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Plos Genetics
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April 29, 2017
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation
Ethiraj Ravindran, Hao Hu, Scott A Yuzwa, et al.
Epilepsy Research
|
September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures
C Windemuth, H Schulz, K Saar, et al.
Nature Genetics
|
August 31, 2001
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
K Grohmann, M Schuelke, A Diers, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco
|
January 5, 2013
Lack of association of a functional catechol-O-methyltransferase gene polymorphism with risk of tobacco smoking: results from a multicenter case-control study
Jochen Mutschler, Elvira Abbruzzese, Christoph von der Goltz, et al.
Drug and Alcohol Dependence
|
August 28, 2024
Polygenic risk scores for nicotine use and family history of smoking are associated with smoking behaviour
Jerome C Foo, Maja P Völker, Fabian Streit, et al.
Addiction Biology
|
April 28, 2011
The German multi-centre study on smoking-related behavior-description of a population-based case-control study
Annette Lindenberg, Jürgen Brinkmeyer, Norbert Dahmen, et al.
Scientific Reports
|
April 15, 2024
Body composition impacts outcome of bronchoscopic lung volume reduction in patients with severe emphysema: a fully automated CT-based analysis
Johannes Wienker, Kaid Darwiche, Nele Rüsche, et al.
Nature Communications
|
February 24, 2026
Context-dependent translation inhibition as a cancer therapeutic modality
Paige D Diamond, Paul V Sauer, Mikael Holm, et al.
Annals of Nutrition & Metabolism
|
May 9, 2013
Functional polymorphism in the neuropeptide Y gene promoter (rs16147) is associated with serum leptin levels and waist-hip ratio in women
Jochen Mutschler, Elvira Abbruzzese, Klaus Wiedemann, et al.
European Journal of Oral Sciences
|
September 19, 2012
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate
Elisabeth Mangold, Heiko Reutter, Rafael B R León-Cachón, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 282) with videos related to
Sort By:
Page
of 29
Plos Genetics
|
April 29, 2017
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation
Ethiraj Ravindran, Hao Hu, Scott A Yuzwa, et al.
Epilepsy Research
|
September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures
C Windemuth, H Schulz, K Saar, et al.
Nature Genetics
|
August 31, 2001
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
K Grohmann, M Schuelke, A Diers, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco
|
January 5, 2013
Lack of association of a functional catechol-O-methyltransferase gene polymorphism with risk of tobacco smoking: results from a multicenter case-control study
Jochen Mutschler, Elvira Abbruzzese, Christoph von der Goltz, et al.
Drug and Alcohol Dependence
|
August 28, 2024
Polygenic risk scores for nicotine use and family history of smoking are associated with smoking behaviour
Jerome C Foo, Maja P Völker, Fabian Streit, et al.
Addiction Biology
|
April 28, 2011
The German multi-centre study on smoking-related behavior-description of a population-based case-control study
Annette Lindenberg, Jürgen Brinkmeyer, Norbert Dahmen, et al.
Scientific Reports
|
April 15, 2024
Body composition impacts outcome of bronchoscopic lung volume reduction in patients with severe emphysema: a fully automated CT-based analysis
Johannes Wienker, Kaid Darwiche, Nele Rüsche, et al.
Nature Communications
|
February 24, 2026
Context-dependent translation inhibition as a cancer therapeutic modality
Paige D Diamond, Paul V Sauer, Mikael Holm, et al.
Annals of Nutrition & Metabolism
|
May 9, 2013
Functional polymorphism in the neuropeptide Y gene promoter (rs16147) is associated with serum leptin levels and waist-hip ratio in women
Jochen Mutschler, Elvira Abbruzzese, Klaus Wiedemann, et al.
European Journal of Oral Sciences
|
September 19, 2012
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate
Elisabeth Mangold, Heiko Reutter, Rafael B R León-Cachón, et al.
Page
of 29