| Year |
Citation |
Score |
| 2004 |
Stitziel NO, Mar BG, Liang J, Westbrook CA. Membrane-associated and secreted genes in breast cancer. Cancer Research. 64: 8682-7. PMID 15574777 DOI: 10.1158/0008-5472.Can-04-1729 |
0.591 |
|
| 2002 |
Gomes I, Sharma TT, Edassery S, Fulton N, Mar BG, Westbrook CA. Novel transcription factors in human CD34 antigen-positive hematopoietic cells. Blood. 100: 107-19. PMID 12070015 DOI: 10.1182/Blood.V100.1.107 |
0.356 |
|
| 2001 |
Hu Z, Gomes I, Horrigan SK, Kravarusic J, Mar B, Arbieva Z, Chyna B, Fulton N, Edassery S, Raza A, Westbrook CA. A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31. Oncogene. 20: 6946-54. PMID 11687974 DOI: 10.1038/Sj.Onc.1204850 |
0.455 |
|
| 2001 |
Gomes I, Sharma TT, Mahmud N, Kapp JD, Edassery S, Fulton N, Liang J, Hoffman R, Westbrook CA. Highly abundant genes in the transcriptosome of human and baboon CD34 antigen-positive bone marrow cells. Blood. 98: 93-9. PMID 11418467 DOI: 10.1182/Blood.V98.1.93 |
0.354 |
|
| 2001 |
Westbrook C, Gomes I, Le T, Kapp J, Hoffman R. A cDNA data set for expression studies of hematopoietic stem cells: characterization and database mining Nature Genetics. 27: 95-95. DOI: 10.1038/87360 |
0.342 |
|
| 2001 |
Arbieva Z, Banerjee K, Usha L, Le T, Gomes I, Westbrook C. Identification of downstream targets of the putative tumor suppressor gene on 8p by differential gene expression analysis Nature Genetics. 27: 40-40. DOI: 10.1038/86984 |
0.347 |
|
| 2000 |
Xie H, Hu Z, Chyna B, Horrigan SK, Westbrook CA. Human mortalin (HSPA9): a candidate for the myeloid leukemia tumor suppressor gene on 5q31. Leukemia. 14: 2128-34. PMID 11187902 DOI: 10.1038/Sj.Leu.2401935 |
0.45 |
|
| 2000 |
Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, ... ... Westbrook CA, et al. Myotilin is mutated in limb girdle muscular dystrophy 1A. Human Molecular Genetics. 9: 2141-7. PMID 10958653 DOI: 10.1093/Hmg/9.14.2141 |
0.323 |
|
| 2000 |
Arbieva ZH, Banerjee K, Kim SY, Edassery SL, Maniatis VS, Horrigan SK, Westbrook CA. High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22. Genome Research. 10: 244-57. PMID 10673282 DOI: 10.1101/Gr.10.2.244 |
0.303 |
|
| 2000 |
Horrigan SK, Arbieva ZH, Xie HY, Kravarusic J, Fulton NC, Naik H, Le TT, Westbrook CA. Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31. Blood. 95: 2372-2377. DOI: 10.1182/Blood.V95.7.2372.007K20_2372_2377 |
0.497 |
|
| 2000 |
Westbrook CA, Hu Z, Arbieva Z, Kravarusic J, Chyna B, Edassery S, Horrigan SK. Novel nuclear receptor coactivator is a candidate for the del(5q) Leukemia tumor suppressor gene Experimental Hematology. 28: 1492. DOI: 10.1016/S0301-472X(00)00656-1 |
0.45 |
|
| 2000 |
Le TT, Gomes I, Liang J, Turpaz Y, Sharma AK, Nelson MC, Hoffman R, Westbrook CA. Comparability of gene expression between human and baboon CD34+ marrow cells Experimental Hematology. 28: 58-59. DOI: 10.1016/S0301-472X(00)00271-X |
0.375 |
|
| 1999 |
