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E H Epstein

Showing results (51-60 of 88) with videos related to

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Oncogene|March 7, 2017
Differing tumor-suppressor functions of Arf and p53 in murine basal cell carcinoma initiation and progressionG Y Wang, C N Wood, J A Dolorito, et al.
Metabolism: Clinical and Experimental|October 1, 1970
Urinary excretion of 3',5'-AMP in syndromes considered refractory to parathyroid hormoneG D Aurbach, R Marcus, R N Winickoff, et al.
Skin Pharmacology and Applied Skin Physiology|October 13, 2001
Chemoprevention of basal cell carcinomas in the ptc1+/- mouse--green and black teaJ L Hebert, F Khugyani, M Athar, et al.
The Journal of Investigative Dermatology|October 1, 1995
Keratin 14 gene mutations in patients with epidermolysis bullosa simplexH Chen, J M Bonifas, K Matsumura, et al.
Journal of the American Academy of Dermatology|September 1, 1983
Topical carmustine (BCNU) for mycosis fungoides and related disorders: a 10-year experienceH S Zackheim, E H Epstein, N S McNutt, et al.
Experimental Dermatology|February 25, 2000
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosisM J Arin, M A Longley, E H Epstein, et al.
Genomics|June 11, 1992
Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridizationJ M Bonifas, J W Bare, E D Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987
Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosisJ M Bonifas, B J Morley, R E Oakey, et al.
Human Molecular Genetics|March 1, 1994
Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patientsJ M Bonifas, J W Bare, R L Kerschmann, et al.
The Journal of Investigative Dermatology|September 1, 1997
Partial dominance of a keratin 14 mutation in epidermolysis bullosa simplex--increased severity of disease in a homozygoteZ L Hu, L Smith, S Martins, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Oncogene|March 7, 2017
Differing tumor-suppressor functions of Arf and p53 in murine basal cell carcinoma initiation and progressionG Y Wang, C N Wood, J A Dolorito, et al.
Metabolism: Clinical and Experimental|October 1, 1970
Urinary excretion of 3',5'-AMP in syndromes considered refractory to parathyroid hormoneG D Aurbach, R Marcus, R N Winickoff, et al.
Skin Pharmacology and Applied Skin Physiology|October 13, 2001
Chemoprevention of basal cell carcinomas in the ptc1+/- mouse--green and black teaJ L Hebert, F Khugyani, M Athar, et al.
The Journal of Investigative Dermatology|October 1, 1995
Keratin 14 gene mutations in patients with epidermolysis bullosa simplexH Chen, J M Bonifas, K Matsumura, et al.
Journal of the American Academy of Dermatology|September 1, 1983
Topical carmustine (BCNU) for mycosis fungoides and related disorders: a 10-year experienceH S Zackheim, E H Epstein, N S McNutt, et al.
Experimental Dermatology|February 25, 2000
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosisM J Arin, M A Longley, E H Epstein, et al.
Genomics|June 11, 1992
Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridizationJ M Bonifas, J W Bare, E D Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987
Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosisJ M Bonifas, B J Morley, R E Oakey, et al.
Human Molecular Genetics|March 1, 1994
Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patientsJ M Bonifas, J W Bare, R L Kerschmann, et al.
The Journal of Investigative Dermatology|September 1, 1997
Partial dominance of a keratin 14 mutation in epidermolysis bullosa simplex--increased severity of disease in a homozygoteZ L Hu, L Smith, S Martins, et al.
Pageof 9