Srivastava A - Search Results

1

Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding.

Ezer S, Schlessinger D, Srivastava A, Kere J. Ezer S, et al. Among authors: srivastava a. Hum Mol Genet. 1997 Sep;6(9):1581-7. doi: 10.1093/hmg/6.9.1581. Hum Mol Genet. 1997. PMID: 9285797

2

EDA targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby EDA-A1 transgenic mice.

Cui CY, Durmowicz M, Tanaka TS, Hartung AJ, Tezuka T, Hashimoto K, Ko MS, Srivastava AK, Schlessinger D. Cui CY, et al. Hum Mol Genet. 2002 Jul 15;11(15):1763-73. doi: 10.1093/hmg/11.15.1763. Hum Mol Genet. 2002. PMID: 12095918

3

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.

Kere J, Srivastava AK, Montonen O, Zonana J, Thomas N, Ferguson B, Munoz F, Morgan D, Clarke A, Baybayan P, Chen EY, Ezer S, Saarialho-Kere U, de la Chapelle A, Schlessinger D. Kere J, et al. Among authors: srivastava ak. Nat Genet. 1996 Aug;13(4):409-16. doi: 10.1038/ng0895-409. Nat Genet. 1996. PMID: 8696334

4

The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone.

Montonen O, Ezer S, Saarialho-Kere UK, Herva R, Karjalainen-Lindsberg ML, Kaitila I, Schlessinger D, Srivastava AK, Thesleff I, Kere J. Montonen O, et al. Among authors: srivastava ak. J Histochem Cytochem. 1998 Mar;46(3):281-9. doi: 10.1177/002215549804600301. J Histochem Cytochem. 1998. PMID: 9487109

5

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats.

Bayés M, Hartung AJ, Ezer S, Pispa J, Thesleff I, Srivastava AK, Kere J. Bayés M, et al. Among authors: srivastava ak. Hum Mol Genet. 1998 Oct;7(11):1661-9. doi: 10.1093/hmg/7.11.1661. Hum Mol Genet. 1998. PMID: 9736768

6

The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia.

Pääkkönen K, Cambiaghi S, Novelli G, Ouzts LV, Penttinen M, Kere J, Srivastava AK. Pääkkönen K, et al. Among authors: srivastava ak. Hum Mutat. 2001 Apr;17(4):349. doi: 10.1002/humu.33. Hum Mutat. 2001. PMID: 11295832

7

Inducible mEDA-A1 transgene mediates sebaceous gland hyperplasia and differential formation of two types of mouse hair follicles.

Cui CY, Durmowicz M, Ottolenghi C, Hashimoto T, Griggs B, Srivastava AK, Schlessinger D. Cui CY, et al. Hum Mol Genet. 2003 Nov 15;12(22):2931-40. doi: 10.1093/hmg/ddg325. Epub 2003 Sep 23. Hum Mol Genet. 2003. PMID: 14506134

8

Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed.

Srivastava AK, Montonen O, Saarialho-Kere U, Chen E, Baybayan P, Pispa J, Limon J, Schlessinger D, Kere J. Srivastava AK, et al. Am J Hum Genet. 1996 Jan;58(1):126-32. Am J Hum Genet. 1996. PMID: 8554048 Free PMC article.

9

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.

Srivastava AK, Pispa J, Hartung AJ, Du Y, Ezer S, Jenks T, Shimada T, Pekkanen M, Mikkola ML, Ko MS, Thesleff I, Kere J, Schlessinger D. Srivastava AK, et al. Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13069-74. doi: 10.1073/pnas.94.24.13069. Proc Natl Acad Sci U S A. 1997. PMID: 9371801 Free PMC article.

10

Functional characterization of the promoter of the X-linked ectodermal dysplasia gene.

Pengue G, Srivastava AK, Kere J, Schlessinger D, Durmowicz MC. Pengue G, et al. Among authors: srivastava ak. J Biol Chem. 1999 Sep 10;274(37):26477-84. doi: 10.1074/jbc.274.37.26477. J Biol Chem. 1999. PMID: 10473608 Free article.

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