerveld A, Leenstra S, Hogendoorn PC, Bras J. Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas. Genes, Chromosomes & Cancer. 18: 279-85. PMID 9087567 DOI: 10.1002/(Sici)1098-2264(199704)18:4<279::Aid-Gcc5>3.0.Co;2-Y |
0.326 |
|
1996 |
Cheng NC, Chan AJ, Beitsma MM, Speleman F, Westerveld A, Versteeg R. A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1. Human Molecular Genetics. 5: 309-17. PMID 8852654 DOI: 10.1093/Hmg/5.3.309 |
0.335 |
|
1996 |
Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, ... Westerveld A, et al. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Medical and Pediatric Oncology. 27: 490-4. PMID 8827079 DOI: 10.1002/(Sici)1096-911X(199611)27:5<490::Aid-Mpo17>3.0.Co;2-E |
0.399 |
|
1996 |
Hermsen MA, Joenje H, Arwert F, Welters MJ, Braakhuis BJ, Bagnay M, Westerveld A, Slater R. Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma. Genes, Chromosomes & Cancer. 15: 1-9. PMID 8824719 DOI: 10.1002/(Sici)1098-2264(199601)15:1<1::Aid-Gcc1>3.0.Co;2-8 |
0.368 |
|
1996 |
Sijbers AM, van der Spek PJ, Odijk H, van den Berg J, van Duin M, Westerveld A, Jaspers NG, Bootsma D, Hoeijmakers JH. Mutational analysis of the human nucleotide excision repair gene ERCC1. Nucleic Acids Research. 24: 3370-80. PMID 8811092 DOI: 10.1093/Nar/24.17.3370 |
0.543 |
|
1996 |
Hofstra RM, Cheng NC, Hansen C, Stulp RP, Stelwagen T, Clausen N, Tommerup N, Caron H, Westerveld A, Versteeg R, Buys CH. No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma. Human Genetics. 97: 362-4. PMID 8786083 DOI: 10.1007/Bf02185773 |
0.513 |
|
1996 |
van Soest S, te Nijenhuis S, van den Born LI, Bleeker-Wagemakers EM, Sharp E, Sandkuijl LA, Westerveld A, Bergen AA. Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC). Cytogenetics and Cell Genetics. 73: 81-5. PMID 8646891 DOI: 10.1159/000134313 |
0.386 |
|
1996 |
Caron H, van Sluis P, Buschman R, Pereira do Tanque R, Maes P, Beks L, de Kraker J, Voûte PA, Vergnaud G, Westerveld A, Slater R, Versteeg R. Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus. Human Genetics. 97: 834-7. PMID 8641706 DOI: 10.1007/Bf02346199 |
0.575 |
|
1996 |
Caron H, van Sluis P, de Kraker J, Bökkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voûte PA, Versteeg R. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. The New England Journal of Medicine. 334: 225-30. PMID 8531999 DOI: 10.1056/Nejm199601253340404 |
0.564 |
|
1996 |
Voesten A, Bijleveld E, Westerveld A, Hulsebos T. Determination of the smallest region of amplification in chromosomal band 17P12 in malignant astrocytomas Cancer Genetics and Cytogenetics. 91: 172. DOI: 10.1016/S0165-4608(97)82648-9 |
0.342 |
|
1995 |
Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, ... ... Westerveld A, et al. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proceedings of the National Academy of Sciences of the United States of America. 92: 12456-60. PMID 8618920 DOI: 10.1073/Pnas.92.26.12456 |
0.352 |
|
1995 |
Hulsebos TJ, Gilbert DJ, Delattre O, Smink LJ, Dunham I, Westerveld A, Thomas G, Jenkins NA, Copeland NG. Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5. Genomics. 29: 712-8. PMID 8575764 DOI: 10.1006/Geno.1995.9947 |
0.371 |
|
1995 |
van der Drift P, Chan A, Laureys G, van Roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R. Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36. Genes, Chromosomes & Cancer. 14: 35-42. PMID 8527382 DOI: 10.1002/Gcc.2870140107 |
0.382 |
|
1995 |
Redeker E, Alders M, Hoovers JM, Richard CW, Westerveld A, Mannens M. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenetics and Cell Genetics. 68: 222-5. PMID 7842740 DOI: 10.1159/000133917 |
0.361 |
|
1995 |
Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, Laureys G, Michon J, Brugières L, Voûte PA, Westerveld A. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Human Molecular Genetics. 4: 535-9. PMID 7633401 DOI: 10.1093/Hmg/4.4.535 |
