93 related articles for article (PubMed ID: 9693033)
41. Isolation and characterization of the human UGT2B15 gene, localized within a cluster of UGT2B genes and pseudogenes on chromosome 4.
Turgeon D; Carrier JS; Lévesque E; Beatty BG; Bélanger A; Hum DW
J Mol Biol; 2000 Jan; 295(3):489-504. PubMed ID: 10623541
[TBL] [Abstract][Full Text] [Related]
42. Identification of a novel protocadherin gene (PCDH11) on the human XY homology region in Xq21.3.
Yoshida K; Sugano S
Genomics; 1999 Dec; 62(3):540-3. PubMed ID: 10644456
[TBL] [Abstract][Full Text] [Related]
43. Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel.
Sossey-Alaoui K; Lyon JA; Jones L; Abidi FE; Hartung AJ; Hane B; Schwartz CE; Stevenson RE; Srivastava AK
Genomics; 1999 Sep; 60(3):330-40. PubMed ID: 10493832
[TBL] [Abstract][Full Text] [Related]
44. Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24.
Mansour SJ; Herbrick JA; Scherer SW; Melançon P
Genomics; 1998 Dec; 54(2):323-7. PubMed ID: 9828135
[TBL] [Abstract][Full Text] [Related]
45. The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.
Lerman MI; Minna JD
Cancer Res; 2000 Nov; 60(21):6116-33. PubMed ID: 11085536
[TBL] [Abstract][Full Text] [Related]
46. Identification and characterization of ASXL3 gene in silico.
Katoh M; Katoh M
Int J Oncol; 2004 Jun; 24(6):1617-22. PubMed ID: 15138607
[TBL] [Abstract][Full Text] [Related]
47. Identification of SATB2 as the cleft palate gene on 2q32-q33.
FitzPatrick DR; Carr IM; McLaren L; Leek JP; Wightman P; Williamson K; Gautier P; McGill N; Hayward C; Firth H; Markham AF; Fantes JA; Bonthron DT
Hum Mol Genet; 2003 Oct; 12(19):2491-501. PubMed ID: 12915443
[TBL] [Abstract][Full Text] [Related]
48. TRIM45, a novel human RBCC/TRIM protein, inhibits transcriptional activities of ElK-1 and AP-1.
Wang Y; Li Y; Qi X; Yuan W; Ai J; Zhu C; Cao L; Yang H; Liu F; Wu X; Liu M
Biochem Biophys Res Commun; 2004 Oct; 323(1):9-16. PubMed ID: 15351693
[TBL] [Abstract][Full Text] [Related]
49. X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.
Pawar H; Bingham EL; Hiriyanna K; Segal M; Richards JE; Sieving PA
Hum Hered; 1996; 46(6):329-35. PubMed ID: 8956029
[TBL] [Abstract][Full Text] [Related]
50. Transcription mapping in a 700-kb region around the DXS52 locus in Xq28: isolation of six novel transcripts and a novel ATPase isoform (hPMCA5).
Heiss NS; Rogner UC; Kioschis P; Korn B; Poustka A
Genome Res; 1996 Jun; 6(6):478-91. PubMed ID: 8828037
[TBL] [Abstract][Full Text] [Related]
51. Construction of a 3-Mb contig and partial transcript map of the central region of mouse chromosome 11.
Watkins-Chow DE; Douglas KR; Buckwalter MS; Probst FJ; Camper SA
Genomics; 1997 Oct; 45(1):147-57. PubMed ID: 9339371
[TBL] [Abstract][Full Text] [Related]
52. Positional cloning of the gene associated with X-linked juvenile retinoschisis.
Sauer CG; Gehrig A; Warneke-Wittstock R; Marquardt A; Ewing CC; Gibson A; Lorenz B; Jurklies B; Weber BH
Nat Genet; 1997 Oct; 17(2):164-70. PubMed ID: 9326935
[TBL] [Abstract][Full Text] [Related]
53. A streamlined random sequencing strategy for finding coding exons.
Claverie JM
Genomics; 1994 Oct; 23(3):575-81. PubMed ID: 7851885
[TBL] [Abstract][Full Text] [Related]
54. An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.
Van de Vosse E; Bergen AA; Meershoek EJ; Oosterwijk JC; Gregory S; Bakker B; Weissenbach J; Coffey AJ; van Ommen GJ; Den Dunnen JT
Eur J Hum Genet; 1996; 4(2):101-4. PubMed ID: 8744027
[TBL] [Abstract][Full Text] [Related]
55. Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region.
Montini E; Andolfi G; Caruso A; Buchner G; Walpole SM; Mariani M; Consalez G; Trump D; Ballabio A; Franco B
Genomics; 1998 Aug; 51(3):427-33. PubMed ID: 9721213
[TBL] [Abstract][Full Text] [Related]
56. Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: further narrowing of the RS candidate region.
Dumur V; Trivier E; Puech B; Peugnet F; Zanlonghi X; Hache JC; Hanauer A
Hum Genet; 1995 Jul; 96(1):79-82. PubMed ID: 7607659
[TBL] [Abstract][Full Text] [Related]
57. Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains.
de Conciliis L; Marchitiello A; Wapenaar MC; Borsani G; Giglio S; Mariani M; Consalez GG; Zuffardi O; Franco B; Ballabio A; Banfi S
Genomics; 1998 Jul; 51(2):243-50. PubMed ID: 9722947
[TBL] [Abstract][Full Text] [Related]
58. The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability.
Klink A; Schiebel K; Winkelmann M; Rao E; Horsthemke B; Lüdecke HJ; Claussen U; Scherer G; Rappold G
Hum Mol Genet; 1995 May; 4(5):869-78. PubMed ID: 7633447
[TBL] [Abstract][Full Text] [Related]
59. Tentative mapping of transcription-induced interchromosomal interaction using chimeric EST and mRNA data.
Unneberg P; Claverie JM
PLoS One; 2007 Feb; 2(2):e254. PubMed ID: 17330142
[TBL] [Abstract][Full Text] [Related]
60. Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS).
Schaefer L; Ballabio A; Zoghbi HY
Genomics; 1996 Jun; 34(2):166-72. PubMed ID: 8661044
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
