H H Kazazian
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Explore the profile of H H Kazazian including associated specialties, affiliations and a list of published articles.
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28
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1073
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Recent Articles
1.
Vnencak-Jones C, Phillips III J, Janco R, Cohen M, Dupont W, Kazazian H, et al.
Haemophilia
. 2016 May;
2(1):18-23.
PMID: 27213900
Haemophilia A is an X-linked recessive bleeding disorder of variable severity that is caused by a deficiency of coagulation factor VIII (FVIII). The disease results from mutations in the FVIII...
2.
Kazazian H
Dev Biol (Basel)
. 2002 Jan;
106:307-13; discussion 313-4, 317-29.
PMID: 11761245
No abstract available.
3.
Haas N, Grabowski J, North J, Moran J, Kazazian H, Burch J
Gene
. 2001 Mar;
265(1-2):175-83.
PMID: 11255020
CR1 elements and CR1-related (CR1-like) elements are a novel family of non-LTR retrotransposons that are found in all vertebrates (reptilia, amphibia, fish, and mammals), whereas more distantly related elements are...
4.
Wei W, Gilbert N, Ooi S, Lawler J, Ostertag E, Kazazian H, et al.
Mol Cell Biol
. 2001 Feb;
21(4):1429-39.
PMID: 11158327
Long interspersed nuclear elements (LINEs or L1s) comprise approximately 17% of human DNA; however, only about 60 of the approximately 400,000 L1s are mobile. Using a retrotransposition assay in cultured...
5.
Pulver A, Mulle J, Nestadt G, Swartz K, Blouin J, Dombroski B, et al.
Mol Psychiatry
. 2000 Dec;
5(6):650-3.
PMID: 11126395
Despite considerable effort to identify susceptibility loci for schizophrenia, none have been localized. Multiple genome scans and collaborative efforts have shown evidence for linkage to regions on chromosomes 1q, 5q,...
6.
Antonarakis S, Blouin J, Lasseter V, Gehrig C, Radhakrishna U, Nestadt G, et al.
Am J Med Genet
. 1999 Jul;
88(4):348-51.
PMID: 10402501
To determine the importance of a candidate gene KCNN3 (formerly named hSKCa3) in the susceptibility to schizophrenia, we have studied the genotypes of a (CAG)n polymorphism within this gene in...
7.
Theophilus B, Enayat M, Higuchi M, Kazazian H, Antonarakis S, Hill F
Hum Mutat
. 1999 Apr;
11(4):334.
PMID: 10215414
Using chemical mismatch analysis or denaturing gradient gel electrophoresis followed by nucleotide sequencing, we have identified the same G6545A mutation leading to an Arg2163 His subsitution in the factor VIII...
8.
Curtis L, Blouin J, Radhakrishna U, Gehrig C, Lasseter V, Wolyniec P, et al.
Am J Med Genet
. 1999 Apr;
88(2):109-12.
PMID: 10206225
Freedman et al. [1997: Proc Natl Acad Sci USA 94:587-592] reported linkage in nine multiplex schizophrenia families to markers on chromosome 15, using impaired neuronal inhibition to repeated auditory stimuli...
9.
Blouin J, Dombroski B, Nath S, Lasseter V, Wolyniec P, Nestadt G, et al.
Nat Genet
. 1998 Sep;
20(1):70-3.
PMID: 9731535
Schizophrenia is a common disorder characterized by psychotic symptoms; diagnostic criteria have been established. Family, twin and adoption studies suggest that both genetic and environmental factors influence susceptibility (heritability is...
10.
Karayiorgou M, Gogos J, Galke B, Wolyniec P, Nestadt G, Antonarakis S, et al.
Biol Psychiatry
. 1998 Apr;
43(6):425-31.
PMID: 9532347
Background: Deletions of 1.5-2 MB of chromosome 22q11 have been previously associated with schizophrenia. The deleted region includes proximally the region harboring genes involved in DiGeorge and velocardiofacial syndromes. Distally,...