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P Propping

Showing results (111-120 of 270) with videos related to

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Human Genetics|September 1, 1997
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissueY Wang, W Friedl, C Lamberti, et al.
Developmental Neuroscience|January 1, 1991
Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?J Kappler, W Pötter, V Gieselmann, et al.
American Journal of Medical Genetics|July 25, 1997
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsiesO Steinlein, T Sander, J Stoodt, et al.
Human Molecular Genetics|September 1, 1994
Eleven novel germline mutations in the adenomatous polyposis coli (APC) geneR Paffenholz, M Mandl, R Caspari, et al.
Human Molecular Genetics|June 1, 1994
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosisM Mandl, M Kadmon, M Sengteller, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 1998
[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer]Y Wang, W Friedl, P Propping, et al.
Human Molecular Genetics|January 1, 1994
Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposisM Mandl, R Paffenholz, W Friedl, et al.
Human Genetics|April 1, 1989
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.
Brain Research|April 19, 1988
The shark GABA-benzodiazepine receptor: further evidence for a not so late phylogenetic appearance of the benzodiazepine receptorJ Hebebrand, W Friedl, R Reichelt, et al.
Pharmacogenetics|April 20, 1999
Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptorM Brüss, H Bönisch, M Bühlen, et al.
Pageof 27

Showing results (111-120 of 270) with videos related to

Sort By:
Pageof 27
Human Genetics|September 1, 1997
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissueY Wang, W Friedl, C Lamberti, et al.
Developmental Neuroscience|January 1, 1991
Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?J Kappler, W Pötter, V Gieselmann, et al.
American Journal of Medical Genetics|July 25, 1997
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsiesO Steinlein, T Sander, J Stoodt, et al.
Human Molecular Genetics|September 1, 1994
Eleven novel germline mutations in the adenomatous polyposis coli (APC) geneR Paffenholz, M Mandl, R Caspari, et al.
Human Molecular Genetics|June 1, 1994
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosisM Mandl, M Kadmon, M Sengteller, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 1998
[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer]Y Wang, W Friedl, P Propping, et al.
Human Molecular Genetics|January 1, 1994
Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposisM Mandl, R Paffenholz, W Friedl, et al.
Human Genetics|April 1, 1989
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.
Brain Research|April 19, 1988
The shark GABA-benzodiazepine receptor: further evidence for a not so late phylogenetic appearance of the benzodiazepine receptorJ Hebebrand, W Friedl, R Reichelt, et al.
Pharmacogenetics|April 20, 1999
Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptorM Brüss, H Bönisch, M Bühlen, et al.
Pageof 27