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Dora Angelicheva

Showing results (1-10 of 19) with videos related to

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Genetic Testing|February 26, 2008
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolatesSonja Bouwer, Dora Angelicheva, David Chandler, et al.
Biochemical and Biophysical Research Communications|June 1, 2005
NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24Michael Hunter, Dora Angelicheva, Ivailo Tournev, et al.
F1000Research|April 10, 2014
The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4DDavid Chandler, Sash Lopaticki, Dexing Huang, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Human Mutation|February 22, 2002
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian familiesMarie McCluskey, Tina Schiavello, Michael Hunter, et al.
Epilepsy Research|June 8, 2011
Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3Dimitar N Azmanov, Sashka Zhelyazkova, Melania Radionova, et al.
Epilepsy Research|September 16, 2011
A novel GEFS+ locus on 12p13.33 in a large Roma familyBharti Morar, Sashka Zhelyazkova, Dimitar N Azmanov, et al.
Plos One|March 27, 2012
Deleterious GRM1 mutations in schizophreniaMohammed Akli Ayoub, Dora Angelicheva, David Vile, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 30, 2008
Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder populationRadka Kaneva, Vihra Milanova, Dora Angelicheva, et al.
European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Genetic Testing|February 26, 2008
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolatesSonja Bouwer, Dora Angelicheva, David Chandler, et al.
Biochemical and Biophysical Research Communications|June 1, 2005
NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24Michael Hunter, Dora Angelicheva, Ivailo Tournev, et al.
F1000Research|April 10, 2014
The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4DDavid Chandler, Sash Lopaticki, Dexing Huang, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Human Mutation|February 22, 2002
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian familiesMarie McCluskey, Tina Schiavello, Michael Hunter, et al.
Epilepsy Research|June 8, 2011
Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3Dimitar N Azmanov, Sashka Zhelyazkova, Melania Radionova, et al.
Epilepsy Research|September 16, 2011
A novel GEFS+ locus on 12p13.33 in a large Roma familyBharti Morar, Sashka Zhelyazkova, Dimitar N Azmanov, et al.
Plos One|March 27, 2012
Deleterious GRM1 mutations in schizophreniaMohammed Akli Ayoub, Dora Angelicheva, David Vile, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 30, 2008
Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder populationRadka Kaneva, Vihra Milanova, Dora Angelicheva, et al.
European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
Pageof 2