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S W Scherer

Showing results (151-160 of 164) with videos related to

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Nature|September 6, 2000
Colorectal carcinomas in mice lacking the catalytic subunit of PI(3)KgammaT Sasaki, J Irie-Sasaki, Y Horie, et al.
Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Nature Communications|December 6, 2019
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disordersL D'Abate, S Walker, R K C Yuen, et al.
Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Molecular Psychiatry|June 1, 2016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypesM N Loviglio, M Leleu, K Männik, et al.
Nature Genetics|May 1, 1997
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomasL Schmidt, F M Duh, F Chen, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Pageof 17

Showing results (151-160 of 164) with videos related to

Sort By:
Pageof 17
Nature|September 6, 2000
Colorectal carcinomas in mice lacking the catalytic subunit of PI(3)KgammaT Sasaki, J Irie-Sasaki, Y Horie, et al.
Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Nature Communications|December 6, 2019
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disordersL D'Abate, S Walker, R K C Yuen, et al.
Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Molecular Psychiatry|June 1, 2016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypesM N Loviglio, M Leleu, K Männik, et al.
Nature Genetics|May 1, 1997
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomasL Schmidt, F M Duh, F Chen, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Pageof 17