Horrigan SK, Bartoloni L, Speer MC, Fulton N, Kravarusic J, Ramesar R, Vance JM, Yamaoka LH, Westbrook CA. A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences. Genomics. 57: 24-35. PMID 10191080 DOI: 10.1006/Geno.1999.5765 |
0.415 |
|
| 1998 |
Bartoloni L, Horrigan SK, Viles KD, Gilchrist JM, Stajich JM, Vance JM, Yamaoka LH, Pericak-Vance MA, Westbrook CA, Speer MC. Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31. Genomics. 54: 250-5. PMID 9828127 DOI: 10.1006/Geno.1998.5579 |
0.373 |
|
| 1998 |
Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families. Human Heredity. 48: 179-84. PMID 9694248 DOI: 10.1159/000022799 |
0.312 |
|
| 1998 |
Kim SY, Horrigan SK, Altenhofen JL, Arbieva ZH, Hoffman R, Westbrook CA. Modification of bacterial artificial chromosome clones using Cre recombinase: introduction of selectable markers for expression in eukaryotic cells. Genome Research. 8: 404-12. PMID 9548976 DOI: 10.1101/Gr.8.4.404 |
0.39 |
|
| 1997 |
Zeremski M, Horrigan SK, Grigorian IA, Westbrook CA, Gudkov AV. Localization of the candidate tumor suppressor gene ING1 to human chromosome 13q34. Somatic Cell and Molecular Genetics. 23: 233-6. PMID 9330636 DOI: 10.1007/Bf02721376 |
0.478 |
|
| 1997 |
Stock W, Westbrook CA, Peterson B, Arthur DC, Szatrowski TP, Silver RT, Sher DA, Wu D, Le Beau MM, Schiffer CA, Bloomfield CD. Value of molecular monitoring during the treatment of chronic myeloid leukemia: a Cancer and Leukemia Group B study. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 15: 26-36. PMID 8996121 DOI: 10.1200/Jco.1997.15.1.26 |
0.357 |
|
| 1997 |
Takanishijr D, Kim S, Kelemen P, Yaremko M, Kim A, Ramesar J, Horrigan S, Montag A, Michelassi F, Westbrook C. Chromosome 8 Losses in Colorectal Carcinoma: Localization and Correlation With Invasive Disease. Molecular Diagnosis. 2: 3-10. DOI: 10.1016/S1084-8592(97)80003-3 |
0.387 |
|
| 1996 |
Yaremko ML, Kutza C, Lyzak J, Mick R, Recant WM, Westbrook CA. Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer. Genes, Chromosomes & Cancer. 16: 189-95. PMID 8814452 DOI: 10.1002/(Sici)1098-2264(199607)16:3<189::Aid-Gcc6>3.0.Co;2-V |
0.346 |
|
| 1995 |
Takanishi DM, Angriman I, Yaremko ML, Montag A, Westbrook CA, Michelassi F. Chromosome 17p allelic loss in colorectal carcinoma. Clinical significance. Archives of Surgery (Chicago, Ill. : 1960). 130: 585-8; discussion 58. PMID 7763165 DOI: 10.1001/Archsurg.1995.01430060023005 |
0.405 |
|
| 1995 |
Yaremko ML, Recant WM, Westbrook CA. Loss of heterozygosity from the short arm of chromosome 8 is an early event in breast cancers. Genes, Chromosomes & Cancer. 13: 186-91. PMID 7669738 DOI: 10.1002/Gcc.2870130308 |
0.411 |
|
| 1995 |
Westbrook CA, Arenas RB. Gene therapy of the gut: introduction of the APC tumor-suppressor gene for cancer prevention or treatment Advanced Drug Delivery Reviews. 17: 349-355. DOI: 10.1016/0169-409X(95)00070-N |
0.361 |
|
| 1994 |
Westbrook CA, Le Beau MM, Neuman WL, Keinanen M, Yamaoka LH, Speer MC, Espinosa R, Nakamura Y, Williamson R, Mullan M. Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain. Cytogenetics and Cell Genetics. 67: 86-93. PMID 7913678 DOI: 10.1159/000133805 |
