| Year |
Citation |
Score |
| 2009 |
Beuten J, Garcia D, Brand TC, He X, Balic I, Canby-Hagino E, Troyer DA, Baillargeon J, Hernandez J, Thompson IM, Leach RJ, Naylor SL. Semaphorin 3B and 3F single nucleotide polymorphisms are associated with prostate cancer risk and poor prognosis. The Journal of Urology. 182: 1614-20. PMID 19683737 DOI: 10.1016/J.Juro.2009.06.016 |
0.397 |
|
| 2009 |
Park JS, Sharma LK, Li H, Xiang R, Holstein D, Wu J, Lechleiter J, Naylor SL, Deng JJ, Lu J, Bai Y. A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis. Human Molecular Genetics. 18: 1578-89. PMID 19208652 DOI: 10.1093/Hmg/Ddp069 |
0.3 |
|
| 2007 |
Naylor SL. SNPs associated with prostate cancer risk and prognosis. Frontiers in Bioscience : a Journal and Virtual Library. 12: 4111-31. PMID 17485362 DOI: 10.2741/2375 |
0.402 |
|
| 2006 |
Muzny DM, Scherer SE, Kaul R, Wang J, Yu J, Sudbrak R, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, Gill R, Gunaratne P, Harris RA, Hawes AC, ... ... Naylor SL, et al. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 440: 1194-8. PMID 16641997 DOI: 10.1038/Nature04728 |
0.491 |
|
| 2006 |
Vijayakumar S, Hall DC, Reveles XT, Troyer DA, Thompson IM, Garcia D, Xiang R, Leach RJ, Johnson-Pais TL, Naylor SL. Detection of recurrent copy number loss at Yp11.2 involving TSPY gene cluster in prostate cancer using array-based comparative genomic hybridization. Cancer Research. 66: 4055-64. PMID 16618725 DOI: 10.1158/0008-5472.Can-05-3822 |
0.721 |
|
| 2006 |
Canby-Hagino ED, Garda D, Thompson lM, Troyer D, Baillargeon J, Brand TC, Leach R, Naylor SL. 821: The VEGF+405 CC Polymorphism is Associated with Prostate Cancers of Poor Prognosis The Journal of Urology. 175: 265-265. DOI: 10.1016/S0022-5347(18)33057-X |
0.372 |
|
| 2006 |
Brand TC, Garcia D, Canby-Hagino E, Thompson IM, Troyer D, Baillargeon J, Leach R, Naylor SL. 242: Variants of Semaphorin 3F are Associated with Prostate Cancer Prognosis The Journal of Urology. 175: 80-80. DOI: 10.1016/S0022-5347(18)32509-6 |
0.346 |
|
| 2005 |
Vijayakumar S, Garcia D, Hensel CH, Banerjee M, Bracht T, Xiang R, Kagan J, Naylor SL. The human Y chromosome suppresses the tumorigenicity of PC-3, a human prostate cancer cell line, in athymic nude mice. Genes, Chromosomes & Cancer. 44: 365-72. PMID 16080199 DOI: 10.1002/Gcc.20250 |
0.737 |
|
| 2005 |
Naylor SL, He X, Xiang R, Garcia DK, Canby-Hagino ED, Baillargeon J, Hernandez J, Troyer DA, Thompson IM, Leach RJ. 1414: Aggressive Prostate Cancer is Associated with Nucleotide Variants of the Semaphorin 3F Gene The Journal of Urology. 173: 383-383. DOI: 10.1016/S0022-5347(18)35548-4 |
0.398 |
|
| 2004 |
Troyer DA, Mubiru J, Leach RJ, Naylor SL. Promise and challenge: Markers of prostate cancer detection, diagnosis and prognosis. Disease Markers. 20: 117-128. PMID 15322319 DOI: 10.1155/2004/509276 |
0.39 |
|
| 2004 |
Thompson IM, Leach R, Troyer D, Pollock B, Naylor S, Higgins B. Relationship of body mass index and prostate specific antigen in a population-based study Urologic Oncology: Seminars and Original Investigations. 22: 127-131. PMID 15082010 DOI: 10.1016/S1078-1439(03)00171-6 |
0.324 |
|
| 2003 |
