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Michael F Wangler

Showing results (11-20 of 113) with videos related to

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Plos One|June 11, 2025
Drosophila models uncover substrate channeling effects on phospholipids and sphingolipids in peroxisomal biogenesis disordersMichael F Wangler, Yu-Hsin Chao, Mary Roth, et al.
Journal of Visualized Experiments : Jove|September 10, 2019
In Vivo Functional Study of Disease-associated Rare Human Variants Using DrosophilaJ Michael Harnish, Samantha L Deal, Hsiao-Tuan Chao, et al.
Protein & Cell|August 9, 2011
Antioxidant proteins TSA and PAG interact synergistically with Presenilin to modulate Notch signaling in DrosophilaMichael F Wangler, Lawrence T Reiter, Georgianna Zimm, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registryMichael F Wangler, Aimee S Chang, Kelle H Moley, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Distinguishing <i>PEX</i> gene variant severity for mild, severe, and atypical peroxisome biogenesis disorders in <i>Drosophila</i>Vanessa A Gomez, Oguz Kanca, Sharayu V Jangam, et al.
Neurology. Genetics|November 20, 2019
Digital necrosis in an infant with severe spinal muscular atrophyDiana Carrasco, Pilar Magoulas, Jennifer C Scull, et al.
Disease Models & Mechanisms|July 7, 2025
Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disordersVanessa A Gomez, Oguz Kanca, Sharayu V Jangam, et al.
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
G3 (Bethesda, Md.)|November 27, 2019
A Genetic Screen for Genes That Impact Peroxisomes in <i>Drosophila</i> Identifies Candidate Genes for Human DiseaseHillary K Graves, Sharayu Jangam, Kai Li Tan, et al.
American Journal of Medical Genetics. Part A|December 5, 2024
Subacute Neuropathy Post-Liver Transplantation in Zellweger Spectrum Disorder: A Case ReportClarissa Gonzalez, Madelyn J Cohen, Juhee Hong, et al.
Pageof 12

Showing results (11-20 of 113) with videos related to

Sort By:
Pageof 12
Plos One|June 11, 2025
Drosophila models uncover substrate channeling effects on phospholipids and sphingolipids in peroxisomal biogenesis disordersMichael F Wangler, Yu-Hsin Chao, Mary Roth, et al.
Journal of Visualized Experiments : Jove|September 10, 2019
In Vivo Functional Study of Disease-associated Rare Human Variants Using DrosophilaJ Michael Harnish, Samantha L Deal, Hsiao-Tuan Chao, et al.
Protein & Cell|August 9, 2011
Antioxidant proteins TSA and PAG interact synergistically with Presenilin to modulate Notch signaling in DrosophilaMichael F Wangler, Lawrence T Reiter, Georgianna Zimm, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registryMichael F Wangler, Aimee S Chang, Kelle H Moley, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Distinguishing <i>PEX</i> gene variant severity for mild, severe, and atypical peroxisome biogenesis disorders in <i>Drosophila</i>Vanessa A Gomez, Oguz Kanca, Sharayu V Jangam, et al.
Neurology. Genetics|November 20, 2019
Digital necrosis in an infant with severe spinal muscular atrophyDiana Carrasco, Pilar Magoulas, Jennifer C Scull, et al.
Disease Models & Mechanisms|July 7, 2025
Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disordersVanessa A Gomez, Oguz Kanca, Sharayu V Jangam, et al.
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
G3 (Bethesda, Md.)|November 27, 2019
A Genetic Screen for Genes That Impact Peroxisomes in <i>Drosophila</i> Identifies Candidate Genes for Human DiseaseHillary K Graves, Sharayu Jangam, Kai Li Tan, et al.
American Journal of Medical Genetics. Part A|December 5, 2024
Subacute Neuropathy Post-Liver Transplantation in Zellweger Spectrum Disorder: A Case ReportClarissa Gonzalez, Madelyn J Cohen, Juhee Hong, et al.
Pageof 12