0.361 |
|
| 1994 |
Yamaoka LH, Westbrook CA, Speer MC, Gilchrist JM, Jabs EW, Schweins EG, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA. Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9. Neuromuscular Disorders : Nmd. 4: 471-5. PMID 7881291 DOI: 10.1016/0960-8966(94)90086-8 |
0.406 |
|
| 1994 |
Westbrook CA, Chmura SJ, Arenas RB, Kim SY, Otto G. Human APC gene expression in rodent colonic epithelium in vivo using liposomal gene delivery. Human Molecular Genetics. 3: 2005-10. PMID 7874118 DOI: 10.1093/Hmg/3.11.2005 |
0.371 |
|
| 1994 |
Kelemen PR, Yaremko ML, Kim AH, Montag A, Michelassi F, Westbrook CA. Loss of heterozygosity in 8p is associated with microinvasion in colorectal carcinoma. Genes, Chromosomes & Cancer. 11: 195-8. PMID 7530488 DOI: 10.1002/Gcc.2870110308 |
0.373 |
|
| 1994 |
Yaremko ML, Wasylyshyn ML, Paulus KL, Michelassi F, Westbrook CA. Deletion mapping reveals two regions of chromosome 8 allele loss in colorectal carcinomas. Genes, Chromosomes & Cancer. 10: 1-6. PMID 7519868 DOI: 10.1002/Gcc.2870100102 |
0.456 |
|
| 1994 |
Riggins GJ, Sherman SL, Phillips CN, Stock W, Westbrook CA, Warren ST. CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome. Genes, Chromosomes & Cancer. 9: 141-4. PMID 7513545 DOI: 10.1002/Gcc.2870090211 |
0.468 |
|
| 1993 |
Le Beau MM, Espinosa R, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proceedings of the National Academy of Sciences of the United States of America. 90: 5484-8. PMID 8516290 DOI: 10.1073/Pnas.90.12.5484 |
0.493 |
|
| 1993 |
Neuman WL, Westbrook CA, Dixon M, Espinosa R, Patel YD, Nakamura Y, Weiffenbach B, Le Beau MM. Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 62: 207-10. PMID 8095009 DOI: 10.1159/000133477 |
0.402 |
|
| 1992 |
Thangavelu M, Neuman WL, Espinosa R, Nakamura Y, Westbrook CA, Le Beau MM. A physical and genetic linkage map of the distal long arm of human chromosome 5. Cytogenetics and Cell Genetics. 59: 27-30. PMID 1733669 DOI: 10.1159/000133193 |
0.412 |
|
| 1992 |
Westbrook CA. The role of molecular techniques in the clinical management of leukemia. Lessons from the Philadelphia chromosome. Cancer. 70: 1695-700. PMID 1516023 DOI: 10.1002/1097-0142(19920915)70:4+<1695::Aid-Cncr2820701608>3.0.Co;2-D |
0.426 |
|
| 1992 |
Stock W, Chandrasekharappa SC, Neuman WL, Le Beau MM, Brownstein BH, Westbrook CA. Characterization of yeast artificial chromosomes containing interleukin genes on human chromosome 5. Cytogenetics and Cell Genetics. 61: 263-5. PMID 1486800 DOI: 10.1159/000133417 |
0.391 |
|
| 1992 |
Neuman WL, Le Beau MM, Farber RA, Lindgren V, Westbrook CA. Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis. Cytogenetics and Cell Genetics. 61: 103-6. PMID 1395713 DOI: 10.1159/000133381 |
0.46 |
|
| 1992 |
Westbrook CA, Keinänen MJ. Myeloid malignancies and chromosome 5 deletions. Bailliã¨Re's Clinical Haematology. 5: 931-42. PMID 1339191 DOI: 10.1016/S0950-3536(11)80052-1 |
