Ezer S - Search Results

1

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: ezer s. Nat Genet. 1996 Aug;13(4):409-16. doi: 10.1038/ng0895-409. Nat Genet. 1996. PMID: 8696334

2

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. Hum Mol Genet. 1997 Sep;6(9):1581-7. doi: 10.1093/hmg/6.9.1581. Hum Mol Genet. 1997. PMID: 9285797

3

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. Among authors: ezer s. 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.

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: ezer s. 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: ezer s. Hum Mol Genet. 1998 Oct;7(11):1661-9. doi: 10.1093/hmg/7.11.1661. Hum Mol Genet. 1998. PMID: 9736768

6

Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin.

Montonen O, Ezer S, Laurikkala J, Karjalainen-Lindsberg ML, Thesleff I, Kere J, Saarialho-Kere U. Montonen O, et al. Among authors: ezer s. Exp Dermatol. 1998 Aug;7(4):168-74. doi: 10.1111/j.1600-0625.1998.tb00319.x. Exp Dermatol. 1998. PMID: 9758413

7

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells.

Ezer S, Bayés M, Elomaa O, Schlessinger D, Kere J. Ezer S, et al. Hum Mol Genet. 1999 Oct;8(11):2079-86. doi: 10.1093/hmg/8.11.2079. Hum Mol Genet. 1999. PMID: 10484778

8

Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.

Hannula-Jouppi K, Muurinen M, Lipsanen-Nyman M, Reinius LE, Ezer S, Greco D, Kere J. Hannula-Jouppi K, et al. Among authors: ezer s. Epigenetics. 2014 Mar;9(3):351-65. doi: 10.4161/epi.27160. Epub 2013 Nov 18. Epigenetics. 2014. PMID: 24247273 Free PMC article.

9

Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors.

Pulkkinen V, Ezer S, Sundman L, Hagström J, Remes S, Söderhäll C, Greco D, Haglund C, Kere J, Arola J. Pulkkinen V, et al. Among authors: ezer s. Virchows Arch. 2014 Aug;465(2):173-83. doi: 10.1007/s00428-014-1602-x. Epub 2014 Jun 12. Virchows Arch. 2014. PMID: 24915894 Free PMC article.

10

Generation of RNA sequencing libraries for transcriptome analysis of globin-rich tissues of the domestic dog.

Ezer S, Yoshihara M, Katayama S; DoGA consortium; Daub C, Lohi H, Krjutskov K, Kere J. Ezer S, et al. STAR Protoc. 2021 Dec 12;2(4):100995. doi: 10.1016/j.xpro.2021.100995. eCollection 2021 Dec 17. STAR Protoc. 2021. PMID: 34950881 Free PMC article.

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