Thompson I, Leach RJ, Pollock BH, Naylor SL. Prostate cancer and prostate-specific antigen: the more we know, the less we understand. Journal of the National Cancer Institute. 95: 1027-8. PMID 12865440 DOI: 10.1093/Jnci/95.14.1027 |
0.355 |
|
| 2003 |
Leach R, Pollock B, Basler J, Troyer D, Naylor S, Thompson IM. Chemoprevention of prostate cancer: Focus on key opportunities and clinical trials Urologic Clinics of North America. 30: 227-237. PMID 12735500 DOI: 10.1016/S0094-0143(02)00178-7 |
0.347 |
|
| 2002 |
Xiang R, Davalos AR, Hensel CH, Zhou XJ, Tse C, Naylor SL. Semaphorin 3F gene from human 3p21.3 suppresses tumor formation in nude mice. Cancer Research. 62: 2637-43. PMID 11980661 |
0.326 |
|
| 2002 |
Tse C, Xiang RH, Bracht T, Naylor SL. Human Semaphorin 3B (SEMA3B) located at chromosome 3p21.3 suppresses tumor formation in an adenocarcinoma cell line. Cancer Research. 62: 542-6. PMID 11809707 |
0.334 |
|
| 2001 |
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, ... ... Naylor SL, et al. Initial sequencing and analysis of the human genome. Nature. 409: 860-921. PMID 11237011 DOI: 10.1038/35057062 |
0.316 |
|
| 2001 |
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, Fitzhugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, ... ... Naylor SL, et al. Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) Nature. 412: 565-566. DOI: 10.1038/35087627 |
0.305 |
|
| 2000 |
Hejna JA, Timmers CD, Reifsteck C, Bruun DA, Lucas LW, Jakobs PM, Toth-Fejel S, Unsworth N, Clemens SL, Garcia DK, Naylor SL, Thayer MJ, Olson SB, Grompe M, Moses RE. Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3. American Journal of Human Genetics. 66: 1540-51. PMID 10762542 DOI: 10.1086/302896 |
0.544 |
|
| 1999 |
Riazi MA, Brinkman-Mills P, Johnson A, Naylor SL, Minoshima S, Shimizu N, Baldini A, McDermid HE. Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2. Genomics. 62: 90-4. PMID 10585773 DOI: 10.1006/Geno.1999.5975 |
0.416 |
|
| 1998 |
Taskén K, Naylor SL, Solberg R, Jahnsen T. Mapping of the Gene Encoding the Regulatory Subunit RIIα of cAMP-Dependent Protein Kinase (Locus PRKAR2A) to Human Chromosome Region 3p21.3–p21.2 Genomics. 50: 378-381. PMID 9676433 DOI: 10.1006/Geno.1998.5326 |
0.522 |
|
| 1998 |
VanDenBrink AM, Vergouwe MN, Ophoff RA, Naylor SL, Dauwerse HG, Saxena PR, Ferrari MD, Frants RR. Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients. American Journal of Medical Genetics. 77: 415-420. PMID 9632173 DOI: 10.1002/(Sici)1096-8628(19980605)77:5<415::Aid-Ajmg12>3.0.Co;2-L |
0.389 |
|
| 1998 |
Hardiman G, Jenkins NA, Copeland NG, Gilbert DJ, Garcia DK, Naylor SL, Kastelein RA, Bazan JF. Genetic structure and chromosomal mapping of MyD88. Genomics. 45: 332-9. PMID 9344657 DOI: 10.1006/Geno.1997.4940 |
0.485 |
|
| 1997 |
Kok K, Naylor SL, Buys CHCM. Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes Advances in Cancer Research. 71: 27-92. PMID 9111863 DOI: 10.1016/S0065-230X(08)60096-2 |
0.414 |
|
| 1997 |
Moghrabi NN, Naylor SL, Veldhoven PPV, Baumgart E, Dawson DB, Bennett MJ. Assignment of the Human Peroxisomal Branched-Chain Acyl-CoA Oxidase Gene to Chromosome 3p21·1-p14·2 by Rodent/Human Somatic Cell Hybridization Biochemical and Biophysical Research Communications. 231: 767-769. PMID 9070889 DOI: 10.1006/Bbrc.1997.6192 |
