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The Journal of Investigative Dermatology
|
May 3, 2000
Desmosome assembly and keratin network formation after Ca2+/serum induction and UVB radiation in Hailey-Hailey keratinocytes
M Bernards, B P Korge
Journal of Molecular Medicine (Berlin, Germany)
|
February 1, 1996
The molecular basis for inherited bullous diseases
B P Korge, T Krieg
Journal of the American Academy of Dermatology
|
January 1, 1994
Keratin and keratinization
D P Smack, B P Korge, W D James
The Journal of Investigative Dermatology
|
November 6, 1998
Novel K5 and K14 mutations in German patients with the Weber-Cockayne variant of epidermolysis bullosa simplex
F B Müller, W Küster, L Bruckner-Tuderman, et al.
The Journal of Investigative Dermatology
|
December 1, 1992
The two size alleles of human keratin 1 are due to a deletion in the glycine-rich carboxyl-terminal V2 subdomain
B P Korge, J G Compton, P M Steinert, et al.
The Journal of Investigative Dermatology
|
June 26, 1999
A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case
F B Müller, I Anton-Lamprecht, W Küster, et al.
The Journal of Investigative Dermatology
|
May 1, 1996
Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21
D Mischke, B P Korge, I Marenholz, et al.
The Journal of Investigative Dermatology
|
October 1, 1993
Altered proliferation, synthetic activity, and differentiation of cultured human sebocytes in the absence of vitamin A and their modulation by synthetic retinoids
C C Zouboulis, B P Korge, D Mischke, et al.
The British Journal of Dermatology
|
May 13, 2005
A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay
F B Müller, A Tsianakas, C Kuwert, et al.
The Journal of Dermatology
|
November 1, 1992
The cornified cell envelope: loricrin and transglutaminases
K Yoneda, O W McBride, B P Korge, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
The Journal of Investigative Dermatology
|
May 3, 2000
Desmosome assembly and keratin network formation after Ca2+/serum induction and UVB radiation in Hailey-Hailey keratinocytes
M Bernards, B P Korge
Journal of Molecular Medicine (Berlin, Germany)
|
February 1, 1996
The molecular basis for inherited bullous diseases
B P Korge, T Krieg
Journal of the American Academy of Dermatology
|
January 1, 1994
Keratin and keratinization
D P Smack, B P Korge, W D James
The Journal of Investigative Dermatology
|
November 6, 1998
Novel K5 and K14 mutations in German patients with the Weber-Cockayne variant of epidermolysis bullosa simplex
F B Müller, W Küster, L Bruckner-Tuderman, et al.
The Journal of Investigative Dermatology
|
December 1, 1992
The two size alleles of human keratin 1 are due to a deletion in the glycine-rich carboxyl-terminal V2 subdomain
B P Korge, J G Compton, P M Steinert, et al.
The Journal of Investigative Dermatology
|
June 26, 1999
A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case
F B Müller, I Anton-Lamprecht, W Küster, et al.
The Journal of Investigative Dermatology
|
May 1, 1996
Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21
D Mischke, B P Korge, I Marenholz, et al.
The Journal of Investigative Dermatology
|
October 1, 1993
Altered proliferation, synthetic activity, and differentiation of cultured human sebocytes in the absence of vitamin A and their modulation by synthetic retinoids
C C Zouboulis, B P Korge, D Mischke, et al.
The British Journal of Dermatology
|
May 13, 2005
A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay
F B Müller, A Tsianakas, C Kuwert, et al.
The Journal of Dermatology
|
November 1, 1992
The cornified cell envelope: loricrin and transglutaminases
K Yoneda, O W McBride, B P Korge, et al.
Page
of 3