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Jianmin Chen, Ph.D. - Publications

Affiliations: 
2007 Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Genetics, Molecular Biology
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24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Chen J, Chen Y, Capizzi S, Yang M, Deng L, Bledsoe SB, Evan AP, Tischfield JA, Sahota A. 2,8-dihydroxyadenine nephrolithiasis induces developmental stage-specific alterations in gene expression in mouse kidney. Urology. 75: 914-22. PMID 20035974 DOI: 10.1016/J.Urology.2009.10.031  0.522
2009 Shao C, Liang L, Zhao X, Chen Y, Zheng B, Chen J, Luo M, Tischfield JA. Mutagenesis in vivo in T cells of p21-deficient mice. Mutation Research. 670: 103-6. PMID 19744501 DOI: 10.1016/J.Mrfmmm.2009.09.001  0.487
2006 Liang L, Chen J, Vittal R, Selvanayagam ZE, McAteer JA, Deng L, Tischfield J, Chin KV, Sahota A. Expression profiling of crystal-induced injury in human kidney epithelial cells. Nephron. Physiology. 103: p53-62. PMID 16374038 DOI: 10.1159/000090503  0.481
2005 Vernon HJ, Osborne C, Tzortzaki EG, Yang M, Chen J, Rittling SR, Denhardt DT, Buyske S, Bledsoe SB, Evan AP, Fairbanks L, Simmonds HA, Tischfield JA, Sahota A. Aprt/Opn double knockout mice: osteopontin is a modifier of kidney stone disease severity. Kidney International. 68: 938-47. PMID 16105024 DOI: 10.1111/J.1523-1755.2005.00487.X  0.629
1997 Chen J, Shao C, Lazar V, Srivastava CH, Lee WH, Tischfield JA. Localization of group IIc low molecular weight phospholipase A2 mRNA to meiotic cells in the mouse. Journal of Cellular Biochemistry. 64: 369-75. PMID 9057094 DOI: 10.1002/(SICI)1097-4644(19970301)64:3<369::AID-JCB3>3.0.CO;2-T  0.453
1996 Tischfield JA, Xia YR, Shih DM, Klisak I, Chen J, Engle SJ, Siakotos AN, Winstead MV, Seilhamer JJ, Allamand V, Gyapay G, Lusis AJ. Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and human. Genomics. 32: 328-33. PMID 8838795 DOI: 10.1006/Geno.1996.0126  0.432
1996 Engle SJ, Stockelman MG, Chen J, Boivin G, Yum MN, Davies PM, Ying MY, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA. Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis. Proceedings of the National Academy of Sciences of the United States of America. 93: 5307-12. PMID 8643571 DOI: 10.1073/Pnas.93.11.5307  0.468
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning and recombinant expression of a novel human low molecular weight Ca(2+)-dependent phospholipase A2. The Journal of Biological Chemistry. 269: 2365-8. PMID 8300559  0.44
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning and characterization of novel rat and mouse low molecular weight Ca(2+)-dependent phospholipase A2s containing 16 cysteines. The Journal of Biological Chemistry. 269: 23018-24. PMID 8083202  0.424
1994 Bye S, Mallmann R, Duley J, Simmonds HA, Chen J, Tischfield JA, Sahota A. Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasis. The Clinical Investigator. 72: 550-3. PMID 7981585 DOI: 10.1007/Bf00207486  0.511
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning, expression and partial characterization of a novel rat phospholipase A2. Biochimica Et Biophysica Acta. 1215: 115-20. PMID 7947992 DOI: 10.1016/0005-2760(94)90099-X  0.414
1994 Sahota A, Chen J, Boyadjiev SA, Gault MH, Tischfield JA. Missense mutation in the adenine phosphoribosyltransferase gene causing 2,8-dihydroxyadenine urolithiasis. Human Molecular Genetics. 3: 817-8. PMID 7915931  0.498
1994 Sahota A, Chen J, Bye S, Jaing J, Berenyi M, Fekete G, Tischfield JA. Occurrence of a missense mutation in one allele and a seven basepair deletion in the other allele in a patient with adenine phosphoribosyltransferase deficiency. Human Mutation. 3: 315-7. PMID 7912608 DOI: 10.1002/Humu.1380030324  0.493
1994 Sahota A, Bye S, Chen J, Khattar NH, Turker MS, Moro F, Simmonds HA, Emmerson BT, Gordon RB, Tischfield JA. Molecular characterization of a novel mutation in APRT heterozygotes. Advances in Experimental Medicine and Biology. 370: 675-8. PMID 7660994  0.489
1994 Bye S, Sahota A, Chen J, Tischfield JA. Analysis of APRT mutations by reverse-transcription PCR. Advances in Experimental Medicine and Biology. 370: 671-4. PMID 7660993  0.488
1993 Fye KH, Sahota A, Hancock DC, Gelb AB, Chen J, Sparks JW, Sibley RK, Tischfield JA. Adenine phosphoribosyltransferase deficiency with renal deposition of 2,8-dihydroxyadenine leading to nephrolithiasis and chronic renal failure. Archives of Internal Medicine. 153: 767-70. PMID 8447714  0.478
1993 Chen J, Sahota A, Martin GF, Hakoda M, Kamatani N, Stambrook PJ, Tischfield JA. Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: mutational hot spots at the intron 4 splice donor site and at codon 87. Mutation Research. 287: 217-25. PMID 7685481 DOI: 10.1016/0027-5107(93)90014-7  0.508
1991 Chen J, Sahota A, Stambrook PJ, Tischfield JA. Polymerase chain reaction amplification and sequence analysis of human mutant adenine phosphoribosyltransferase genes: the nature and frequency of errors caused by Taq DNA polymerase. Mutation Research. 249: 169-76. PMID 2067530 DOI: 10.1016/0027-5107(91)90143-C  0.448
1991 Sahota A, Chen J, Stambrook PJ, Tischfield JA. Mutational basis of adenine phosphoribosyltransferase deficiency. Advances in Experimental Medicine and Biology. 309: 73-6. PMID 1781410  0.507
1991 Chen J, Sahota A, Laxdal T, Scrine M, Bowman S, Cui C, Stambrook PJ, Tischfield JA. Identification of a single missense mutation in the adenine phosphoribosyltransferase (APRT) gene from five Icelandic patients and a British patient. American Journal of Human Genetics. 49: 1306-11. PMID 1746557  0.511
1991 Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PS, Tischfield JA, Zöllner N. A splice mutation at the adenine phosphoribosyltransferase locus detected in a German family. Advances in Experimental Medicine and Biology. 309: 83-6. PMID 1685862  0.465
1991 Sahota A, Chen J, Behzadian MA, Ravindra R, Takeuchi H, Stambrook PJ, Tischfield JA. 2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locus. American Journal of Human Genetics. 48: 983-9. PMID 1673292  0.437
1990 Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PJ, Tischfield JA, Zöllner N. Identification of a splice mutation at the adenine phosphoribosyltransferase locus in a German family. Klinische Wochenschrift. 69: 1152-5. PMID 2135300 DOI: 10.1007/BF01815434  0.521
1990 Sahota A, Chen J, Asaki K, Takeuchi H, Stambrook PJ, Tischfield JA. Identification of a common nonsense mutation in Japanese patients with type I adenine phosphoribosyltransferase deficiency. Nucleic Acids Research. 18: 5915-6. PMID 1977137 DOI: 10.1093/nar/18.19.5915  0.495
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