0.566 |
|
1995 |
Pronk JC, Gibson RA, Savola A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, Havenga C, Cohn RJ, De Ravel TJ, Roberts I, Westerveld A, et al. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3 Nature Genetics. 11: 338-340. PMID 7581462 DOI: 10.1038/Ng1195-338 |
0.438 |
|
1995 |
Versteeg R, Caron H, Cheng NC, van der Drift P, Slater R, Westerveld A, Voûte PA, Delattre O, Laureys G, Van Roy N. 1p36: every subband a suppressor? European Journal of Cancer (Oxford, England : 1990). 31: 538-41. PMID 7576962 DOI: 10.1016/0959-8049(95)00037-J |
0.475 |
|
1995 |
Bijlsma EK, Voesten AM, Bijleveld EH, Troost D, Westerveld A, Mérel P, Thomas G, Hulsebos TJ. Molecular analysis of genetic changes in ependymomas. Genes, Chromosomes & Cancer. 13: 272-7. PMID 7547635 DOI: 10.1002/Gcc.2870130407 |
0.385 |
|
1995 |
van Soest S, Te Nijenhuis S, van den Born L, Bleeker-Wagemakers E, Sankuul L, Westerveld A, Bergen A. 3233 Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome IQ; exclusion of the phosducin gene Vision Research. 35: S131. DOI: 10.1016/0042-6989(95)90291-0 |
0.37 |
|
1994 |
van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA. Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. Genomics. 22: 499-504. PMID 8001962 DOI: 10.1006/Geno.1994.1422 |
0.314 |
|
1994 |
Leenstra S, Bijlsma EK, Troost D, Oosting J, Westerveld A, Bosch DA, Hulsebos TJ. Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis. British Journal of Cancer. 70: 684-9. PMID 7917918 DOI: 10.1038/Bjc.1994.373 |
0.328 |
|
1994 |
van der Drift P, Chan A, van Roy N, Laureys G, Westerveld A, Speleman F, Versteeg R. A multimegabase cluster of snRNA and tRNA genes on chromosome 1p36 harbours an adenovirus/SV40 hybrid virus integration site. Human Molecular Genetics. 3: 2131-6. PMID 7881409 DOI: 10.1093/Hmg/3.12.2131 |
0.39 |
|
1994 |
Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Analysis of mutations in the SCH gene in schwannomas. Genes, Chromosomes & Cancer. 11: 7-14. PMID 7529050 DOI: 10.1002/Gcc.2870110103 |
0.318 |
|
1994 |
Bijlsma EK, Leenstra S, Westerveld A, Bosch DA, Hulsebos TJ. Amplification of the anonymous marker D17S67 in malignant astrocytomas. Genes, Chromosomes & Cancer. 9: 148-52. PMID 7513547 DOI: 10.1002/Gcc.2870090213 |
0.386 |
|
1994 |
Ngan Ching C, Caron H, Chan A, Beitsma M, van Sluis P, Speleman F, Westerveld A, Versteeg R. N-myc regulation in neuroblastoma Cancer Genetics and Cytogenetics. 77: 175. DOI: 10.1016/0165-4608(94)90335-2 |
0.459 |
|
1994 |
van der Drift P, Chan A, van Roy N, Laureys G, Westerveld A, Speleman F, Versteeg R. Analysis of a balanced translocation on chromosome 1p36 in a neuroblastoma patient Cancer Genetics and Cytogenetics. 77: 174. DOI: 10.1016/0165-4608(94)90334-4 |
0.369 |
|
1994 |
Alders M, Bliek J, Redeker E, Hoovers J, Feinberg A, Little P, Westerveld A, Mannens M. Characterization of the chromosomal regions involved in the Beckwith-Wiedemann syndrome Cancer Genetics and Cytogenetics. 77: 168. DOI: 10.1016/0165-4608(94)90309-3 |
0.357 |
|
1994 |
Redeker E, Hoovers J, Alders M, Bliek J, de Galan L, Feinberg A, Little P, Westerveld A, Mannens M. A physical map of the short arm of chromosome 11 involved in childhood solid tumours and the Beckwith-Wiedemann syndrome Cancer Genetics and Cytogenetics. 77: 168. DOI: 10.1016/0165-4608(94)90307-7 |
0.328 |
|
1993 |
Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members. Genomics. 15: 525-9. PMID 8468047 DOI: 10.1006/Geno.1993.1104 |
0.426 |
|
1993 |
Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nature Genetics. 4: 187-90. PMID 8102298 DOI: 10.1038/Ng0693-187 |
0.712 |
|
1993 |
Bijlsma EK, Delattre O, Juyn JA, Melot T, Westerveld A, Dumanski JP, Thomas G, Hulsebos TJ. Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2. Genes, Chromosomes & Cancer. 8: 112-8. PMID 7504514 DOI: 10.1002/Gcc.2870080208 |