0.496 |
|
| 1992 |
Westbrook CA, Hooberman AL, Spino C, Dodge RK, Larson RA, Davey F, Wurster-Hill DH, Sobol RE, Schiffer C, Bloomfield CD. Clinical significance of the BCR-ABL fusion gene in adult acute lymphoblastic leukemia: a Cancer and Leukemia Group B Study (8762) Blood. 80: 2983-2990. DOI: 10.1182/Blood.V80.12.2983.Bloodjournal80122983 |
0.43 |
|
| 1991 |
Westbrook CA, Neuman WL, Hewitt J, Kidd KK, Le Beau MM, Williamson R. Report of the chromosome 5 workshop. Genomics. 10: 1105-9. PMID 1916818 DOI: 10.1016/0888-7543(91)90211-V |
0.418 |
|
| 1991 |
Hanish J, Rebelsky M, McClelland M, Westbrook C. Application of methylase-limited partial NotI cleavage for a long-range restriction map of the human ABL locus. Genomics. 10: 681-5. PMID 1889813 DOI: 10.1016/0888-7543(91)90452-K |
0.326 |
|
| 1991 |
Neuman WL, Wasylyshyn ML, Jacoby R, Erroi F, Angriman I, Montag A, Brasitus T, Michelassi F, Westbrook CA. Evidence for a common molecular pathogenesis in colorectal, gastric, and pancreatic cancer. Genes, Chromosomes & Cancer. 3: 468-73. PMID 1663781 DOI: 10.1002/Gcc.2870030609 |
0.353 |
|
| 1990 |
Chandrasekharappa SC, Rebelsky MS, Firak TA, Le Beau MM, Westbrook CA. A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5. Genomics. 6: 94-9. PMID 2303264 DOI: 10.1016/0888-7543(90)90452-Z |
0.45 |
|
| 1990 |
Papadopoulos PC, Greenstein AM, Gaffney RA, Westbrook CA, Wiedemann LM. Characterization of the translocation breakpoint sequences in Philadelphia-positive acute lymphoblastic leukemia. Genes, Chromosomes & Cancer. 1: 233-9. PMID 2083218 DOI: 10.1002/Gcc.2870010308 |
0.399 |
|
| 1990 |
Becker MA, Heidler SA, Bell GI, Seino S, Le Beau MM, Westbrook CA, Neuman W, Shapiro LJ, Mohandas TK, Roessler BJ. Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes. Genomics. 8: 555-61. PMID 1962753 DOI: 10.1016/0888-7543(90)90043-T |
0.486 |
|
| 1989 |
Hooberman AL, Westbrook CA. Molecular Diagnosis of the Philadelphia Chromosome in Acute Lymphoblastic Leukemia. Leukemia & Lymphoma. 1: 3-10. PMID 27456401 DOI: 10.3109/10428198909042452 |
0.444 |
|
| 1989 |
Hooberman AL, Carrino JJ, Leibowitz D, Rowley JD, Le Beau MM, Arlin ZA, Westbrook CA. Unexpected heterogeneity of BCR-ABL fusion mRNA detected by polymerase chain reaction in Philadelphia chromosome-positive acute lymphoblastic leukemia. Proceedings of the National Academy of Sciences of the United States of America. 86: 4259-63. PMID 2498881 DOI: 10.1073/Pnas.86.11.4259 |
0.447 |
|
| 1989 |
Hooberman AL, Rubin CM, Barton KP, Westbrook CA. Detection of the Philadelphia chromosome in acute lymphoblastic leukemia by pulsed-field gel electrophoresis. Blood. 74: 1101-1107. DOI: 10.1182/Blood.V74.3.1101.1101 |
0.397 |
|
| 1988 |
Westbrook CA. The ABL oncogene in human leukemias. Blood Reviews. 2: 1-8. PMID 3289649 DOI: 10.1016/0268-960X(88)90002-1 |
0.446 |
|
| 1988 |
