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American Journal of Human Genetics|July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36K Bosse, R C Betz, Y A Lee, et al.
The British Journal of Dermatology|January 4, 2012
FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasiaG Naz, S M Pasternack, C Perrin, et al.
Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.
Oncogene|December 21, 2010
Genome-wide shRNA screen reveals increased mitochondrial dependence upon mTORC2 addictionM Colombi, K D Molle, D Benjamin, et al.
The Journal of Experimental Medicine|April 28, 2010
Batf coordinates multiple aspects of B and T cell function required for normal antibody responsesBriana C Betz, Kimberly L Jordan-Williams, Chuanwu Wang, et al.
The Journal of Investigative Dermatology|June 19, 2009
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growthSandra M Pasternack, Ivar von Kügelgen, Melanie Müller, et al.
Archives of Dermatological Research|March 21, 2007
Identification of mutations in the human hairless gene in two new families with congenital atrichiaRegina C Betz, Margarita Indelman, Jana Pforr, et al.
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.
Physical Review Letters|September 26, 2012
Hot electron cooling by acoustic phonons in grapheneA C Betz, F Vialla, D Brunel, et al.
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