0.404 |
|
1993 |
Caron H, Sluis Pv, Hoeve Mv, Kraker Jd, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Erratum: Corrigendum: Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification Nature Genetics. 4: 431-431. DOI: 10.1038/Ng0893-431A |
0.561 |
|
1992 |
Hoovers JM, Mannens M, John R, Bliek J, van Heyningen V, Porteous DJ, Leschot NJ, Westerveld A, Little PF. High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered. Genomics. 12: 254-63. PMID 1740334 DOI: 10.1016/0888-7543(92)90372-Y |
0.433 |
|
1992 |
Bijlsma EK, Brouwer-Mladin R, Bosch DA, Westerveld A, Hulsebos TJ. Molecular characterization of chromosome 22 deletions in schwannomas. Genes, Chromosomes & Cancer. 5: 201-5. PMID 1384671 DOI: 10.1002/Gcc.2870050305 |
0.351 |
|
1992 |
Versteeg R, Caron H, van Sluis P, Chan A, van Roy N, Cheng NC, Mannens M, Laurey G, Slater R, Speleman F, Westerveld A. Tumor suppressor genes in neuroblastoma Cancer Genetics and Cytogenetics. 63: 169. DOI: 10.1016/0165-4608(92)90516-B |
0.499 |
|
1991 |
Hulsebos TJ, Bijlsma EK, Geurts van Kessel AH, Brakenhoff RH, Westerveld A. Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2. Cytogenetics and Cell Genetics. 56: 171-5. PMID 2055112 DOI: 10.1159/000133080 |
0.383 |
|
1991 |
Mannens M, Hoovers JMN, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heynigen V, Junien C, Haber D, Speleman F, Heyting C, Slater RM, Leschot NJ, ... Westerveld A, et al. The distal region of 11p13 and associated genetic diseases Genomics. 11: 284-293. PMID 1769647 DOI: 10.1016/0888-7543(91)90134-Z |
0.357 |
|
1991 |
Hulsebos TJ, Oostra BA, Broersen S, Smits A, van Oost BA, Westerveld A. New distal marker closely linked to the fragile X locus. Human Genetics. 87: 369-72. PMID 1677926 DOI: 10.1007/Bf00200922 |
0.335 |
|
1991 |
Devilee P, van den Broek M, Mannens M, Slater R, Cornelisse CJ, Westerveld A, Khan PM. Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood. International Journal of Cancer. Journal International Du Cancer. 47: 817-21. PMID 1672665 DOI: 10.1002/Ijc.2910470604 |
0.343 |
|
1990 |
Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. Progress in Clinical and Biological Research. 321: 545-58. PMID 2183242 |
0.629 |
|
1990 |
Troelstra C, Odijk H, de Wit J, Westerveld A, Thompson LH, Bootsma D, Hoeijmakers JH. Molecular cloning of the human DNA excision repair gene ERCC-6. Molecular and Cellular Biology. 10: 5806-13. PMID 2172786 DOI: 10.1128/Mcb.10.11.5806 |
0.587 |
|
1990 |
Weeda G, van Ham RC, Masurel R, Westerveld A, Odijk H, de Wit J, Bootsma D, van der Eb AJ, Hoeijmakers JH. Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Molecular and Cellular Biology. 10: 2570-81. PMID 2111438 DOI: 10.1128/Mcb.10.6.2570 |
0.615 |
|
1990 |
BRUL S, WIEMER E, WESTERVELD A, STRIJLAND A, WANDERS R, TAGER J, SLATER E. A simple selection procedure for cells deficient in peroxisomes Cell Biology International Reports. 14: 64. DOI: 10.1016/0309-1651(90)90363-4 |
0.617 |
|
1990 |
Tager JM, Brul S, Wiemer EAC, Heikoop JC, Middelkoop E, Bout A, Westerveld A, Wanders RJA. Peroxisomal disorders: An updating Adrenoleukodystrophy and Other Peroxisomal Disorders. Clinical, Biochemical, Genetic and Therapeutic Aspects: Proceedings of the International Workshop. Ics898. 3-15. |
0.552 |
|
1989 |
van Duin M, Vredeveldt G, Mayne LV, Odijk H, Vermeulen W, Klein B, Weeda G, Hoeijmakers JH, Bootsma D, Westerveld A. The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. Mutation Research. 217: 83-92. PMID 2918869 DOI: 10.1016/0921-8777(89)90059-1 |
0.594 |
|
1989 |
Bout A, Hoovers JM, Bakker E, Mannens MM, Geurts van Kessel A, Westerveld A, Tager JM, Benne R. Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23. Cytogenetics and Cell Genetics. 52: 147-50. PMID 2630187 DOI: 10.1159/000132865 |