0.528 |
|
| 1996 |
Polymeropoulos MH, Ide SE, Becker K, Naylor SL. Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22. Cancer Genetics and Cytogenetics. 92: 46-9. PMID 8956871 DOI: 10.1016/S0165-4608(96)00148-3 |
0.44 |
|
| 1996 |
Xiang RH, Hensel CH, Garcia DK, Carlson HC, Kok K, Daly MC, Kerbacher K, van den Berg A, Veldhuis P, Buys CH, Naylor SL. Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancer. Genomics. 32: 39-48. PMID 8786119 DOI: 10.1006/Geno.1996.0074 |
0.488 |
|
| 1996 |
Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, ... ... Naylor S, et al. Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996. Cytogenetics and Cell Genetics. 73: 255-73. PMID 8751373 DOI: 10.1159/000134352 |
0.464 |
|
| 1996 |
Draaijers TG, Berg Avd, Kokl K, Timmer T, Veen AYvd, Veldhuis PMJF, Naylor SL, Smith DI, Buys CHCM. A homozygous deletion at FRA3B in a lung adenocarcinoma cell line with normal expression of the FHIT gene Cancer Genetics and Cytogenetics. 91: 170. DOI: 10.1016/S0165-4608(97)82644-1 |
0.328 |
|
| 1995 |
Naylor SL, Daly MC, Xiang RH, Hensel CH, Kok K, Carlson H, Killary AM, Drabkin H, Buys C. Chromosome 3 and the isolation of a tumor suppressor gene Cancer Genetics and Cytogenetics. 84: 130. DOI: 10.1016/0165-4608(96)85215-0 |
0.485 |
|
| 1994 |
Legerski RJ, Liu P, Li L, Peterson CA, Zhao Y, Leach RJ, Naylor SL, Siciliano MJ. Assignment of xeroderma pigmentosum group C (XPC) gene to chromosome 3p25. Genomics. 21: 266-9. PMID 8088800 DOI: 10.1006/Geno.1994.1256 |
0.552 |
|
| 1994 |
O'Connell P, Leach RJ, Rains D, Taylor T, Garcia D, Ballard L, Holik P, Weissenbach J, Sherman S, Wilkie P, Weber JL, Naylor SL. A PCR-Based Genetic Map for Human Chromosome 3 Genomics. 24: 557-567. PMID 7713508 DOI: 10.1006/Geno.1994.1666 |
0.43 |
|
| 1994 |
Veldhuis PMJF, Kok K, Veen AYvd, Berg Avd, Schoenmakers E, Ven Wvd, Daly MC, Naylor SL, Buys CHCM. A long range map covering a homozygously deleted region in a small cell lung cancer (SCLC) derived cell line Cancer Genetics and Cytogenetics. 77: 188. DOI: 10.1016/0165-4608(94)90387-5 |
0.341 |
|
| 1994 |
Kok K, Berg Avd, Veldhuis PMJF, Hulsbeek M, Veen AYvd, Naylor SL, Buys CHCM. Characterisation of genes mapping in a region of 3p21 homozygously deleted in a small cell lung cancer (SCLC) derived cell line Cancer Genetics and Cytogenetics. 77: 187. DOI: 10.1016/0165-4608(94)90386-7 |
0.391 |
|
| 1993 |
Todd S, Naylor SL. Dinucleotide repeat polymorphisms at the D2S108 and D2S109 loci Human Molecular Genetics. 2: 490-490. PMID 8504316 DOI: 10.1093/Hmg/2.4.490-A |
0.34 |
|
| 1993 |
Dubois BL, Naylor SL. Characterization of NIGMS Human/Rodent Somatic Cell Hybrid Mapping Panel 2 by PCR Genomics. 16: 315-319. PMID 8314569 DOI: 10.1006/Geno.1993.1191 |
0.525 |
|
| 1993 |
Todd S, Sherman SL, Naylor SL. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map. Genomics. 16: 612-618. PMID 8100800 DOI: 10.1006/Geno.1993.1238 |
0.449 |
|
| 1992 |
