Konstantin Kadzhaev
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Explore the profile of Konstantin Kadzhaev including associated specialties, affiliations and a list of published articles.
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6
Citations
169
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Recent Articles
1.
Lindgren H, Honn M, Golovlev I, Kadzhaev K, Conlan W, Sjostedt A
Infect Immun
. 2009 Aug;
77(10):4429-36.
PMID: 19651867
We investigated the role of the 58-kDa FTT0918 protein in the iron metabolism of Francisella tularensis. The phenotypes of SCHU S4, a prototypic strain of F. tularensis subsp. tularensis, and...
2.
Kadzhaev K, Zingmark C, Golovliov I, Bolanowski M, Shen H, Conlan W, et al.
PLoS One
. 2009 May;
4(5):e5463.
PMID: 19424499
Background: Francisella tularensis is a highly virulent human pathogen. The most virulent strains belong to subspecies tularensis and these strains cause a sometimes fatal disease. Despite an intense recent research...
3.
Kohn L, Bowne S, Sullivan L, Daiger S, Burstedt M, Kadzhaev K, et al.
Eur J Hum Genet
. 2008 Dec;
17(5):651-5.
PMID: 19050727
The aim of this study was to identify and characterize the underlying molecular mechanisms in autosomal-dominant retinitis pigmentosa (adRP) with incomplete penetrance in two Swedish families. An extended genealogical study...
4.
Kohn L, Burstedt M, Jonsson F, Kadzhaev K, Haamer E, Sandgren O, et al.
Invest Ophthalmol Vis Sci
. 2008 Mar;
49(7):3172-7.
PMID: 18344446
Purpose: Bothnia dystrophy (BD) is an autosomal recessive retinitis pigmentosa (arRP) associated with the c.700C>T mutation in the RLBP1 gene. Testing of patients with BD has revealed the c.700C>T mutation...
5.
Kohn L, Kadzhaev K, Burstedt M, Haraldsson S, Sandgren O, Golovleva I
Adv Exp Med Biol
. 2008 Jan;
613:229-34.
PMID: 18188949
No abstract available.
6.
Kohn L, Kadzhaev K, Burstedt M, Haraldsson S, Hallberg B, Sandgren O, et al.
Eur J Hum Genet
. 2007 Mar;
15(6):664-71.
PMID: 17377520
Autosomal dominant cone dystrophy (CORD5) (MIM 600977) is a rare disease predominantly affecting cone photoreceptors. Here we refine the CORD5 locus previously mapped to 17p13 from 27 to 14.3 cM...