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N Blin

Showing results (111-120 of 153) with videos related to

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The American Journal of Gastroenterology|October 1, 1991
Breast cancer-associated protein pS2 expression in tumors of the biliary tractG Seitz, B Thelsinger, G Tomasetto, et al.
Pediatric Transplantation|July 10, 2013
Failure of bortezomib to cure acute antibody-mediated rejection in a non-compliant renal transplant patientA Ryckewaert, E Allain-Launay, A Moreau, et al.
Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
Human Genetics|January 1, 1991
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuriaJ Jaruzelska, K F Henriksen, F Güttler, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Loss of heterozygosity on chromosome 3, bands q24----qter, in a diploid meningiomaU Färber, G Schneider, U M Schrell, et al.
The EMBO Journal|December 1, 1991
Molecular characterization of the mouse beta 3-adrenergic receptor: relationship with the atypical receptor of adipocytesC Nahmias, N Blin, J M Elalouf, et al.
Cancer|September 1, 1993
Retrospective analysis of prognostic significance of the estrogen-inducible pS2 gene in male breast carcinomaI Kardaś, G Seitz, J Limon, et al.
Cytogenetics and Cell Genetics|January 1, 1996
A third P-domain peptide gene (TFF3), human intestinal trefoil factor, maps to 21q22.3H Schmitt, I Wundrack, S Beck, et al.
International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
Pageof 16

Showing results (111-120 of 153) with videos related to

Sort By:
Pageof 16
The American Journal of Gastroenterology|October 1, 1991
Breast cancer-associated protein pS2 expression in tumors of the biliary tractG Seitz, B Thelsinger, G Tomasetto, et al.
Pediatric Transplantation|July 10, 2013
Failure of bortezomib to cure acute antibody-mediated rejection in a non-compliant renal transplant patientA Ryckewaert, E Allain-Launay, A Moreau, et al.
Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
Human Genetics|January 1, 1991
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuriaJ Jaruzelska, K F Henriksen, F Güttler, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Loss of heterozygosity on chromosome 3, bands q24----qter, in a diploid meningiomaU Färber, G Schneider, U M Schrell, et al.
The EMBO Journal|December 1, 1991
Molecular characterization of the mouse beta 3-adrenergic receptor: relationship with the atypical receptor of adipocytesC Nahmias, N Blin, J M Elalouf, et al.
Cancer|September 1, 1993
Retrospective analysis of prognostic significance of the estrogen-inducible pS2 gene in male breast carcinomaI Kardaś, G Seitz, J Limon, et al.
Cytogenetics and Cell Genetics|January 1, 1996
A third P-domain peptide gene (TFF3), human intestinal trefoil factor, maps to 21q22.3H Schmitt, I Wundrack, S Beck, et al.
International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
Pageof 16