Todd S, Naylor SL. New chromosomal mapping assignments for argininosuccinate synthetase pseudogene 1, interferon-β3 gene, and the diazepam binding inhibitor gene Somatic Cell and Molecular Genetics. 18: 381-385. PMID 1440058 DOI: 10.1007/Bf01235761 |
0.55 |
|
| 1992 |
Rajput B, Ma J, Muniappa N, Schantz L, Naylor SL, Lalley PA, Vijay IK. Mouse UDP-GlcNAc: dolichyl-phosphate N-acetylglucosaminephosphotransferase. Molecular cloning of the cDNA, generation of anti-peptide antibodies and chromosomal localization. Biochemical Journal. 285: 985-992. PMID 1323278 DOI: 10.1042/Bj2850985 |
0.408 |
|
| 1991 |
Theune S, Fung J, Todd S, Sakaguchi AY, Naylor SL. PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids. Genomics. 9: 511-516. PMID 2032722 DOI: 10.1016/0888-7543(91)90418-E |
0.533 |
|
| 1991 |
Naylor SL. Workshop on human chromosome 3. Genomics. 9: 213-214. PMID 2004765 DOI: 10.1016/0888-7543(91)90243-8 |
0.513 |
|
| 1991 |
Han E, Moyer MP, Naylor S, Sakaguchi AY. Mutation in the TP53 gene in colorectal carcinoma detected by polymerase chain reaction. Genes, Chromosomes and Cancer. 3: 313-317. PMID 1958596 DOI: 10.1002/Gcc.2870030411 |
0.377 |
|
| 1991 |
Todd S, Naylor SL. Dinucleotide repeat polymorphism in the human tubulin alpha 1 (testis specific) gene (TUBA1) Nucleic Acids Research. 19: 3755-3755. PMID 1852622 DOI: 10.1093/Nar/19.13.3755 |
0.365 |
|
| 1991 |
Smith EA, Seldin MF, Martinez L, Watson ML, Choudhury GG, Lalley PA, Pierce J, Aaronson S, Barker J, Naylor SL. Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5. Proceedings of the National Academy of Sciences of the United States of America. 88: 4811-5. PMID 1647018 DOI: 10.1073/Pnas.88.11.4811 |
0.435 |
|
| 1991 |
Todd S, Naylor SL. Dinucleotide repeat polymorphism in the human surfactant-associated protein 3 gene (SFTP3). Nucleic Acids Research. 19: 3756-3756. DOI: 10.1093/Nar/19.13.3756-A |
0.373 |
|
| 1991 |
Todd S, Naylor SL. Dinucleotide repeat polymorphism in the human interleukin 1, alpha gene (IL1A) Nucleic Acids Research. 19: 3756-3756. DOI: 10.1093/Nar/19.13.3756 |
0.354 |
|
| 1990 |
Sakaguchi AY, Lalley PA, Choudhury GG, Martinez L, Han ES, Killary AM, Naylor SL, Wang LM. Mouse melanoma growth stimulatory activity gene (Mgsa) is polymorphic and syntenic with the W, patch, rumpwhite, and recessive spotting loci on chromosome 5. Genomics. 5: 629-32. PMID 2575589 DOI: 10.1016/0888-7543(89)90033-5 |
0.5 |
|
| 1989 |
Hsieh CL, Lee WH, Lee EY, Killary AM, Lalley PA, Naylor SL. Assignment of retinoblastoma susceptibility gene to mouse chromosome 14. Somatic Cell and Molecular Genetics. 15: 461-4. PMID 2781416 DOI: 10.1007/Bf01534896 |
0.563 |
|
| 1989 |
Todd S, McGill JR, McCombs JL, Moore CM, Weider I, Naylor SL. cDNA sequence, interspecies comparison, and gene mapping analysis of argininosuccinate lyase. Genomics. 4: 53-9. PMID 2644168 DOI: 10.1016/0888-7543(89)90314-5 |
0.549 |
|
| 1989 |
Johnson BE, Whang-peng J, Naylor SL, Zbar B, Brauch H, Lee E, Simmons A, Russell E, Nam MH, Gazdar AF. Retention of Chromosome 3 in Extrapulmonary Small Cell Cancer Shown by Molecular and Cytogenetic Studies Journal of the National Cancer Institute. 81: 1223-1228. PMID 2569043 DOI: 10.1093/Jnci/81.16.1223 |
0.477 |
|
| 1989 |
