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G Riley

Showing results (311-320 of 522) with videos related to

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Animal Bioscience|September 4, 2020
Genetic characteristics of Korean Jeju Black cattle with high density single nucleotide polymorphismsM Zahangir Alam, Yun-Mi Lee, Hyo-Jung Son, et al.
Plos One|August 14, 2014
Rapid identification of a novel complex I MT-ND3 m.10134C>A mutation in a Leigh syndrome patientDavid K Miller, Minal J Menezes, Cas Simons, et al.
Glycoconjugate Journal|September 29, 2006
UDP-Gal: GlcNAc-R beta1,4-galactosyltransferase--a target enzyme for drug design. Acceptor specificity and inhibition of the enzymeInka Brockhausen, Melinda Benn, Shridhar Bhat, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|September 19, 2003
The retention of 14C-labelled poly(acrylic acids) on gastric and oesophageal mucosa: an in vitro studyJohn D Smart, Robert G Riley, John Tsibouklis, et al.
Scientific Reports|May 6, 2021
A novel RLIM/RNF12 variant disrupts protein stability and function to cause severe Tonne-Kalscheuer syndromeFrancisco Bustos, Carmen Espejo-Serrano, Anna Segarra-Fas, et al.
Frontiers in Genetics|February 21, 2022
Skeletal Muscle Expression of Actinin-3 (<i>ACTN3</i>) in Relation to Feed Efficiency Phenotype of F<sub>2</sub> <i>Bos indicus</i> - <i>Bos taurus</i> SteersRobert N Vaughn, Kelli J Kochan, Aline K Torres, et al.
Journal of Animal Science|February 16, 2006
Effects of calpastatin and micro-calpain markers in beef cattle on tenderness traitsE Casas, S N White, T L Wheeler, et al.
Journal of Inherited Metabolic Disease|April 15, 2017
Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiencyS Balasubramaniam, L G Riley, D Bratkovic, et al.
Orphanet Journal of Rare Diseases|December 19, 2013
Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemiaLisa G Riley, Minal J Menezes, Joëlle Rudinger-Thirion, et al.
Clinical Genetics|February 28, 2024
A founder variant expands the phenotype of WNT7B-related PDAC syndromeLama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, et al.
Pageof 53

Showing results (311-320 of 522) with videos related to

Sort By:
Pageof 53
Animal Bioscience|September 4, 2020
Genetic characteristics of Korean Jeju Black cattle with high density single nucleotide polymorphismsM Zahangir Alam, Yun-Mi Lee, Hyo-Jung Son, et al.
Plos One|August 14, 2014
Rapid identification of a novel complex I MT-ND3 m.10134C>A mutation in a Leigh syndrome patientDavid K Miller, Minal J Menezes, Cas Simons, et al.
Glycoconjugate Journal|September 29, 2006
UDP-Gal: GlcNAc-R beta1,4-galactosyltransferase--a target enzyme for drug design. Acceptor specificity and inhibition of the enzymeInka Brockhausen, Melinda Benn, Shridhar Bhat, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|September 19, 2003
The retention of 14C-labelled poly(acrylic acids) on gastric and oesophageal mucosa: an in vitro studyJohn D Smart, Robert G Riley, John Tsibouklis, et al.
Scientific Reports|May 6, 2021
A novel RLIM/RNF12 variant disrupts protein stability and function to cause severe Tonne-Kalscheuer syndromeFrancisco Bustos, Carmen Espejo-Serrano, Anna Segarra-Fas, et al.
Frontiers in Genetics|February 21, 2022
Skeletal Muscle Expression of Actinin-3 (<i>ACTN3</i>) in Relation to Feed Efficiency Phenotype of F<sub>2</sub> <i>Bos indicus</i> - <i>Bos taurus</i> SteersRobert N Vaughn, Kelli J Kochan, Aline K Torres, et al.
Journal of Animal Science|February 16, 2006
Effects of calpastatin and micro-calpain markers in beef cattle on tenderness traitsE Casas, S N White, T L Wheeler, et al.
Journal of Inherited Metabolic Disease|April 15, 2017
Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiencyS Balasubramaniam, L G Riley, D Bratkovic, et al.
Orphanet Journal of Rare Diseases|December 19, 2013
Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemiaLisa G Riley, Minal J Menezes, Joëlle Rudinger-Thirion, et al.
Clinical Genetics|February 28, 2024
A founder variant expands the phenotype of WNT7B-related PDAC syndromeLama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, et al.
Pageof 53