A Rahat
Overview
Explore the profile of A Rahat including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
319
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Recent Articles
1.
Ozeri-Galai E, Schwartz M, Rahat A, Kerem B
Oncogene
. 2007 Oct;
27(15):2109-17.
PMID: 17934520
Common fragile sites are specific genomic loci that form constrictions and gaps on metaphase chromosomes under conditions that slow, but do not arrest, DNA replication. These sites have been shown...
2.
Hellman A, Rahat A, Scherer S, Darvasi A, Tsui L, Kerem B
Mol Cell Biol
. 2000 May;
20(12):4420-7.
PMID: 10825205
Common fragile sites are specific chromosomal loci that show gaps, breaks, or rearrangements in metaphase chromosomes under conditions that interfere with DNA replication. The mechanism underlying the chromosomal instability at...
3.
Benhorin J, Goldmit M, Maccluer J, Blangero J, Goffen R, Leibovitch A, et al.
Hum Mutat
. 2000 Jan;
12(1):72.
PMID: 10627139
The long QT syndrome (LQT) is an inherited cardiac disorder that can cause sudden cardiac death among apparently healthy young individuals due to malignant ventricular arrhythmias. LQT was found to...
4.
Mishmar D, Margalit H, Rahat A, Kerem B
Am J Hum Genet
. 1999 Mar;
64(3):908-10.
PMID: 10053029
No abstract available.
5.
Chiba-Falek O, Kerem E, Shoshani T, Aviram M, Augarten A, Bentur L, et al.
Genomics
. 1998 Nov;
53(3):276-83.
PMID: 9799593
Disease severity varies among cystic fibrosis (CF) patients carrying the same CFTR genotype. Here we studied the mechanism underlying disease variability in individuals carrying a splicing CFTR mutation, 3849+10 kb...
6.
Mishmar D, Rahat A, Scherer S, Nyakatura G, Hinzmann B, Kohwi Y, et al.
Proc Natl Acad Sci U S A
. 1998 Jul;
95(14):8141-6.
PMID: 9653154
Common fragile sites are chromosomal loci prone to breakage and rearrangement, hypothesized to provide targets for foreign DNA integration. We cloned a simian virus 40 integration site and showed by...
7.
Kerem E, Madjar I, Goshen R, Augarten A, Rahat A, Hurwitz A, et al.
Am J Hum Genet
. 1997 Jan;
60(1):87-94.
PMID: 8981951
The splicing variant, 5T allele, in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene was shown to be associated with partial penetrance of the clinical expression. This...
8.
Madgar I, Goshen R, Ziadni A, Rahat A, Chiba O, Kalman Y, et al.
Am J Hum Genet
. 1995 Jun;
56(6):1359-66.
PMID: 7539210
Congenital bilateral aplasia of the vas deferens (CBAVD) was suggested to be a mild form of cystic fibrosis (CF). Mutation analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene...
9.
Davidov Y, Rahat A, FLECHNER I, Pines O
J Gen Microbiol
. 1993 Apr;
139(4):717-24.
PMID: 8515231
The rnc-97 mutation of the Escherichia coli double-stranded-RNA-specific ribonuclease III (RNAaseIII) was previously isolated by virtue of the lethal expression of RNAaseIII in Saccharomyces cerevisiae. Here we show that rnc-97...
10.
Rahat A, Stewart J, Blackwell C, WEIR D
Vox Sang
. 1990 Jan;
59(2):101-5.
PMID: 2238560
The amount of H antigens on buccal epithelial cells (BEC) of secretors and non-secretors was measured by flow cytometry. H type 1 and H type 2 on BEC were detected...