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B H Weber

Showing results (31-40 of 91) with videos related to

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Human Molecular Genetics|December 1, 1995
A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical featuresU Felbor, H Stöhr, T Amann, et al.
Human Genetics|November 9, 2000
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancerF Krämer, K White, M Kubbies, et al.
American Journal of Human Genetics|October 1, 1996
A somatic truncating mutation in BRCA2 in a sporadic breast tumorB H Weber, M Brohm, I Stec, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Refined mapping of the gene encoding the p127 kDa UV-damaged DNA-binding protein (DDB1) within 11q12-q13.1 and its exclusion in Best's vitelliform macular dystrophyH Stöhr, A Marquardt, A Rivera, et al.
Investigative Ophthalmology & Visual Science|May 1, 1997
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathiesU Felbor, D Doepner, U Schneider, et al.
Biochemical and Biophysical Research Communications|January 10, 1977
Modification of yeast 3-phosphoglycerate kinase: isolation and sequence determination of a nitrated active-site peptide and isolation of a carboxyl modified active-site peptideA D Bacharach, F S Markland, A Pellino, et al.
Science (New York, N.Y.)|April 5, 1996
Silk properties determined by gland-specific expression of a spider fibroin gene familyP A Guerette, D G Ginzinger, B H Weber, et al.
Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 2, 1998
The natural history of X-linked retinoschisisM T Roesch, C C Ewing, A E Gibson, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 12, 1998
[Familial juvenile macular dystrophy with congenital hypotrichosis capitis]M Becker, K Rohrschneider, W Tilgen, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|December 1, 1995
A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical featuresU Felbor, H Stöhr, T Amann, et al.
Human Genetics|November 9, 2000
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancerF Krämer, K White, M Kubbies, et al.
American Journal of Human Genetics|October 1, 1996
A somatic truncating mutation in BRCA2 in a sporadic breast tumorB H Weber, M Brohm, I Stec, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Refined mapping of the gene encoding the p127 kDa UV-damaged DNA-binding protein (DDB1) within 11q12-q13.1 and its exclusion in Best's vitelliform macular dystrophyH Stöhr, A Marquardt, A Rivera, et al.
Investigative Ophthalmology & Visual Science|May 1, 1997
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathiesU Felbor, D Doepner, U Schneider, et al.
Biochemical and Biophysical Research Communications|January 10, 1977
Modification of yeast 3-phosphoglycerate kinase: isolation and sequence determination of a nitrated active-site peptide and isolation of a carboxyl modified active-site peptideA D Bacharach, F S Markland, A Pellino, et al.
Science (New York, N.Y.)|April 5, 1996
Silk properties determined by gland-specific expression of a spider fibroin gene familyP A Guerette, D G Ginzinger, B H Weber, et al.
Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 2, 1998
The natural history of X-linked retinoschisisM T Roesch, C C Ewing, A E Gibson, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 12, 1998
[Familial juvenile macular dystrophy with congenital hypotrichosis capitis]M Becker, K Rohrschneider, W Tilgen, et al.
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