B Kerem
Overview
Explore the profile of B Kerem including associated specialties, affiliations and a list of published articles.
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Articles
49
Citations
5573
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Recent Articles
1.
Petrova N, Kashirskaya N, Vasilyeva T, Timkovskaya E, Voronkova A, Shabalova L, et al.
J Cyst Fibros
. 2016 Mar;
15(3):e28-32.
PMID: 26948992
Cystic fibrosis (CF; OMIM #219700) is a common autosomal recessive disease. The spectrum and frequency of CFTR mutations vary significantly in different populations and ethnic groups. A genetic epidemiological study...
2.
Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E, et al.
J Cyst Fibros
. 2011 Jun;
10 Suppl 2:S86-102.
PMID: 21658649
Several diseases have been clinically or genetically related to cystic fibrosis (CF), but a consensus definition is lacking. Here, we present a proposal for consensus guidelines on cystic fibrosis transmembrane...
3.
Castellani C, Cuppens H, Macek Jr M, Cassiman J, Kerem E, Durie P, et al.
J Cyst Fibros
. 2008 May;
7(3):179-96.
PMID: 18456578
It is often challenging for the clinician interested in cystic fibrosis (CF) to interpret molecular genetic results, and to integrate them in the diagnostic process. The limitations of genotyping technology,...
4.
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...
5.
Bester A, Schwartz M, Schmidt M, Garrigue A, Hacein-Bey-Abina S, Cavazzana-Calvo M, et al.
Gene Ther
. 2006 Mar;
13(13):1057-9.
PMID: 16511518
Following gene therapy of SCID-X1 using murine leukemia virus (MLV) derived vector, two patients developed leukemia owing to an activating vector integration near the LMO2 gene. We found that these...
6.
Shalev R, Manor O, Kerem B, Ayali M, Badichi N, Friedlander Y, et al.
J Learn Disabil
. 2004 Oct;
34(1):59-65.
PMID: 15497272
Whereas current evidence attests to a genetic component in the etiology of dyslexia and attention-deficit/hyperactivity disorder (ADHD), little is known about the role of genetics in developmental dyscalculia (DC). The...
7.
Lerer B, Segman R, Hamdan A, Kanyas K, Karni O, Kohn Y, et al.
Mol Psychiatry
. 2003 Jun;
8(5):488-98.
PMID: 12808429
Schizophrenia is a complex neuropsychiatric disorder to which an as-yet-unknown number of genes contribute, interacting with each other and the environment. Linkage analyses have implicated several chromosomal regions as harboring...
8.
Zoossmann-Diskin A, Joel A, Liron M, Kerem B, Shohat M, Peleg L
Ann Hum Biol
. 2002 Mar;
29(2):142-75.
PMID: 11874621
Background: A considerable body of data has been accumulated since the 1960s on protein electrophoretic markers in the Jewish populations of Israel. However, in some Jewish communities and for some...
9.
Wilschanski M, Famini H, Strauss-Liviatan N, Rivlin J, Blau H, Bibi H, et al.
Eur Respir J
. 2001 Aug;
17(6):1208-15.
PMID: 11491166
The diagnosis of cystic fibrosis (CF) is based on characteristic clinical and laboratory findings. However, a subgroup of patients present with an atypical phenotype that comprises partial CF phenotype, borderline...
10.
Abriel H, Wehrens X, Benhorin J, Kerem B, Kass R
Circulation
. 2000 Aug;
102(8):921-5.
PMID: 10952963
Background: Multiple mutations of SCN5A, the gene that encodes the human Na(+) channel alpha-subunit, are linked to 1 form of the congenital long-QT syndrome (LQT-3). D1790G (DG), an LQT-3 mutation...