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Tom Walsh

Showing results (81-90 of 193) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
G3 (Bethesda, Md.)|April 2, 2024
Improved reference quality genome sequence of the plastic-degrading greater wax moth, Galleria mellonellaReginald Young, Khandaker Asif Ahmed, Leon Court, et al.
Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica|July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patientsSiobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
American Journal of Human Genetics|December 31, 2005
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing lossHashem Shahin, Tom Walsh, Tama Sobe, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2010
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencingTom Walsh, Ming K Lee, Silvia Casadei, et al.
Plos One|July 17, 2015
Correction: The Potential Distribution of Invading Helicoverpa armigera in North America: Is It Just a Matter of Time?Darren J Kriticos, Noboru Ota, William D Hutchison, et al.
Cold Spring Harbor Molecular Case Studies|August 24, 2016
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive diseaseSarah B Pierce, Suleyman Gulsuner, Gail A Stapleton, et al.
Journal of Invertebrate Pathology|May 20, 2018
Analysis of cross-resistance to Vip3 proteins in eight insect colonies, from four insect species, selected for resistance to Bacillus thuringiensis insecticidal proteinsJoaquín Gomis-Cebolla, Yuequin Wang, Yudong Quan, et al.
Pageof 20

Showing results (81-90 of 193) with videos related to

Sort By:
Pageof 20
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
G3 (Bethesda, Md.)|April 2, 2024
Improved reference quality genome sequence of the plastic-degrading greater wax moth, Galleria mellonellaReginald Young, Khandaker Asif Ahmed, Leon Court, et al.
Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica|July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patientsSiobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
American Journal of Human Genetics|December 31, 2005
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing lossHashem Shahin, Tom Walsh, Tama Sobe, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2010
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencingTom Walsh, Ming K Lee, Silvia Casadei, et al.
Plos One|July 17, 2015
Correction: The Potential Distribution of Invading Helicoverpa armigera in North America: Is It Just a Matter of Time?Darren J Kriticos, Noboru Ota, William D Hutchison, et al.
Cold Spring Harbor Molecular Case Studies|August 24, 2016
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive diseaseSarah B Pierce, Suleyman Gulsuner, Gail A Stapleton, et al.
Journal of Invertebrate Pathology|May 20, 2018
Analysis of cross-resistance to Vip3 proteins in eight insect colonies, from four insect species, selected for resistance to Bacillus thuringiensis insecticidal proteinsJoaquín Gomis-Cebolla, Yuequin Wang, Yudong Quan, et al.
Pageof 20