Naylor SL, Marshall A, Hensel C, Martinez PF, Holley B, Sakaguchi AY. The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer Genomics. 4: 355-361. PMID 2565880 DOI: 10.1016/0888-7543(89)90342-X |
0.448 |
|
| 1989 |
Fujimoto M, Fults DW, Thomas GA, Nakamura Y, Heilbrun MP, White R, Story JL, Naylor SL, Kagan-Hallet KS, Sheridan PJ. Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme. Genomics. 4: 210-4. PMID 2544511 DOI: 10.1016/0888-7543(89)90302-9 |
0.496 |
|
| 1989 |
McGuire SE, Fuqua SAW, Naylor SL, Helin-Davis DA, McGuire WL. Chromosomal assignments of human 27-kDa heat shock protein gene family Somatic Cell and Molecular Genetics. 15: 167-171. PMID 2538929 DOI: 10.1007/Bf01535078 |
0.375 |
|
| 1989 |
Naylor SL, Helin-Davies D, Charoenworawat P, Vaillarreal XC, Long GL. The human osteonectin gene (OSN) has TaqI and MspI polymorphisms. Nucleic Acids Research. 17: 6753. PMID 2476719 DOI: 10.1093/Nar/17.16.6753 |
0.393 |
|
| 1988 |
Long GL, Marshall A, Gardner JC, Naylor SL. Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectively. Somatic Cell and Molecular Genetics. 14: 93-8. PMID 2829367 DOI: 10.1007/Bf01535052 |
0.513 |
|
| 1988 |
Naylor SL, Marshall A, Johnson BE, Minna JD, Gazdar AF, Whang-Peng J, Lee EC, Sakaguchi AY. Chromosome 3P in small cell lung cancer Lung Cancer. 4: 117-120. DOI: 10.1016/S0169-5002(88)80033-3 |
0.524 |
|
| 1987 |
Teng CT, Pentecost BT, Marshall A, Solomon A, Bowman BH, Lalley PA, Naylor SL. Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9 Somatic Cell and Molecular Genetics. 13: 689-693. PMID 3478818 DOI: 10.1007/Bf01534490 |
0.567 |
|
| 1987 |
Naylor SL, Altruda F, Marshall A, Silengo L, Bowman BH. Hemopexin is localized to human chromosome 11 Somatic Cell and Molecular Genetics. 13: 355-358. PMID 3455011 DOI: 10.1007/Bf01534930 |
0.511 |
|
| 1987 |
Naylor SL, McGill JR, Zabel BU. [21] In situ hybridization of metaphase and prometaphase chromosomes Methods in Enzymology. 151: 279-292. PMID 3431444 DOI: 10.1016/S0076-6879(87)51024-2 |
0.525 |
|
| 1987 |
Higuchi K, Monge JC, Lee N, Law SW, Brewer HB, Sakaguchi AY, Naylor SL. The human apoB-100 gene: apoB-100 is encoded by a single copy gene in the human genome. Biochemical and Biophysical Research Communications. 144: 1332-9. PMID 3034278 DOI: 10.1016/0006-291X(87)91456-2 |
0.412 |
|
| 1987 |
Rotwein P, Naylor SL, Chirgwin JM. Human insulin-related DNA sequences map to chromosomes 2 and 11. Somatic Cell and Molecular Genetics. 12: 625-31. PMID 3024335 DOI: 10.1007/Bf01671947 |
0.436 |
|
| 1987 |
Rajput B, Marshall A, Killary AM, Lalley PA, Naylor SL, Belin D, Rickles RJ, Strickland S. Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse. Somatic Cell and Molecular Genetics. 13: 581-6. PMID 2821634 DOI: 10.1007/Bf01534500 |
0.511 |
|
| 1986 |
Naylor SL, Sakaguchi AY, McDonald L, Todd S, Lalley PA, Shows TB, Chin WW. Mapping thyrotropin β subunit gene in man and mouse Somatic Cell and Molecular Genetics. 12: 307-311. PMID 3459258 DOI: 10.1007/Bf01570791 |
0.521 |
|
| 1985 |
Todd S, Yoshida MC, Fang XE, McDonald L, Jacobs J, Heinrich G, Bell GI, Naylor SL, Sakaguchi AY. Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1. Biochemical and Biophysical Research Communications. 131: 1175-1180. PMID 3902019 DOI: 10.1016/0006-291X(85)90214-1 |
