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Wienker

Showing results (171-180 of 282) with videos related to

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Chronic Respiratory Disease|June 11, 2025
Comparative analysis of pulmonary function decline in patients undergoing bronchoscopic lung volume reduction with endobronchial valves versus conservative treatment in emphysema management: A longitudinal coarsened exact matched analysisJohannes Wienker, Kaid Darwiche, Rüdiger Karpf-Wissel, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 19, 2008
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypesMarc Fatar, Mark Stroick, Michael Steffens, et al.
Human Molecular Genetics|October 6, 2011
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some lociHeike Singer, Maja Walier, Nicole Nüsgen, et al.
Journal of Clinical Microbiology|May 5, 2006
Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantationJuergen Loeffler, Michael Steffens, Eva-Maria Arlt, et al.
Diabetologia|April 28, 2007
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2K Hoffmann, M Mattheisen, S Dahm, et al.
American Journal of Human Genetics|October 16, 1999
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21K Grohmann, T F Wienker, K Saar, et al.
Human Genetics|September 27, 2003
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approachJohannes Schumacher, Andreas C J Otte, Tim Becker, et al.
Neurology|September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6T Sander, B Bockenkamp, T Hildmann, et al.
Stroke|September 26, 1997
Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactylyR Naraghi, H Schuster, H R Toka, et al.
Nature Genetics|May 1, 1996
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12H Schuster, T E Wienker, S Bähring, et al.
Pageof 29

Showing results (171-180 of 282) with videos related to

Sort By:
Pageof 29
Chronic Respiratory Disease|June 11, 2025
Comparative analysis of pulmonary function decline in patients undergoing bronchoscopic lung volume reduction with endobronchial valves versus conservative treatment in emphysema management: A longitudinal coarsened exact matched analysisJohannes Wienker, Kaid Darwiche, Rüdiger Karpf-Wissel, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 19, 2008
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypesMarc Fatar, Mark Stroick, Michael Steffens, et al.
Human Molecular Genetics|October 6, 2011
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some lociHeike Singer, Maja Walier, Nicole Nüsgen, et al.
Journal of Clinical Microbiology|May 5, 2006
Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantationJuergen Loeffler, Michael Steffens, Eva-Maria Arlt, et al.
Diabetologia|April 28, 2007
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2K Hoffmann, M Mattheisen, S Dahm, et al.
American Journal of Human Genetics|October 16, 1999
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21K Grohmann, T F Wienker, K Saar, et al.
Human Genetics|September 27, 2003
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approachJohannes Schumacher, Andreas C J Otte, Tim Becker, et al.
Neurology|September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6T Sander, B Bockenkamp, T Hildmann, et al.
Stroke|September 26, 1997
Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactylyR Naraghi, H Schuster, H R Toka, et al.
Nature Genetics|May 1, 1996
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12H Schuster, T E Wienker, S Bähring, et al.
Pageof 29