Gelb BD - Search Results

1

Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation properties.

Zhao F, Satoda M, Licht JD, Hayashizaki Y, Gelb BD. Zhao F, et al. Among authors: gelb bd. J Biol Chem. 2001 Nov 2;276(44):40755-60. doi: 10.1074/jbc.M106284200. Epub 2001 Aug 24. J Biol Chem. 2001. PMID: 11522791 Free article.

2

Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21.

Satoda M, Pierpont ME, Diaz GA, Bornemeier RA, Gelb BD. Satoda M, et al. Among authors: gelb bd. Circulation. 1999 Jun 15;99(23):3036-42. doi: 10.1161/01.cir.99.23.3036. Circulation. 1999. PMID: 10368122

3

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.

Satoda M, Zhao F, Diaz GA, Burn J, Goodship J, Davidson HR, Pierpont ME, Gelb BD. Satoda M, et al. Among authors: gelb bd. Nat Genet. 2000 May;25(1):42-6. doi: 10.1038/75578. Nat Genet. 2000. PMID: 10802654

4

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. Oishi K, et al. Among authors: gelb bd. Mol Genet Metab. 2001 Jun;73(2):149-59. doi: 10.1006/mgme.2001.3184. Mol Genet Metab. 2001. PMID: 11386850

5

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation.

Zhao F, Weismann CG, Satoda M, Pierpont ME, Sweeney E, Thompson EM, Gelb BD. Zhao F, et al. Among authors: gelb bd. Am J Hum Genet. 2001 Oct;69(4):695-703. doi: 10.1086/323410. Epub 2001 Aug 14. Am J Hum Genet. 2001. PMID: 11505339 Free PMC article.

6

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.

Tartaglia M, Niemeyer CM, Fragale A, Song X, Buechner J, Jung A, Hählen K, Hasle H, Licht JD, Gelb BD. Tartaglia M, et al. Among authors: gelb bd. Nat Genet. 2003 Jun;34(2):148-50. doi: 10.1038/ng1156. Nat Genet. 2003. PMID: 12717436

7

Transcription factor Ap2delta associates with Ash2l and ALR, a trithorax family histone methyltransferase, to activate Hoxc8 transcription.

Tan CC, Sindhu KV, Li S, Nishio H, Stoller JZ, Oishi K, Puttreddy S, Lee TJ, Epstein JA, Walsh MJ, Gelb BD. Tan CC, et al. Among authors: gelb bd. Proc Natl Acad Sci U S A. 2008 May 27;105(21):7472-7. doi: 10.1073/pnas.0711896105. Epub 2008 May 21. Proc Natl Acad Sci U S A. 2008. PMID: 18495928 Free PMC article.

8

Genomic structure of and a cardiac promoter for the mouse carnitine palmitoyltransferase II gene.

Gelb BD. Gelb BD. Genomics. 1993 Dec;18(3):651-5. doi: 10.1016/s0888-7543(05)80368-4. Genomics. 1993. PMID: 8307575

9

Cathepsin K: isolation and characterization of the murine cDNA and genomic sequence, the homologue of the human pycnodysostosis gene.

Gelb BD, Moissoglu K, Zhang J, Martignetti JA, Brömme D, Desnick RJ. Gelb BD, et al. Biochem Mol Med. 1996 Dec;59(2):200-6. doi: 10.1006/bmme.1996.0088. Biochem Mol Med. 1996. PMID: 8986645

10

Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.

Diaz GA, Banikazemi M, Oishi K, Desnick RJ, Gelb BD. Diaz GA, et al. Among authors: gelb bd. Nat Genet. 1999 Jul;22(3):309-12. doi: 10.1038/10385. Nat Genet. 1999. PMID: 10391223

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