0.605 |
|
1989 |
Thompson LH, Bachinski LL, Stallings RL, Dolf G, Weber CA, Westerveld A, Siciliano MJ. Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics. 5: 670-9. PMID 2591959 DOI: 10.1016/0888-7543(89)90107-9 |
0.458 |
|
1989 |
Mannens M, Bleeker-Wagemakers EM, Bliek J, Hoovers J, Mandjes I, van Tol S, Frants RR, Heyting C, Westerveld A, Slater RM. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenetics and Cell Genetics. 52: 32-6. PMID 2575483 DOI: 10.1159/000132834 |
0.357 |
|
1989 |
Darroudi F, Westerveld A, Natarajan AT. Cytogenetical characterisation of Chinese hamster 43-3B transferants with the amplified or non-amplified human DNA repair gene ERCC-1. Mutation Research. 212: 113-22. PMID 2499774 DOI: 10.1016/0027-5107(89)90062-6 |
0.384 |
|
1988 |
Brul S, Wiemer EA, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, Van den Bosch H, Tager JM. Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders. Biochemical and Biophysical Research Communications. 152: 1083-9. PMID 3377768 DOI: 10.1016/S0006-291X(88)80395-4 |
0.638 |
|
1988 |
van Duin M, Janssen JH, de Wit J, Hoeijmakers JH, Thompson LH, Bootsma D, Westerveld A. Transfection of the cloned human excision repair gene ERCC-1 to UV-sensitive CHO mutants only corrects the repair defect in complementation group-2 mutants. Mutation Research. 193: 123-30. PMID 3347205 DOI: 10.1016/0167-8817(88)90042-9 |
0.566 |
|
1988 |
van Duin M, van den Tol J, Warmerdam P, Odijk H, Meijer D, Westerveld A, Bootsma D, Hoeijmakers JH. Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. Nucleic Acids Research. 16: 5305-22. PMID 3290851 DOI: 10.1093/Nar/16.12.5305 |
0.56 |
|
1988 |
Bootsma D, Westerveld A, Hoeijmakers JH. DNA repair in human cells: from genetic complementation to isolation of genes. Cancer Surveys. 7: 303-15. PMID 3066477 |
0.537 |
|
1988 |
Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. The Journal of Clinical Investigation. 81: 1710-5. PMID 2454948 DOI: 10.1172/Jci113510 |
0.653 |
|
1987 |
van Duin M, Koken MH, van den Tol J, ten Dijke P, Odijk H, Westerveld A, Bootsma D, Hoeijmakers JH. Genomic characterization of the human DNA excision repair gene ERCC-1. Nucleic Acids Research. 15: 9195-213. PMID 3684592 DOI: 10.1093/Nar/15.22.9195 |
0.556 |
|
1987 |
Keijzer W, Stefanini M, Bootsma D, Verkerk A, Geurts van Kessel AH, Jongkind JF, Westerveld A. Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1. Experimental Cell Research. 169: 490-501. PMID 3556430 DOI: 10.1016/0014-4827(87)90209-6 |
0.647 |
|
1987 |
Hoeijmakers JH, Odijk H, Westerveld A. Differences between rodent and human cell lines in the amount of integrated DNA after transfection. Experimental Cell Research. 169: 111-9. PMID 3028842 DOI: 10.1016/0014-4827(87)90230-8 |
0.356 |
|
1987 |
Zdzienicka MZ, Roza L, Westerveld A, Bootsma D, Simons JW. Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line. Mutation Research. 183: 69-74. PMID 3025723 DOI: 10.1016/0167-8817(87)90047-2 |
0.549 |
|
1987 |
Zdzienicka M, Westerveld A, Simons J, Bootsma D. Biological and biochemical consequences of the human ERCC1 repair gene in a repair-deficient Chinese hamster ovary cell line Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 181: 353. DOI: 10.1016/0027-5107(87)90206-5 |
0.536 |
|
1986 |
Arwert F, Porck HJ, Fràter-Schröder M, Brahe C, Geurts van Kessel A, Westerveld A, Meera Khan P, Zang K, Frants RR, Kortbeek HT. Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells. Human Genetics. 74: 378-81. PMID 3466852 DOI: 10.1007/Bf00280489 |
0.445 |
|
1986 |
Hoeijmakers JH, van Duin M, Westerveld A, Yasui A, Bootsma D. Identification of DNA repair genes in the human genome. Cold Spring Harbor Symposia On Quantitative Biology. 51: 91-101. PMID 3034490 DOI: 10.1101/Sqb.1986.051.01.012 |
0.553 |
|
1986 |