Rubin CM, Blazar BR, Hooberman AL, Dickler MN, Miller BA, Westbrook CA. A deletion/insertion polymorphism in the human BCR gene on chromosome 22. Nucleic Acids Research. 16: 8741. PMID 2901728 DOI: 10.1093/Nar/16.17.8741 |
0.459 |
|
| 1988 |
Rubin CM, Carrino JJ, Dickler MN, Leibowitz D, Smith SD, Westbrook CA. Heterogeneity of genomic fusion of BCR and ABL in Philadelphia chromosome-positive acute lymphoblastic leukemia. Proceedings of the National Academy of Sciences of the United States of America. 85: 2795-9. PMID 2833755 DOI: 10.1073/Pnas.85.8.2795 |
0.474 |
|
| 1988 |
Westbrook C, Rubin C, Carrino J, Le Beau M, Bernards A, Rowley J. Long-range mapping of the Philadelphia chromosome by pulsed-field gel electrophoresis Blood. 71: 697-702. DOI: 10.1182/Blood.V71.3.697.697 |
0.498 |
|
| 1987 |
Westbrook CA, Rubin CM, Le Beau MM, Kaminer LS, Smith SD, Rowley JD, Diaz MO. Molecular analysis of TCRB and ABL in a t(7;9)-containing cell line (SUP-T3) from a human T-cell leukemia. Proceedings of the National Academy of Sciences of the United States of America. 84: 251-5. PMID 3025859 DOI: 10.1073/Pnas.84.1.251 |
0.451 |
|
| 1987 |
Ackland S, Westbrook C, Diaz M, Beau ML, Rowley J. Evidence favoring lineage fidelity in acute nonlymphocytic leukemia: absence of immunoglobulin gene rearrangements in FAB types M4 and M5 Blood. 69: 87-91. DOI: 10.1182/Blood.V69.1.87.87 |
0.349 |
|
| 1986 |
Le Beau MM, Pettenati MJ, Lemons RS, Diaz MO, Westbrook CA, Larson RA, Sherr CJ, Rowley JD. Assignment of the GM-CSF, CSF-1, and FMS genes to human chromosome 5 provides evidence for linkage of a family of genes regulating hematopoiesis and for their involvement in the deletion (5q) in myeloid disorders. Cold Spring Harbor Symposia On Quantitative Biology. 51: 899-909. PMID 3495397 DOI: 10.1101/Sqb.1986.051.01.103 |
0.452 |
|
| 1986 |
Le Beau MM, Westbrook CA, Diaz MO, Larson RA, Rowley JD, Gasson JC, Golde DW, Sherr CJ. Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders. Science (New York, N.Y.). 231: 984-7. PMID 3484837 DOI: 10.1126/Science.3484837 |
0.478 |
|
| 1985 |
Le Beau MM, Westbrook CA, Diaz MO, Rowley JD, Oren M. Translocation of the p53 gene in t(15;17) in acute promyelocytic leukaemia. Nature. 316: 826-8. PMID 3929142 DOI: 10.1038/316826A0 |
0.483 |
|
| 1985 |
Westbrook CA, Le Beau MM, Diaz MO, Groffen J, Rowley JD. Chromosomal localization and characterization of c-abl in the t(6;9) of acute nonlymphocytic leukemia. Proceedings of the National Academy of Sciences of the United States of America. 82: 8742-6. PMID 3866248 DOI: 10.1073/Pnas.82.24.8742 |
0.444 |
|
| 1985 |
Le Beau MM, Westbrook CA, Diaz MO, Rowley JD. c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proceedings of the National Academy of Sciences of the United States of America. 82: 6692-6. PMID 2413444 DOI: 10.1073/Pnas.82.19.6692 |
0.471 |
|
| 1984 |
Le Beau MM, Westbrook CA, Diaz MO, Rowley JD. Evidence for two distinct c-src loci on human chromosomes 1 and 20. Nature. 312: 70-1. PMID 6092965 DOI: 10.1038/312070A0 |
0.476 |
|
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