Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Frank Peelman

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
EMBO Molecular Medicine|January 9, 2020
Safe eradication of large established tumors using neovasculature-targeted tumor necrosis factor-based therapiesLeander Huyghe, Alexander Van Parys, Anje Cauwels, et al.
Chemistry & Biology|June 25, 2009
Chemical inhibition of a subset of Arabidopsis thaliana GSK3-like kinases activates brassinosteroid signalingBert De Rybel, Dominique Audenaert, Grégory Vert, et al.
Molecular Metabolism|April 17, 2024
Crosstalk interactions between transcription factors ERRα and PPARα assist PPARα-mediated gene expressionSofie J Desmet, Jonathan Thommis, Tineke Vanderhaeghen, et al.
The Journal of Allergy and Clinical Immunology|February 11, 2018
Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritisKeith A Sikora, Joshua R Bennett, Laurens Vyncke, et al.
Cellular and Molecular Life Sciences : CMLS|August 8, 2014
Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction levelLennart Zabeau, Cathy J Jensen, Sylvie Seeuws, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex developmentDorien Baetens, Tülay Güran, Berenice B Mendonca, et al.
American Journal of Human Genetics|August 4, 2016
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in UbiquitinationFrauke Coppieters, Giulia Ascari, Katharina Dannhausen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2018
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal diseaseStijn Van de Sompele, Claire Smith, Marianthi Karali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2019
Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal diseaseStijn Van de Sompele, Claire Smith, Marianthi Karali, et al.
Human Mutation|January 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertilityGiulia Ascari, Frank Peelman, Pietro Farinelli, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
EMBO Molecular Medicine|January 9, 2020
Safe eradication of large established tumors using neovasculature-targeted tumor necrosis factor-based therapiesLeander Huyghe, Alexander Van Parys, Anje Cauwels, et al.
Chemistry & Biology|June 25, 2009
Chemical inhibition of a subset of Arabidopsis thaliana GSK3-like kinases activates brassinosteroid signalingBert De Rybel, Dominique Audenaert, Grégory Vert, et al.
Molecular Metabolism|April 17, 2024
Crosstalk interactions between transcription factors ERRα and PPARα assist PPARα-mediated gene expressionSofie J Desmet, Jonathan Thommis, Tineke Vanderhaeghen, et al.
The Journal of Allergy and Clinical Immunology|February 11, 2018
Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritisKeith A Sikora, Joshua R Bennett, Laurens Vyncke, et al.
Cellular and Molecular Life Sciences : CMLS|August 8, 2014
Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction levelLennart Zabeau, Cathy J Jensen, Sylvie Seeuws, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex developmentDorien Baetens, Tülay Güran, Berenice B Mendonca, et al.
American Journal of Human Genetics|August 4, 2016
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in UbiquitinationFrauke Coppieters, Giulia Ascari, Katharina Dannhausen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2018
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal diseaseStijn Van de Sompele, Claire Smith, Marianthi Karali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2019
Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal diseaseStijn Van de Sompele, Claire Smith, Marianthi Karali, et al.
Human Mutation|January 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertilityGiulia Ascari, Frank Peelman, Pietro Farinelli, et al.
Pageof 7