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Gayle B Collin

Showing results (21-30 of 44) with videos related to

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Clinical Dysmorphology|November 29, 2012
Differences in the clinical spectrum of two adolescent male patients with Alström syndromeVladimir Kuburović, Jan D Marshall, Gayle B Collin, et al.
Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Cells|April 16, 2020
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell LossGayle B Collin, Navdeep Gogna, Bo Chang, et al.
European Journal of Human Genetics : EJHG|December 16, 2010
Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alström syndromeInes Pereiro, Bethan E Hoskins, Jan D Marshall, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
International Journal of Molecular Medicine|May 29, 2008
Regulation of Alström syndrome gene expression during adipogenesis and its relationship with fat cell insulin sensitivitySara Romano, Gabriella Milan, Caterina Veronese, et al.
Clinical Endocrinology|January 17, 2007
Characterization of the IGF system in 15 patients with Alström syndromePietro Maffei, Mara Boschetti, Jan D Marshall, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Nature Genetics|April 10, 2002
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeGayle B Collin, Jan D Marshall, Akihiro Ikeda, et al.
Molecular & Cellular Proteomics : MCP|December 27, 2011
Proteomic analysis of mitotic RNA polymerase II reveals novel interactors and association with proteins dysfunctional in diseaseAndré Möller, Sheila Q Xie, Fabian Hosp, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Clinical Dysmorphology|November 29, 2012
Differences in the clinical spectrum of two adolescent male patients with Alström syndromeVladimir Kuburović, Jan D Marshall, Gayle B Collin, et al.
Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Cells|April 16, 2020
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell LossGayle B Collin, Navdeep Gogna, Bo Chang, et al.
European Journal of Human Genetics : EJHG|December 16, 2010
Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alström syndromeInes Pereiro, Bethan E Hoskins, Jan D Marshall, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
International Journal of Molecular Medicine|May 29, 2008
Regulation of Alström syndrome gene expression during adipogenesis and its relationship with fat cell insulin sensitivitySara Romano, Gabriella Milan, Caterina Veronese, et al.
Clinical Endocrinology|January 17, 2007
Characterization of the IGF system in 15 patients with Alström syndromePietro Maffei, Mara Boschetti, Jan D Marshall, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Nature Genetics|April 10, 2002
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeGayle B Collin, Jan D Marshall, Akihiro Ikeda, et al.
Molecular & Cellular Proteomics : MCP|December 27, 2011
Proteomic analysis of mitotic RNA polymerase II reveals novel interactors and association with proteins dysfunctional in diseaseAndré Möller, Sheila Q Xie, Fabian Hosp, et al.
Pageof 5