1273 related articles for article (PubMed ID: 11414760)
21. Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Guris DL; Fantes J; Tara D; Druker BJ; Imamoto A
Nat Genet; 2001 Mar; 27(3):293-8. PubMed ID: 11242111
[TBL] [Abstract][Full Text] [Related]
22. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
23. Cloning and characterization of human and mouse mitochondrial elongation factor G, GFM and Gfm, and mapping of GFM to human chromosome 3q25.1-q26.2.
Gao J; Yu L; Zhang P; Jiang J; Chen J; Peng J; Wei Y; Zhao S
Genomics; 2001 May; 74(1):109-14. PubMed ID: 11374907
[TBL] [Abstract][Full Text] [Related]
24. Slc19a2: cloning and characterization of the murine thiamin transporter cDNA and genomic sequence, the orthologue of the human TRMA gene.
Oishi K; Hirai T; Gelb BD; Diaz GA
Mol Genet Metab; 2001 Jun; 73(2):149-59. PubMed ID: 11386850
[TBL] [Abstract][Full Text] [Related]
25. Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23.
Holmes DI; Wahab NA; Mason RM
Genomics; 1999 Aug; 60(1):105-9. PubMed ID: 10458916
[TBL] [Abstract][Full Text] [Related]
26. Cloning, mapping, and characterization of the human sorbin and SH3 domain containing 1 (SORBS1) gene: a protein associated with c-Abl during insulin signaling in the hepatoma cell line Hep3B.
Lin WH; Huang CJ; Liu MW; Chang HM; Chen YJ; Tai TY; Chuang LM
Genomics; 2001 May; 74(1):12-20. PubMed ID: 11374898
[TBL] [Abstract][Full Text] [Related]
27. Isolation, characterization, and mapping of the mouse and human WDR8 genes, members of a novel WD-repeat gene family.
Koshizuka Y; Ikegawa S; Sano M; Nakamura K; Nakamura Y
Genomics; 2001 Mar; 72(3):252-9. PubMed ID: 11401440
[TBL] [Abstract][Full Text] [Related]
28. The novel human HUEL (C4orf1) gene maps to chromosome 4p12-p13 and encodes a nuclear protein containing the nuclear receptor interaction motif.
Sim DL; Chow VT
Genomics; 1999 Jul; 59(2):224-33. PubMed ID: 10409434
[TBL] [Abstract][Full Text] [Related]
29. claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing.
Niimi T; Nagashima K; Ward JM; Minoo P; Zimonjic DB; Popescu NC; Kimura S
Mol Cell Biol; 2001 Nov; 21(21):7380-90. PubMed ID: 11585919
[TBL] [Abstract][Full Text] [Related]
30. Characterization of the human TESTIN gene localized in the FRA7G region at 7q31.2.
Tatarelli C; Linnenbach A; Mimori K; Croce CM
Genomics; 2000 Aug; 68(1):1-12. PubMed ID: 10950921
[TBL] [Abstract][Full Text] [Related]
31. The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
Wilming LG; Snoeren CA; van Rijswijk A; Grosveld F; Meijers C
Hum Mol Genet; 1997 Feb; 6(2):247-58. PubMed ID: 9063745
[TBL] [Abstract][Full Text] [Related]
32. Characterization of the gene EPAC2: structure, chromosomal localization, tissue expression, and identification of the liver-specific isoform.
Ueno H; Shibasaki T; Iwanaga T; Takahashi K; Yokoyama Y; Liu LM; Yokoi N; Ozaki N; Matsukura S; Yano H; Seino S
Genomics; 2001 Nov; 78(1-2):91-8. PubMed ID: 11707077
[TBL] [Abstract][Full Text] [Related]
33. Isolation, tissue distribution, and chromosomal localization of the human activation-induced cytidine deaminase (AID) gene.
Muto T; Muramatsu M; Taniwaki M; Kinoshita K; Honjo T
Genomics; 2000 Aug; 68(1):85-8. PubMed ID: 10950930
[TBL] [Abstract][Full Text] [Related]
34. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.
Gorman SW; Haider NB; Grieshammer U; Swiderski RE; Kim E; Welch JW; Searby C; Leng S; Carmi R; Sheffield VC; Duhl DM
Genomics; 1999 Jul; 59(2):150-60. PubMed ID: 10409426
[TBL] [Abstract][Full Text] [Related]
35. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.
Daw SC; Taylor C; Kraman M; Call K; Mao J; Schuffenhauer S; Meitinger T; Lipson T; Goodship J; Scambler P
Nat Genet; 1996 Aug; 13(4):458-60. PubMed ID: 8696341
[TBL] [Abstract][Full Text] [Related]
36. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
Stalmans I
Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
[TBL] [Abstract][Full Text] [Related]
37. Molecular characterization and chromosomal assignment of the bovine glycinamide ribonucleotide formyltransferase (GART) gene on cattle chromosome 1q12.1-q12.2.
Wöhlke A; Drögemüller C; Kuiper H; Leeb T; Distl O
Gene; 2005 Mar; 348():73-81. PubMed ID: 15777723
[TBL] [Abstract][Full Text] [Related]
38. Cloning, expression pattern and essentiality of the high-affinity copper transporter 1 (ctr1) gene in zebrafish.
Mackenzie NC; Brito M; Reyes AE; Allende ML
Gene; 2004 Mar; 328():113-20. PubMed ID: 15019990
[TBL] [Abstract][Full Text] [Related]
39. Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5.
Orti R; Rachidi M; Vialard F; Toyama K; Lopes C; Taudien S; Rosenthal A; Yaspo ML; Sinet PM; Delabar JM
Genomics; 2000 Mar; 64(2):203-10. PubMed ID: 10729227
[TBL] [Abstract][Full Text] [Related]
40. Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L).
Botta A; Tandoi C; Fini G; Calabrese G; Dallapiccola B; Novelli G
Gene; 2001 Sep; 275(1):39-46. PubMed ID: 11574150
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
