Amir RE[au] - Search Results

Year	Number of Results
1999	2
2000	3
2002	1
2004	1
2005	2
2007	1
2008	4
2009	3
2010	1
2024	0

1

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Amir RE, et al. Nat Genet. 1999 Oct;23(2):185-8. doi: 10.1038/13810. Nat Genet. 1999. PMID: 10508514

2

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.

Amir RE, Zoghbi HY. Amir RE, et al. Am J Med Genet. 2000 Summer;97(2):147-52. doi: 10.1002/1096-8628(200022)97:2<147::aid-ajmg6>3.0.co;2-o. Am J Med Genet. 2000. PMID: 11180222 Review.

3

Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.

Amir RE, Sutton VR, Van den Veyver IB. Amir RE, et al. J Child Neurol. 2005 Sep;20(9):779-83. doi: 10.1177/08830738050200091401. J Child Neurol. 2005. PMID: 16225835 Review.

4

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB. Amir RE, et al. J Med Genet. 2005 Feb;42(2):e15. doi: 10.1136/jmg.2004.026161. J Med Genet. 2005. PMID: 15689438 Free PMC article. No abstract available.

5

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.

Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY. Amir RE, et al. Ann Neurol. 2000 May;47(5):670-9. Ann Neurol. 2000. PMID: 10805343

6

Serum oxidative stress level correlates with clinical parameters in chronic systolic heart failure patients.

Amir O, Paz H, Rogowski O, Barshai M, Sagiv M, Shnizer S, Reznick AZ, Amir RE. Amir O, et al. Among authors: amir re. Clin Cardiol. 2009 Apr;32(4):199-203. doi: 10.1002/clc.20317. Clin Cardiol. 2009. PMID: 19353709 Free PMC article.

7

The response of circulating brain natriuretic peptide to academic stress in college students.

Amir O, Sagiv M, Eynon N, Yamin C, Rogowski O, Gerzy Y, Amir RE. Amir O, et al. Among authors: amir re. Stress. 2010 Jan;13(1):83-90. doi: 10.3109/10253890902818357. Stress. 2010. PMID: 19658032

8

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots.

Wan M, Lee SS, Zhang X, Houwink-Manville I, Song HR, Amir RE, Budden S, Naidu S, Pereira JL, Lo IF, Zoghbi HY, Schanen NC, Francke U. Wan M, et al. Among authors: amir re. Am J Hum Genet. 1999 Dec;65(6):1520-9. doi: 10.1086/302690. Am J Hum Genet. 1999. PMID: 10577905 Free PMC article.

9

ACE ID genotype affects blood creatine kinase response to eccentric exercise.

Yamin C, Amir O, Sagiv M, Attias E, Meckel Y, Eynon N, Sagiv M, Amir RE. Yamin C, et al. Among authors: amir re. J Appl Physiol (1985). 2007 Dec;103(6):2057-61. doi: 10.1152/japplphysiol.00867.2007. Epub 2007 Sep 20. J Appl Physiol (1985). 2007. PMID: 17885020 Free article.

10

The NEDD8 pathway is essential for SCF(beta -TrCP)-mediated ubiquitination and processing of the NF-kappa B precursor p105.

Amir RE, Iwai K, Ciechanover A. Amir RE, et al. J Biol Chem. 2002 Jun 28;277(26):23253-9. doi: 10.1074/jbc.M200967200. Epub 2002 Apr 12. J Biol Chem. 2002. PMID: 11953428 Free article.

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