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

Susan Marschall

Showing results (41-50 of 52) with videos related to

Pageof 6
Sort By:
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 9, 2023
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in miceManuela A Oestereicher, Janine M Wotton, Shinya Ayabe, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.
American Journal of Human Genetics|July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth diseaseDaniel G Calame, Tianyu Guo, Chen Wang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2012
The mammalian gene function resource: the International Knockout Mouse ConsortiumAllan Bradley, Konstantinos Anastassiadis, Abdelkader Ayadi, et al.
Nature|September 15, 2016
High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature Cardiovascular Research|April 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
Nature|November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 9, 2023
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in miceManuela A Oestereicher, Janine M Wotton, Shinya Ayabe, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.
American Journal of Human Genetics|July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth diseaseDaniel G Calame, Tianyu Guo, Chen Wang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2012
The mammalian gene function resource: the International Knockout Mouse ConsortiumAllan Bradley, Konstantinos Anastassiadis, Abdelkader Ayadi, et al.
Nature|September 15, 2016
High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature Cardiovascular Research|April 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
Nature|November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Pageof 6