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P Propping

Showing results (161-170 of 270) with videos related to

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Neuroreport|September 8, 2000
The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsyK Haug, T Sander, K Hallmann, et al.
Annals of Neurology|December 16, 2000
Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosisA Heils, K Haug, W S Kunz, et al.
Human Genetics|November 1, 1986
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patientsP Propping, W Friedl, M Huschka, et al.
Psychiatry Research|July 24, 1998
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, M M Nöthen, J P Gustavsson, et al.
The Journal of Investigative Dermatology|March 7, 2001
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivationR Kruse, A Rütten, H R Hosseiny-Malayeri, et al.
The Pharmacogenomics Journal|April 6, 2005
Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug responseY Freudenberg-Hua, J Freudenberg, J Winantea, et al.
Journal of Medical Genetics|July 6, 2004
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndromeE Mangold, C Pagenstecher, M Leister, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|October 6, 2005
[Detection of germline mutations in the APC gene with the protein truncation test]Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, et al.
Endoscopy|April 3, 2009
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screeningR Hüneburg, F Lammert, C Rabe, et al.
Human Genetics|March 1, 1997
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 regionJ Deckert, M M Nöthen, S P Bryant, et al.
Pageof 27

Showing results (161-170 of 270) with videos related to

Sort By:
Pageof 27
Neuroreport|September 8, 2000
The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsyK Haug, T Sander, K Hallmann, et al.
Annals of Neurology|December 16, 2000
Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosisA Heils, K Haug, W S Kunz, et al.
Human Genetics|November 1, 1986
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patientsP Propping, W Friedl, M Huschka, et al.
Psychiatry Research|July 24, 1998
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, M M Nöthen, J P Gustavsson, et al.
The Journal of Investigative Dermatology|March 7, 2001
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivationR Kruse, A Rütten, H R Hosseiny-Malayeri, et al.
The Pharmacogenomics Journal|April 6, 2005
Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug responseY Freudenberg-Hua, J Freudenberg, J Winantea, et al.
Journal of Medical Genetics|July 6, 2004
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndromeE Mangold, C Pagenstecher, M Leister, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|October 6, 2005
[Detection of germline mutations in the APC gene with the protein truncation test]Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, et al.
Endoscopy|April 3, 2009
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screeningR Hüneburg, F Lammert, C Rabe, et al.
Human Genetics|March 1, 1997
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 regionJ Deckert, M M Nöthen, S P Bryant, et al.
Pageof 27