van Duin M, de Wit J, Odijk H, Westerveld A, Yasui A, Koken MH, Hoeijmakers JH, Bootsma D. Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. Cell. 44: 913-23. PMID 2420469 DOI: 10.1016/0092-8674(86)90014-0 |
0.584 |
|
1985 |
Stefanini M, Keijzer W, Westerveld A, Bootsma D. Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells. Experimental Cell Research. 161: 373-80. PMID 4065224 DOI: 10.1016/0014-4827(85)90094-1 |
0.563 |
|
1985 |
Sips HJ, de Wit-Verbeek HA, de Wit J, Westerveld A, Galjaard H. The chromosomal localization of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22. Human Genetics. 69: 340-4. PMID 3921454 DOI: 10.1007/Bf00291653 |
0.348 |
|
1984 |
Westerveld A, Hoeijmakers JH, van Duin M, de Wit J, Odijk H, Pastink A, Wood RD, Bootsma D. Molecular cloning of a human DNA repair gene. Nature. 310: 425-9. PMID 6462228 DOI: 10.1038/310425A0 |
0.58 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 7 of 11) Cytogenetic and Genome Research. 37: 525-545. DOI: 10.1159/000316931 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 11 of 11) Cytogenetic and Genome Research. 37: 609-616. DOI: 10.1159/000316928 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 10 of 11) Cytogenetic and Genome Research. 37: 588-608. DOI: 10.1159/000316927 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 9 of 11) Cytogenetic and Genome Research. 37: 567-587. DOI: 10.1159/000316926 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 8 of 11) Cytogenetic and Genome Research. 37: 546-566. DOI: 10.1159/000316925 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 6 of 11) Cytogenetic and Genome Research. 37: 504-524. DOI: 10.1159/000316924 |
0.521 |
|
1984 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Contents, Vol. 37, 1984 Cytogenetic and Genome Research. 37. DOI: 10.1159/000132002 |
0.479 |
|
1983 |
Barneveld RA, Keijzer W, Tegelaers FP, Ginns EI, Geurts van Kessel A, Brady RO, Barranger JA, Tager JM, Galjaard H, Westerveld A, Reuser AJ. Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies. Human Genetics. 64: 227-31. PMID 6885065 DOI: 10.1007/Bf00279398 |
0.575 |
|
1982 |
de Jonge AJ, Abrahams PJ, Westerveld A, Bootsma D. Expression of human hprt gene on the inactive X chromosome after DNA-mediated gene transfer. Nature. 295: 624-6. PMID 7199123 DOI: 10.1038/295624A0 |
0.628 |
|
1982 |
Ruddle FH, Bootsma D, Stefani M, Keijzer W, Westerveld A, Van Cong N, Weil D, Hors-Cayla MC, Gross MS, Heuertz S, Foubert C, Frézal J, Solomon E, Shows TB, Sakaguchi AY, et al. Workshop on mapping by somatic cell hybridization. Progress in Clinical and Biological Research. 103: 145-53. PMID 7163192 |
0.503 |
|
1982 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 1 of 11) Cytogenetic and Genome Research. 32: 247-267. PMID 7140367 DOI: 10.1159/000131703 |
0.521 |
|
1982 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 2 of 11) Cytogenetic and Genome Research. 32: 268-288. DOI: 10.1159/000316914 |
0.521 |
|
1982 |
McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Subject Index Vol. 32, 1982 Cytogenetic and Genome Research. 32: 338-341. DOI: 10.1159/000131706 |
0.48 |
|
1982 |
McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Contents, Vol. 32, 1982 Cytogenetic and Genome Research. 32. DOI: 10.1159/000131683 |
0.479 |
|
1982 |
McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Peter John Langford Cook, BA, MB Cantab., PhD Lond. Cytogenetic and Genome Research. 32: 5-6. DOI: 10.1159/000131681 |
0.503 |
|
1981 |
De Groot PG, Ovde Elferink RO, Hollemans M, Strijland A, Westerveld A, Meera Khan P, Tager JM. Inactivation by chloroquine of alpha-galactosidase in cultured human skin fibroblasts. Experimental Cell Research. 136: 327-33. PMID 6273196 DOI: 10.1016/0014-4827(81)90011-2 |
0.605 |
|
1980 |
Geurts van Kessel AH, Westerveld A, de Groot PG, Meera Khan P, Hagemeijer A. Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22. Cytogenetics and Cell Genetics. 28: 169-72. PMID 7192199 DOI: 10.1159/000131527 |
