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B Dworniczak

Showing results (11-20 of 48) with videos related to

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Nucleic Acids Research|April 25, 1991
PCR detection of the PvuII (Ea) RFLP at the human phenylalanine hydroxylase (PAH) locusB Dworniczak, N Wedemeyer, A Eigel, et al.
Human Mutation|February 6, 1998
Identification of four novel mutations in the factor VIII gene: three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC)K Tavassoli, A Eigel, B Dworniczak, et al.
Human Genetics|April 1, 1995
Two polymorphic dinucleotide repeats in intron 44 of the dystrophin geneS Köchling, J T den Dunnen, B Dworniczak, et al.
Journal of Molecular Biology|June 20, 1987
RNA polymerase II of Drosophila. Relation of its 140,000 Mr subunit to the beta subunit of Escherichia coli RNA polymeraseD Falkenburg, B Dworniczak, D M Faust, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Demonstration of activated oncogenes of the ras family in human thyroid tumors using the polymerase chain reaction]B Dockhorn-Dworniczak, S Caspari, S Schröder, et al.
European Journal of Biochemistry|December 1, 1978
Identification of cysteine-10 of protein S18 as part of the mRNA-binding site of Escherichia coli ribosomes by affinity-labeling studies with a chemically reactive A-U-G analogM Yaguchi, E Lanka, B Dworniczak, et al.
Molecular Human Reproduction|December 28, 1999
No evidence for uniparental disomy of the sex chromosomes in idiopathic male infertilityD Meschede, B Dworniczak, H M Behre, et al.
Genomics|October 27, 1997
The genomic organization and the full coding region of the human PAX7 geneE Vorobyov, I Mertsalov, B Dockhorn-Dworniczak, et al.
Human Molecular Genetics|September 1, 1994
Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populationsS Byck, K Morgan, L Tyfield, et al.
Lancet (London, England)|November 21, 1992
Uniparental disomy with normal phenotypeB Dworniczak, B Koppers, G Kurlemann, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Nucleic Acids Research|April 25, 1991
PCR detection of the PvuII (Ea) RFLP at the human phenylalanine hydroxylase (PAH) locusB Dworniczak, N Wedemeyer, A Eigel, et al.
Human Mutation|February 6, 1998
Identification of four novel mutations in the factor VIII gene: three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC)K Tavassoli, A Eigel, B Dworniczak, et al.
Human Genetics|April 1, 1995
Two polymorphic dinucleotide repeats in intron 44 of the dystrophin geneS Köchling, J T den Dunnen, B Dworniczak, et al.
Journal of Molecular Biology|June 20, 1987
RNA polymerase II of Drosophila. Relation of its 140,000 Mr subunit to the beta subunit of Escherichia coli RNA polymeraseD Falkenburg, B Dworniczak, D M Faust, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Demonstration of activated oncogenes of the ras family in human thyroid tumors using the polymerase chain reaction]B Dockhorn-Dworniczak, S Caspari, S Schröder, et al.
European Journal of Biochemistry|December 1, 1978
Identification of cysteine-10 of protein S18 as part of the mRNA-binding site of Escherichia coli ribosomes by affinity-labeling studies with a chemically reactive A-U-G analogM Yaguchi, E Lanka, B Dworniczak, et al.
Molecular Human Reproduction|December 28, 1999
No evidence for uniparental disomy of the sex chromosomes in idiopathic male infertilityD Meschede, B Dworniczak, H M Behre, et al.
Genomics|October 27, 1997
The genomic organization and the full coding region of the human PAX7 geneE Vorobyov, I Mertsalov, B Dockhorn-Dworniczak, et al.
Human Molecular Genetics|September 1, 1994
Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populationsS Byck, K Morgan, L Tyfield, et al.
Lancet (London, England)|November 21, 1992
Uniparental disomy with normal phenotypeB Dworniczak, B Koppers, G Kurlemann, et al.
Pageof 5