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Sandra Hanneken

Showing results (11-20 of 29) with videos related to

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European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Journal of the American Academy of Dermatology|March 21, 2006
Familial aggregation of alopecia areataBettina Blaumeiser, Ineke van der Goot, Rolf Fimmers, et al.
American Journal of Human Genetics|February 9, 2006
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseRegina C Betz, Laura Planko, Sibylle Eigelshoven, et al.
American Journal of Human Genetics|February 29, 2008
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26Axel M Hillmer, Antonia Flaquer, Sandra Hanneken, et al.
The Journal of Investigative Dermatology|February 25, 2011
Genetic variants in CTLA4 are strongly associated with alopecia areataKarsten K-G John, Felix F Brockschmidt, Silke Redler, et al.
The Journal of Investigative Dermatology|June 22, 2007
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic diseaseRegina C Betz, Jana Pforr, Antonia Flaquer, et al.
The Journal of Investigative Dermatology|September 18, 2014
Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamuraF Buket Basmanav, Günter Fritz, Gilles G Lestringant, et al.
Archives of Dermatological Research|November 6, 2012
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair lossHassnaa Mahmoudi, Silke Redler, Pattie Birch, et al.
Experimental Dermatology|June 17, 2016
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2Johannes Fischer, Franziska Degenhardt, Andrea Hofmann, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos diseaseF Buket Basmanav, Ana-Maria Oprisoreanu, Sandra M Pasternack, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Journal of the American Academy of Dermatology|March 21, 2006
Familial aggregation of alopecia areataBettina Blaumeiser, Ineke van der Goot, Rolf Fimmers, et al.
American Journal of Human Genetics|February 9, 2006
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseRegina C Betz, Laura Planko, Sibylle Eigelshoven, et al.
American Journal of Human Genetics|February 29, 2008
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26Axel M Hillmer, Antonia Flaquer, Sandra Hanneken, et al.
The Journal of Investigative Dermatology|February 25, 2011
Genetic variants in CTLA4 are strongly associated with alopecia areataKarsten K-G John, Felix F Brockschmidt, Silke Redler, et al.
The Journal of Investigative Dermatology|June 22, 2007
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic diseaseRegina C Betz, Jana Pforr, Antonia Flaquer, et al.
The Journal of Investigative Dermatology|September 18, 2014
Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamuraF Buket Basmanav, Günter Fritz, Gilles G Lestringant, et al.
Archives of Dermatological Research|November 6, 2012
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair lossHassnaa Mahmoudi, Silke Redler, Pattie Birch, et al.
Experimental Dermatology|June 17, 2016
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2Johannes Fischer, Franziska Degenhardt, Andrea Hofmann, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos diseaseF Buket Basmanav, Ana-Maria Oprisoreanu, Sandra M Pasternack, et al.
Pageof 3