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B P Korge

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Proceedings of the National Academy of Sciences of the United States of America|February 1, 1992
Extensive size polymorphism of the human keratin 10 chain resides in the C-terminal V2 subdomain due to variable numbers and sizes of glycine loopsB P Korge, S Q Gan, O W McBride, et al.
Genomics|November 1, 1996
Genetic analysis of the epidermal differentiation complex (EDC) on human chromosome 1q21: chromosomal orientation, new markers, and a 6-Mb YAC contigI Marenholz, A Volz, A Ziegler, et al.
Genomics|October 1, 1993
Physical mapping of a functional cluster of epidermal differentiation genes on chromosome 1q21A Volz, B P Korge, J G Compton, et al.
The British Journal of Dermatology|January 22, 2003
Adrenomedullin: expression and possible role in human skin and hair growthF B Müller, S Müller-Röver, B P Korge, et al.
International Journal of Biological Macromolecules|June 1, 1991
Glycine loops in proteins: their occurrence in certain intermediate filament chains, loricrins and single-stranded RNA binding proteinsP M Steinert, J W Mack, B P Korge, et al.
The British Journal of Dermatology|April 16, 2002
Genetic analysis of a severe case of Netherton syndrome and application for prenatal testingF B Müller, I Hausser, D Berg, et al.
Cell|September 4, 1992
A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosisC C Chipev, B P Korge, N Markova, et al.
The Journal of Investigative Dermatology|September 1, 1995
Hailey-Hailey disease maps to a 5 cM interval on chromosome 3q21-q24G Richard, B P Korge, A R Wright, et al.
The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1992
Extensive size polymorphism of the human keratin 10 chain resides in the C-terminal V2 subdomain due to variable numbers and sizes of glycine loopsB P Korge, S Q Gan, O W McBride, et al.
Genomics|November 1, 1996
Genetic analysis of the epidermal differentiation complex (EDC) on human chromosome 1q21: chromosomal orientation, new markers, and a 6-Mb YAC contigI Marenholz, A Volz, A Ziegler, et al.
Genomics|October 1, 1993
Physical mapping of a functional cluster of epidermal differentiation genes on chromosome 1q21A Volz, B P Korge, J G Compton, et al.
The British Journal of Dermatology|January 22, 2003
Adrenomedullin: expression and possible role in human skin and hair growthF B Müller, S Müller-Röver, B P Korge, et al.
International Journal of Biological Macromolecules|June 1, 1991
Glycine loops in proteins: their occurrence in certain intermediate filament chains, loricrins and single-stranded RNA binding proteinsP M Steinert, J W Mack, B P Korge, et al.
The British Journal of Dermatology|April 16, 2002
Genetic analysis of a severe case of Netherton syndrome and application for prenatal testingF B Müller, I Hausser, D Berg, et al.
Cell|September 4, 1992
A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosisC C Chipev, B P Korge, N Markova, et al.
The Journal of Investigative Dermatology|September 1, 1995
Hailey-Hailey disease maps to a 5 cM interval on chromosome 3q21-q24G Richard, B P Korge, A R Wright, et al.
The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, et al.
Pageof 3