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E H Epstein

Showing results (71-80 of 88) with videos related to

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The Journal of Investigative Dermatology|March 20, 1999
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of SiemensM J Arin, M A Longley, E H Epstein, et al.
Nature Genetics|December 30, 1999
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey diseaseZ Hu, J M Bonifas, J Beech, et al.
The Journal of Investigative Dermatology|November 11, 1992
Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12J M Bonifas, J W Bare, M A Chen, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
Ultraviolet B(UVB)-induced cox-2 expression in murine skin: an immunohistochemical studyM Athar, K P An, K D Morel, et al.
The Journal of Investigative Dermatology|June 10, 1998
Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndromeM Aszterbaum, A Rothman, R L Johnson, et al.
The Journal of Investigative Dermatology|May 12, 2001
Activation of expression of hedgehog target genes in basal cell carcinomasJ M Bonifas, S Pennypacker, P T Chuang, et al.
Archives of Dermatology|April 1, 1983
Mycosis fungoides of the mastoid, middle ear, and CNS. Literature review of mycosis fungoides of the CNSH S Zackheim, C F Lebo, P Wasserstein, et al.
The Journal of Investigative Dermatology|October 1, 1994
Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosisJ M Bonifas, K Matsumura, M A Chen, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Nature Genetics|March 1, 1994
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)D Aberdam, M F Galliano, J Vailly, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
The Journal of Investigative Dermatology|March 20, 1999
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of SiemensM J Arin, M A Longley, E H Epstein, et al.
Nature Genetics|December 30, 1999
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey diseaseZ Hu, J M Bonifas, J Beech, et al.
The Journal of Investigative Dermatology|November 11, 1992
Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12J M Bonifas, J W Bare, M A Chen, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
Ultraviolet B(UVB)-induced cox-2 expression in murine skin: an immunohistochemical studyM Athar, K P An, K D Morel, et al.
The Journal of Investigative Dermatology|June 10, 1998
Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndromeM Aszterbaum, A Rothman, R L Johnson, et al.
The Journal of Investigative Dermatology|May 12, 2001
Activation of expression of hedgehog target genes in basal cell carcinomasJ M Bonifas, S Pennypacker, P T Chuang, et al.
Archives of Dermatology|April 1, 1983
Mycosis fungoides of the mastoid, middle ear, and CNS. Literature review of mycosis fungoides of the CNSH S Zackheim, C F Lebo, P Wasserstein, et al.
The Journal of Investigative Dermatology|October 1, 1994
Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosisJ M Bonifas, K Matsumura, M A Chen, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Nature Genetics|March 1, 1994
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)D Aberdam, M F Galliano, J Vailly, et al.
Pageof 9