0.574 |
|
1980 |
Müller CR, Westerveld A, Migl B, Franke W, Ropers HH. Regional assignment of the gene locus for steroid sulfatase. Human Genetics. 54: 201-4. PMID 6985463 DOI: 10.1007/BF00278972 |
0.339 |
|
1980 |
Hoeksema HL, De Wit J, Westerveld A. The genetic defect in the various types of human beta-galactosidase deficiency. Human Genetics. 53: 241-7. PMID 6766901 DOI: 10.1007/Bf00273505 |
0.423 |
|
1980 |
Suárez HG, Persuy MA, Westerveld A, Ermonval M, Kay A, Cassingena R. Linkage relationship between TK and SV40 T-antigen genes in the SV40-transformed WI98VaD human cell line. Experimental Cell Research. 129: 127-32. PMID 6253304 DOI: 10.1016/0014-4827(80)90337-7 |
0.389 |
|
1980 |
de Groot PG, Strijland A, Kalsbeek R, Meera Khan P, Westerveld A, Hamers MN, Tager JM. Effect of 2-deoxyglucose on lysosomal enzymes in cultured human skin fibroblasts. Experimental Cell Research. 126: 207-16. PMID 6244168 DOI: 10.1016/0014-4827(80)90487-5 |
0.598 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Catalog of mapped human gene markers Cytogenetic and Genome Research. 25: 3-8. PMID 295267 DOI: 10.1159/000131393 |
0.561 |
|
1979 |
de Wit J, Hoeksema HL, Bootsma D, Westerveld A. Assignment of structural beta-galactosidase loci to human chromosomes 3 and 22. Human Genetics. 51: 259-67. PMID 116956 DOI: 10.1007/Bf00283392 |
0.596 |
|
1979 |
Meager A, Graves HE, Walker JR, Burke DC, Swallow DM, Westerveld A. Somatic cell genetics of human interferon production in human-rodent cell hybrids. The Journal of General Virology. 45: 309-21. PMID 94346 DOI: 10.1099/0022-1317-45-2-309 |
0.332 |
|
1979 |
Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 4 of 11) Cytogenetic and Genome Research. 37: 462-482. DOI: 10.1159/000316922 |
0.521 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 5 of 11) Cytogenetic and Genome Research. 25: 205-221. DOI: 10.1159/000316912 |
0.521 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 3 of 11) Cytogenetic and Genome Research. 25: 170-190. DOI: 10.1159/000316910 |
0.521 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 2 of 5) Cytogenetic and Genome Research. 25: 149-169. DOI: 10.1159/000316909 |
0.521 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Subject Index Vol. 25, 1979 Cytogenetic and Genome Research. 25: 232-236. DOI: 10.1159/000131409 |
0.48 |
|
1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Contents, Vol. 25, 1979 Cytogenetic and Genome Research. 25. DOI: 10.1159/000131395 |
0.479 |
|
1978 |
Herbschleb-Voogt E, Monteba-van Heuvel M, Wijnen LM, Westerveld A, Pearson PL, Meera Khan P. Chromosomal assignment and regional localization of CS, ENO2, GAPDH, LDHB, PEPB, and TPI in man-rodent cell hybrids. Cytogenetics and Cell Genetics. 22: 482-6. PMID 318158 DOI: 10.1159/000131003 |
0.398 |
|
1978 |
de Groot PG, Westerveld A, Meera Khan P, Tager JM. Localization of a gene for human alpha-galactosidase B (= n-acetyl-alpha-d-galactosaminidase) on chromosome 22. Human Genetics. 44: 305-12. PMID 215508 DOI: 10.1007/Bf00394295 |
0.642 |
|
1978 |
Garver JJ, Pearson PL, Estop A, Dijksman TM, Wijnen LMM, Westerveld A, Khan PM. Gene assignments to the presumptive homologs of human chromosomes 1, 6,11,12, and X in the Pongidae and Cercopithecoidea Cytogenetic and Genome Research. 22: 564-569. PMID 110528 DOI: 10.1159/000131024 |
0.414 |
|
1978 |
de Groot PG, Hamers MN, Westerveld A, Schram AW, Meera Khan P, Tager JM. A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids. Human Genetics. 44: 295-304. PMID 83282 DOI: 10.1007/Bf00394294 |
0.637 |
|
1978 |
Bootsma D, Ruddle FH, Aitken DA, Brown JA, Bruns GAP, Chu EHY, Croce CM, Craig IW, Francke U, Gedde-Dahl T, George DL, German JL, Grzeschik KH, Hellkuhl B, Jones CA, ... ... Westerveld A, et al. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, 5, 7, 8, 10, 11, and 12 Cytogenetic and Genome Research. 22: 74-91. DOI: 10.1159/000130919 |
