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Belinda Whittle

Showing results (1-10 of 39) with videos related to

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Journal of Alzheimer'S Disease : JAD|April 24, 2013
Single nucleotide variants (SNVs) define senescence-accelerated SAMP8 mice, a model of a geriatric conditionFabien Delerue, Geoff Sjollema, Belinda Whittle, et al.
BMC Clinical Pathology|July 10, 2015
The use of dried blood spot sampling for the measurement of HbA1c: a cross-sectional studyClaudio A Mastronardi, Belinda Whittle, Robert Tunningley, et al.
American Journal of Medical Genetics. Part A|May 2, 2015
A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner syndromeSophie Dunkerton, Matthew Field, Vicki Cho, et al.
Journal of Biomedicine & Biotechnology|January 6, 2012
ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant miceXin Liu, Michael Dobbie, Rob Tunningley, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|October 16, 2010
Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of diseaseNhung Nguyen, Louise M Judd, Anastasia Kalantzis, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 19, 2021
Direct measurement of pregnanediol 3-glucuronide (PDG) in dried urine spots by liquid chromatography-mass spectrometry to detect ovulationDavid J Handelsman, Rama Nimmagadda, Reena Desai, et al.
Immunology and Cell Biology|September 2, 2009
Mouse strains with point mutations in TAP1 and TAP2Angelo Theodoratos, Belinda Whittle, Anselm Enders, et al.
Plos One|November 9, 2013
A missense mutation in the transcription factor ETV5 leads to sterility, increased embryonic and perinatal death, postnatal growth restriction, renal asymmetry and polydactyly in the mouseDuangporn Jamsai, Brett J Clark, Stephanie J Smith, et al.
Bioinformatics (Oxford, England)|March 11, 2015
Reducing the search space for causal genetic variants with VASPMatthew A Field, Vicky Cho, Matthew C Cook, et al.
Human Genome Variation|April 16, 2016
A deleterious RNF43 germline mutation in a severely affected serrated polyposis kindredDouglas Taupin, Wesley Lam, David Rangiah, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Journal of Alzheimer'S Disease : JAD|April 24, 2013
Single nucleotide variants (SNVs) define senescence-accelerated SAMP8 mice, a model of a geriatric conditionFabien Delerue, Geoff Sjollema, Belinda Whittle, et al.
BMC Clinical Pathology|July 10, 2015
The use of dried blood spot sampling for the measurement of HbA1c: a cross-sectional studyClaudio A Mastronardi, Belinda Whittle, Robert Tunningley, et al.
American Journal of Medical Genetics. Part A|May 2, 2015
A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner syndromeSophie Dunkerton, Matthew Field, Vicki Cho, et al.
Journal of Biomedicine & Biotechnology|January 6, 2012
ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant miceXin Liu, Michael Dobbie, Rob Tunningley, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|October 16, 2010
Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of diseaseNhung Nguyen, Louise M Judd, Anastasia Kalantzis, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 19, 2021
Direct measurement of pregnanediol 3-glucuronide (PDG) in dried urine spots by liquid chromatography-mass spectrometry to detect ovulationDavid J Handelsman, Rama Nimmagadda, Reena Desai, et al.
Immunology and Cell Biology|September 2, 2009
Mouse strains with point mutations in TAP1 and TAP2Angelo Theodoratos, Belinda Whittle, Anselm Enders, et al.
Plos One|November 9, 2013
A missense mutation in the transcription factor ETV5 leads to sterility, increased embryonic and perinatal death, postnatal growth restriction, renal asymmetry and polydactyly in the mouseDuangporn Jamsai, Brett J Clark, Stephanie J Smith, et al.
Bioinformatics (Oxford, England)|March 11, 2015
Reducing the search space for causal genetic variants with VASPMatthew A Field, Vicky Cho, Matthew C Cook, et al.
Human Genome Variation|April 16, 2016
A deleterious RNF43 germline mutation in a severely affected serrated polyposis kindredDouglas Taupin, Wesley Lam, David Rangiah, et al.
Pageof 4