These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
87 related articles for article (PubMed ID: 9266672)
1. The 239AB gene on chromosome 22: a novel member of an ancient gene family. Schwartz F; Ota T Gene; 1997 Jul; 194(1):57-62. PubMed ID: 9266672 [TBL] [Abstract][Full Text] [Related]
2. cDNA sequence, genomic organization, and evolutionary conservation of a novel gene from the WAGR region. Schwartz F; Eisenman R; Knoll J; Gessler M; Bruns G Genomics; 1995 Sep; 29(2):526-32. PubMed ID: 8666403 [TBL] [Abstract][Full Text] [Related]
3. Characterization of an evolutionarily conserved metallophosphoesterase that is expressed in the fetal brain and associated with the WAGR syndrome. Tyagi R; Shenoy AR; Visweswariah SS J Biol Chem; 2009 Feb; 284(8):5217-28. PubMed ID: 19004815 [TBL] [Abstract][Full Text] [Related]
4. A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome. Rosier MF; Goguel AF; Martin A; Le Paslier D; Couillin P; Houlgatte R; Bernheim A; Auffray C; Devignes MD Genomics; 1994 Nov; 24(1):69-77. PubMed ID: 7896291 [TBL] [Abstract][Full Text] [Related]
5. Human brain factor 1, a new member of the fork head gene family. Murphy DB; Wiese S; Burfeind P; Schmundt D; Mattei MG; Schulz-Schaeffer W; Thies U Genomics; 1994 Jun; 21(3):551-7. PubMed ID: 7959731 [TBL] [Abstract][Full Text] [Related]
6. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes. Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227 [TBL] [Abstract][Full Text] [Related]
7. Cloning, functional study and comparative mapping of Luzp2 to mouse chromosome 7 and human chromosome 11p13-11p14. Wu M; Michaud EJ; Johnson DK Mamm Genome; 2003 May; 14(5):323-34. PubMed ID: 12856284 [TBL] [Abstract][Full Text] [Related]
8. LGR4/GPR48 inactivation leads to aniridia-genitourinary anomalies-mental retardation syndrome defects. Yi T; Weng J; Siwko S; Luo J; Li D; Liu M J Biol Chem; 2014 Mar; 289(13):8767-80. PubMed ID: 24519938 [TBL] [Abstract][Full Text] [Related]
9. A novel transcription factor, ELF5, belongs to the ELF subfamily of ETS genes and maps to human chromosome 11p13-15, a region subject to LOH and rearrangement in human carcinoma cell lines. Zhou J; Ng AY; Tymms MJ; Jermiin LS; Seth AK; Thomas RS; Kola I Oncogene; 1998 Nov; 17(21):2719-32. PubMed ID: 9840936 [TBL] [Abstract][Full Text] [Related]
10. cDNA cloning, molecular characterization, and chromosomal localization of NET(EPHT2), a human EPH-related receptor protein-tyrosine kinase gene preferentially expressed in brain. Tang XX; Biegel JA; Nycum LM; Yoshioka A; Brodeur GM; Pleasure DE; Ikegaki N Genomics; 1995 Sep; 29(2):426-37. PubMed ID: 8666391 [TBL] [Abstract][Full Text] [Related]
11. The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous system. Gray TA; Hernandez L; Carey AH; Schaldach MA; Smithwick MJ; Rus K; Marshall Graves JA; Stewart CL; Nicholls RD Genomics; 2000 May; 66(1):76-86. PubMed ID: 10843807 [TBL] [Abstract][Full Text] [Related]
12. Emergence of a brain-expressed variant melanin-concentrating hormone gene during higher primate evolution: a gene "in search of a function". Viale A; Ortola C; Richard F; Vernier P; Presse F; Schilling S; Dutrillaux B; Nahon JL Mol Biol Evol; 1998 Feb; 15(2):196-214. PubMed ID: 9491616 [TBL] [Abstract][Full Text] [Related]
13. Altered trans-activational properties of a mutated WT1 gene product in a WAGR-associated Wilms' tumor. Park S; Tomlinson G; Nisen P; Haber DA Cancer Res; 1993 Oct; 53(20):4757-60. PubMed ID: 8402654 [TBL] [Abstract][Full Text] [Related]
14. A WAGR region gene between PAX-6 and FSHB expressed in fetal brain. Schwartz F; Neve R; Eisenman R; Gessler M; Bruns G Hum Genet; 1994 Dec; 94(6):658-64. PubMed ID: 7527372 [TBL] [Abstract][Full Text] [Related]
15. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism. Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215 [TBL] [Abstract][Full Text] [Related]
16. Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias. Lorda-Sanchez I; Sanz R; Diaz-Guillen MA; Fernandez-Toral J; Heine-Suñer D; Rodriguez De Alba M; Gonzalez-Gonzalez C; Trujillo MJ; Ramos C; Rodriguez De Cordoba S; Ayuso C Genet Couns; 2002; 13(2):171-7. PubMed ID: 12150218 [TBL] [Abstract][Full Text] [Related]
17. Characterization, chromosomal assignment, and tissue expression of a novel human gene belonging to the ARF GAP family. Zhang C; Yu Y; Zhang S; Liu M; Xing G; Wei H; Bi J; Liu X; Zhou G; Dong C; Hu Z; Zhang Y; Luo L; Wu C; Zhao S; He F Genomics; 2000 Feb; 63(3):400-8. PubMed ID: 10704287 [TBL] [Abstract][Full Text] [Related]
18. WAGR syndrome--a case report. Mahale A; Poornima V; Shrestha M Nepal Med Coll J; 2007 Jun; 9(2):138-40. PubMed ID: 17899969 [TBL] [Abstract][Full Text] [Related]
19. Characterization of a kinesin-related gene ATSV, within the tuberous sclerosis locus (TSC1) candidate region on chromosome 9Q34. Furlong RA; Zhou CY; Ferguson-Smith MA; Affara NA Genomics; 1996 May; 33(3):421-9. PubMed ID: 8661001 [TBL] [Abstract][Full Text] [Related]
20. Identification and characterization of NBEAL1, a novel human neurobeachin-like 1 protein gene from fetal brain, which is up regulated in glioma. Chen J; Lu Y; Xu J; Huang Y; Cheng H; Hu G; Luo C; Lou M; Cao G; Xie Y; Ying K Brain Res Mol Brain Res; 2004 Jun; 125(1-2):147-55. PubMed ID: 15193433 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]