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American Journal of Physiology. Heart and Circulatory Physiology
|
April 12, 2001
Phenylarsine oxide induces mitochondrial permeability transition, hypercontracture, and cardiac cell death
P Korge, J I Goldhaber, J N Weiss
American Journal of Physiology. Cell Physiology
|
February 15, 2001
Regulation of the mitochondrial permeability transition by matrix Ca(2+) and voltage during anoxia/reoxygenation
P Korge, H M Honda, J N Weiss
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 4
Search research articles
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Showing results (11-20 of 35) with videos related to
Sort By:
Page
of 4
American Journal of Physiology. Heart and Circulatory Physiology
|
April 12, 2001
Phenylarsine oxide induces mitochondrial permeability transition, hypercontracture, and cardiac cell death
P Korge, J I Goldhaber, J N Weiss
American Journal of Physiology. Cell Physiology
|
February 15, 2001
Regulation of the mitochondrial permeability transition by matrix Ca(2+) and voltage during anoxia/reoxygenation
P Korge, H M Honda, J N Weiss
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 4