829 related articles for article (PubMed ID: 8964845)
1. Genomic structure of a Y-specific ribonucleic acid binding motif-containing gene: a putative candidate for a subset of male infertility.
Najmabadi H; Chai N; Kapali A; Subbarao MN; Bhasin D; Woodhouse E; Yen P; Bhasin S
J Clin Endocrinol Metab; 1996 Jun; 81(6):2159-64. PubMed ID: 8964845
[TBL] [Abstract][Full Text] [Related]
2. Degeneracy in human multicopy RBM (YRRM), a candidate spermatogenesis gene.
Prosser J; Inglis JD; Condie A; Ma K; Kerr S; Thakrar R; Taylor K; Cameron JM; Cooke HJ
Mamm Genome; 1996 Nov; 7(11):835-42. PubMed ID: 8875892
[TBL] [Abstract][Full Text] [Related]
3. Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome.
Chai NN; Salido EC; Yen PH
Genomics; 1997 Oct; 45(2):355-61. PubMed ID: 9344660
[TBL] [Abstract][Full Text] [Related]
4. Molecular isolation and characterization of an expressed gene from the human Y chromosome.
Zhang JS; Yang-Feng TL; Muller U; Mohandas TK; de Jong PJ; Lau YF
Hum Mol Genet; 1992 Dec; 1(9):717-26. PubMed ID: 1284595
[TBL] [Abstract][Full Text] [Related]
5. Structure of the murine fifth complement component (C5) gene. A large, highly interrupted gene with a variant donor splice site and organizational homology with the third and fourth complement component genes.
Haviland DL; Haviland JC; Fleischer DT; Wetsel RA
J Biol Chem; 1991 Jun; 266(18):11818-25. PubMed ID: 1711041
[TBL] [Abstract][Full Text] [Related]
6. Structural organization and complete sequence of the human alpha-N-acetylgalactosaminidase gene: homology with the alpha-galactosidase A gene provides evidence for evolution from a common ancestral gene.
Wang AM; Desnick RJ
Genomics; 1991 May; 10(1):133-42. PubMed ID: 1646157
[TBL] [Abstract][Full Text] [Related]
7. An exon map of the AZFc male infertility region of the human Y chromosome.
Wong J; Blanco P; Affara NA
Mamm Genome; 1999 Jan; 10(1):57-61. PubMed ID: 9892735
[TBL] [Abstract][Full Text] [Related]
8. Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy.
Najmabadi H; Huang V; Yen P; Subbarao MN; Bhasin D; Banaag L; Naseeruddin S; de Kretser DM; Baker HW; McLachlan RI
J Clin Endocrinol Metab; 1996 Apr; 81(4):1347-52. PubMed ID: 8636331
[TBL] [Abstract][Full Text] [Related]
9. Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism.
Szumlanski C; Otterness D; Her C; Lee D; Brandriff B; Kelsell D; Spurr N; Lennard L; Wieben E; Weinshilboum R
DNA Cell Biol; 1996 Jan; 15(1):17-30. PubMed ID: 8561894
[TBL] [Abstract][Full Text] [Related]
10. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
11. Cloning and functional expression of the luteinizing hormone receptor complementary deoxyribonucleic acid from the marmoset monkey testis: absence of sequences encoding exon 10 in other species.
Zhang FP; Rannikko AS; Manna PR; Fraser HM; Huhtaniemi IT
Endocrinology; 1997 Jun; 138(6):2481-90. PubMed ID: 9165039
[TBL] [Abstract][Full Text] [Related]
12. The mouse lens fiber-cell intrinsic membrane protein MP19 gene (Lim2) and granule membrane protein GMP-17 gene (Nkg7): Isolation and sequence analysis of two neighboring genes.
Zhou L; Li X; Church RL
Mol Vis; 2001 Apr; 7():79-88. PubMed ID: 11290961
[TBL] [Abstract][Full Text] [Related]
13. A putative human male infertility gene DAZLA: genomic structure and methylation status.
Chai NN; Phillips A; Fernandez A; Yen PH
Mol Hum Reprod; 1997 Aug; 3(8):705-8. PubMed ID: 9294855
[TBL] [Abstract][Full Text] [Related]
14. Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene.
Chatterjee TK; Eapen A; Kanis AB; Fisher RA
Genomics; 1997 Oct; 45(2):429-33. PubMed ID: 9344672
[TBL] [Abstract][Full Text] [Related]
15. Association of a single-nucleotide polymorphism of the deleted-in-azoospermia-like gene with susceptibility to spermatogenic failure.
Teng YN; Lin YM; Lin YH; Tsao SY; Hsu CC; Lin SJ; Tsai WC; Kuo PL
J Clin Endocrinol Metab; 2002 Nov; 87(11):5258-64. PubMed ID: 12414900
[TBL] [Abstract][Full Text] [Related]
16. Structure and expression of the human lysyl hydroxylase gene (PLOD): introns 9 and 16 contain Alu sequences at the sites of recombination in Ehlers-Danlos syndrome type VI patients.
Heikkinen J; Hautala T; Kivirikko KI; Myllylä R
Genomics; 1994 Dec; 24(3):464-71. PubMed ID: 7713497
[TBL] [Abstract][Full Text] [Related]
17. Genomic sequence of the DAX1 gene: an orphan nuclear receptor responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
Guo W; Burris TP; Zhang YH; Huang BL; Mason J; Copeland KC; Kupfer SR; Pagon RA; McCabe ER
J Clin Endocrinol Metab; 1996 Jul; 81(7):2481-6. PubMed ID: 8675564
[TBL] [Abstract][Full Text] [Related]
18. The gene for human protein Z is localized to chromosome 13 at band q34 and is coded by eight regular exons and one alternative exon.
Fujimaki K; Yamazaki T; Taniwaki M; Ichinose A
Biochemistry; 1998 May; 37(19):6838-46. PubMed ID: 9578570
[TBL] [Abstract][Full Text] [Related]
19. Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum.
Pulkkinen L; Nakano A; Ringpfeil F; Uitto J
Hum Genet; 2001 Sep; 109(3):356-65. PubMed ID: 11702217
[TBL] [Abstract][Full Text] [Related]
20. Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
Hansen JJ; Bross P; Westergaard M; Nielsen MN; Eiberg H; Børglum AD; Mogensen J; Kristiansen K; Bolund L; Gregersen N
Hum Genet; 2003 Jan; 112(1):71-7. PubMed ID: 12483302
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
