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J W Bare

Showing results (1-10 of 10) with videos related to

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Human Molecular Genetics|October 11, 1992
Dinucleotide repeat polymorphism at the D18S19 locusJ W Bare, A Rothman, E Epstein
Cancer Research|March 25, 1992
Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this siteJ W Bare, R V Lebo, E H Epstein
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.
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.
The Journal of Investigative Dermatology|December 1, 1993
Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-MacklinJ M Bonifas, J W Bare, M A Chen, et al.
The Journal of Investigative Dermatology|June 1, 1994
Hailey-Hailey disease is not allelic to Darier's diseaseE A Welsh, S Ikeda, A M Peluso, 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.
The Journal of Cell Biology|March 1, 1988
Drosophila nuclear lamin precursor Dm0 is translated from either of two developmentally regulated mRNA species apparently encoded by a single geneY Gruenbaum, Y Landesman, B Drees, et al.
Cancer Research|June 15, 1997
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumorsJ Xie, R L Johnson, X Zhang, et al.
Science (New York, N.Y.)|June 14, 1996
Human homolog of patched, a candidate gene for the basal cell nevus syndromeR L Johnson, A L Rothman, J Xie, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|October 11, 1992
Dinucleotide repeat polymorphism at the D18S19 locusJ W Bare, A Rothman, E Epstein
Cancer Research|March 25, 1992
Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this siteJ W Bare, R V Lebo, E H Epstein
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.
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.
The Journal of Investigative Dermatology|December 1, 1993
Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-MacklinJ M Bonifas, J W Bare, M A Chen, et al.
The Journal of Investigative Dermatology|June 1, 1994
Hailey-Hailey disease is not allelic to Darier's diseaseE A Welsh, S Ikeda, A M Peluso, 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.
The Journal of Cell Biology|March 1, 1988
Drosophila nuclear lamin precursor Dm0 is translated from either of two developmentally regulated mRNA species apparently encoded by a single geneY Gruenbaum, Y Landesman, B Drees, et al.
Cancer Research|June 15, 1997
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumorsJ Xie, R L Johnson, X Zhang, et al.
Science (New York, N.Y.)|June 14, 1996
Human homolog of patched, a candidate gene for the basal cell nevus syndromeR L Johnson, A L Rothman, J Xie, et al.
Pageof 1