0.388 |
|
| 1985 |
Law SW, Lee N, Monge JC, Brewer HB, Sakaguchi AY, Naylor SL. Human ApoB-100 gene resides in the p23----pter region of chromosome 2. Biochemical and Biophysical Research Communications. 131: 1003-12. PMID 3840371 DOI: 10.1016/0006-291X(85)91339-7 |
0.51 |
|
| 1985 |
Nedwin GE, Jarrett-Nedwin J, Smith DH, Naylor SL, Sakaguchi AY, Goeddel DV, Gray PW. Structure and chromosomal localization of the human lymphotoxin gene Journal of Cellular Biochemistry. 29: 171-181. PMID 3001109 DOI: 10.1002/Jcb.240290302 |
0.507 |
|
| 1985 |
Sakaguchi AY, Mohandas T, Naylor SL. A human c-src gene resides on the proximal long arm of chromosome 20 (cen→q131) Cancer Genetics and Cytogenetics. 18: 123-129. PMID 2996754 DOI: 10.1016/0165-4608(85)90062-7 |
0.477 |
|
| 1985 |
Nedwin GE, Naylor SL, Sakaguchi AY, Smith D, Jarrett-Nedwin J, Pennica D, Goeddel DV, Gray PW. Human lymphotoxin and tumor necrosis factor genes: Structure, homology and chromosomal localization Nucleic Acids Research. 13: 6361-6373. PMID 2995927 DOI: 10.1093/Nar/13.17.6361 |
0.497 |
|
| 1985 |
Wallace MR, Naylor SL, Kluve-Beckerman B, Long GL, McDonald L, Shows TB, Benson MD. Localization of the human prealbumin gene to chromosome 18. Biochemical and Biophysical Research Communications. 129: 753-8. PMID 2990465 DOI: 10.1016/0006-291X(85)91956-4 |
0.51 |
|
| 1985 |
Yang F, Brune JL, Naylor SL, Cupples RL, Naberhaus KH, Bowman BH. Human group-specific component (Gc) is a member of the albumin family Proceedings of the National Academy of Sciences of the United States of America. 82: 7994-7998. PMID 2415977 DOI: 10.1073/Pnas.82.23.7994 |
0.462 |
|
| 1985 |
McGILL JR, Naylor SL, Yang F, Bowman BH. Isolation and Characterization of Hp10: a Specific Human Hepatic Protein cDNA Protides of the Biological Fluids. 33: 245-248. DOI: 10.1016/B978-0-08-033215-4.50060-1 |
0.458 |
|
| 1985 |
Naylor SL, Sakaguchi AY. Chromosome Mapping of Serum Protein Genes Protides of the Biological Fluids. 33: 71-76. DOI: 10.1016/B978-0-08-033215-4.50020-0 |
0.558 |
|
| 1985 |
Bowman BH, Yang F, Brune JL, Naylor SL, Barnett DR, McGILL JR, Moore CM, Lum JB, McCOMBS J. Organization and Chromosomal Locations of Genes Encoding Human Plasma Proteins Protides of the Biological Fluids. 33: 15-20. DOI: 10.1016/B978-0-08-033215-4.50007-8 |
0.411 |
|
| 1984 |
Yang F, Lum JB, McGill JR, Moore CM, Naylor SL, Bragt PHv, Baldwin WD, Bowman BH. Human transferrin: cDNA characterization and chromosomal localization Proceedings of the National Academy of Sciences of the United States of America. 81: 2752-2756. PMID 6585826 DOI: 10.1073/Pnas.81.9.2752 |
0.533 |
|
| 1984 |
Chirgwin JM, Schaefer IM, Rotwein PS, Piccini N, Gross KW, Naylor SL. Human renin gene is on chromosome 1. Somatic Cell and Molecular Genetics. 10: 415-21. PMID 6379904 DOI: 10.1007/Bf01535637 |
0.531 |
|
| 1982 |
Shows TB, Sakaguchi AY, Naylor SL. Mapping the Human Genome, Cloned Genes, DNA Polymorphisms, and Inherited Disease Advances in Human Genetics. 12: 341-452. PMID 6957143 DOI: 10.1007/978-1-4615-8315-8_5 |
0.455 |
|
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