0.535 |
|
1977 |
De Wit J, Hoeksema HL, Halley D, Hagemeijer A, Bootsma D, Westerveld A. Regional localization of a beta-galactosidase locus on human chromosome 22. Somatic Cell Genetics. 3: 351-63. PMID 414365 DOI: 10.1007/Bf01542965 |
0.606 |
|
1977 |
Hoeksema HL, Reuser AJJ, Hoogeveen AT, Westerveld A, Galjaard H. Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids Human Genetics. 39: 315-319. PMID 413781 DOI: 10.1007/Bf00295426 |
0.344 |
|
1977 |
Hamers MN, Westerveld A, Khan M, Tager JM. Characterization of α-galactosidase isoenzymes in normal and fabry human-Chinese hamster somatic cell hybrids Human Genetics. 36: 289-297. PMID 404232 DOI: 10.1007/Bf00446279 |
0.541 |
|
1976 |
Wullems G, Van der Horst J, Westerveld A, Bootsma D. Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. Birth Defects Original Article Series. 12: 409-11. PMID 1024646 |
0.569 |
|
1976 |
Wullems G, van der Horst J, Westerveld A, Bootsma D. Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. Cytogenetics and Cell Genetics. 16: 409-11. PMID 975919 DOI: 10.1159/000130645 |
0.569 |
|
1976 |
Meera Khan P, Pearson PL, Wijnen LL, Doppert BA, Westerveld A, Bootsma D. Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Birth Defects Original Article Series. 12: 420-1. PMID 828864 |
0.598 |
|
1976 |
Westerveld A, Jongsma AP, Meera Khan P, Someren H, Bootsma D. Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. Birth Defects Original Article Series. 12: 247-51. PMID 192371 |
0.596 |
|
1976 |
Meera Khan P, Pearson PL, Wijnen LL, Doppert BA, Westerveld A, Bootsma D. Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 420-1. PMID 185023 DOI: 10.1159/000130648 |
0.639 |
|
1976 |
Westerveld A, Jongsma AP, Meera Khan P, van Someren H, Bootsma D. Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 247-51. PMID 185020 DOI: 10.1159/000130603 |
0.637 |
|
1976 |
Westerveld A, Jongsma AP, Meera Khan P, van Someren H, Bootsma D. Assignment of the AK1:Np:ABO linkage group to human chromosome 9. Proceedings of the National Academy of Sciences of the United States of America. 73: 895-9. PMID 176661 DOI: 10.1073/Pnas.73.3.895 |
0.612 |
|
1975 |
De Wit J, Bootsma D, Pearson PL, Westerveld A. Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. Cytogenetics and Cell Genetics. 15: 129-37. PMID 1238234 DOI: 10.1159/000130511 |
0.591 |
|
1975 |
Westerveld A, Van Someren H, Beyersbergen Van Henegouwen and Oosterbaan HMARA. Synteny relationship between the human loci for hexosaminidase A, mannose phosphate isomerase, and pyruvate kinase 3 studied in man Chinese hamster somatic cell hybrids Birth Defects: Original Article Series. 11: 285-287. PMID 1203498 DOI: 10.1159/000130406 |
0.37 |
|
1975 |
Westerveld A, Beyersbergen Van Henegouwen HMA, Van Someren H. Evidence for synteny between the human loci for galactose 1 phosphate uridyl transferase and aconitase in man Chinese hamster somatic cell hybrids Birth Defects: Original Article Series. 11: 283-284. PMID 1203497 |
0.304 |
|
1975 |
Westerveld A, Beyersbergen van Henegouwen HM, van Someren H. Evidence for synteny between the human loci for galactose-1-phosphate uridyl transferase and aconitase in man-Chinese hamster somatic cell hybrids Cytogenetics and Cell Genetics. 14: 453-454. PMID 1192837 DOI: 10.1159/000130405 |
0.418 |
|
1975 |
Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. Cytogenetics and Cell Genetics. 14: 375-80. PMID 1192822 DOI: 10.1159/000130389 |
0.548 |
|
1975 |
Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. Birth Defects Original Article Series. 11: 205-10. PMID 812566 |
0.497 |
|
1975 |
Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. α-Galactosidase in man-Chinese hamster somatic cell hybrids Cytogenetic and Genome Research. 14: 205-210. DOI: 10.1159/000130389 |
0.508 |
|
1974 |
van Someren H, Kahn PM, Westerveld A, Bootsma D. Claim that two human linkage groups carry different loci for GPT and LDH withdrawn. Nature. 249: 279-80. PMID 4833247 DOI: 10.1038/249279A0 |
0.621 |
|
1974 |
van Someren H, van Henegouwen HB, Westerveld A, Bootsma D. Synteny of the human loci for fumarate hydratase and UDPG pyrophosphorylase with chromosome 1 markers in somatic cell hybrids Cytogenetic and Genome Research. 13: 551-557. PMID 4549862 DOI: 10.1159/000130306 |
0.631 |
|
1974 |
Galjaard H, Hoogeveen A, de Wit-Verbeek HA, Reuser AJ, Keijzer W, Westerveld A, Bootsma D. Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization. Experimental Cell Research. 87: 444-8. PMID 4416048 DOI: 10.1016/0014-4827(74)90515-1 |
0.563 |
|
1974 |
Khan PM, Los WRT, Los WR, Pearson PL, Westerveld A, Bootsma D. Genetical studies on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids Human Heredity. 24: 415-423. PMID 4377261 DOI: 10.1159/000152700 |
0.611 |
|
1974 |
Khan PM, Doppert BA, Hagemeijer A, Westerveld A. The human loci for phosphopyruvate hydratase and guanylate kinase are syntenic with the PGD-PGM1 linkage group in man-chinese hamster somatic cell hybrids Cytogenetic and Genome Research. 13: 130-131. PMID 4363865 DOI: 10.1159/000130255 |
0.381 |
|
1974 |
van Someren H, Westerveld A, Hagemeijer A, Mees JR, Meera Khan P, Zaalberg OB. Human antigen and enzyme markers in man; Chinese hamster somatic cell hybrids: evidence for synteny between the HL A, PGM 3, ME 1, and IPO B loci Proceedings of the National Academy of Sciences of the United States of America. 71: 962-965. PMID 4362641 DOI: 10.1073/Pnas.71.3.962 |
0.381 |
|
1974 |
Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Human Genetic Mutant Cell Repository Index / Book Review Index Cytogenetic and Genome Research. 13: 584-584. DOI: 10.1159/000130310 |
0.545 |
|
1974 |
Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Subject Index Vol. 13, 1974 Cytogenetic and Genome Research. 13: 581-583. DOI: 10.1159/000130309 |
0.48 |
|
1974 |
Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Contents, Vol. 13, 1974 Cytogenetic and Genome Research. 13. DOI: 10.1159/000130302 |
0.479 |
|
1973 |
Jongsma A, van Someren H, Westerveld A, Hagemeijer A, Pearson P. Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids - Assignment of PGM3 to chromosome C6 and regional mapping of the PGD, PGM1 and Pep-C genes on chromosome A1 Humangenetik. 20: 195-202. PMID 4358963 DOI: 10.1007/Bf00385730 |
0.44 |
|
1972 |
Westerveld A, Visser RPLS, Freeke MA, Bootsma D. Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase, and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity Biochemical Genetics. 7: 33-40. PMID 5064956 DOI: 10.1007/Bf00487007 |
0.533 |
|
1972 |
Westerveld A, Khan PM. Evidence for linkage between human loci for 6-phosphogluconate dehydrogenase and phosphoglucomutase1 in man-Chinese hamster somatic cell hybrids Nature. 236: 30-32. PMID 4553635 DOI: 10.1038/236030A0 |
0.446 |
|
1972 |
van Someren H, Meera Khan P, Westerveld A, Bootsma D. Two new linkage groups in man, both carrying different loci for lactate dehydrogenase and glutamic-pyruvic transaminase Nature: New Biology. 240: 221-223. PMID 4509147 DOI: 10.1038/Newbio240221A0 |
0.643 |
|
1972 |
Grzeschik KH, Grzeschik AM, Banhof S, Romeo G, Siniscalco M, van Someren H, Meera Khan P, Westerveld A, Bootsma D. X-linkage of human -galactosidase Nature: New Biology. 240: 48-50. PMID 4508394 DOI: 10.1038/Newbio240048A0 |
0.546 |
|
1971 |
Westerveld A, Visser RP, Meera Khan P, Bootsma D. Loss of human genetic markers in man--Chinese hamster somatic cell hybrids Nature: New Biology. 234: 20-24. PMID 5286856 DOI: 10.1038/Newbio234020A0 |
0.635 |
|
Show low-probability matches. |