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

Michael Ludwig

Showing results (191-200 of 239) with videos related to

Pageof 24
Sort By:
European Journal of Medical Genetics|January 12, 2010
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophyMarkus Draaken, Heiko Reutter, Charlotte Schramm, et al.
Pediatric Nephrology (Berlin, Germany)|August 8, 2015
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencingStefanie Weber, Anja K Büscher, Henning Hagmann, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Zeitschrift Fur Gastroenterologie|February 26, 2026
[When Digital Meets Diagnostics: E-Learning Effectiveness in Internal Medicine Sonography Training]Johannes Weimer, Klaus Dirks, Michael Ludwig, et al.
Frontiers in Genetics|November 16, 2020
Impact of a <i>Gap Junction Protein Alpha 4</i> Variant on Clinical Disease Phenotype in <i>F508del</i> Homozygous Patients With Cystic FibrosisTabea Horn, Michael Ludwig, Olaf Eickmeier, et al.
European Journal of Pediatrics|November 3, 2010
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureCharlotte Schramm, Markus Draaken, Gabriel Tewes, et al.
Cancers|October 23, 2019
Mutational Landscape of the BAP1 Locus Reveals an Intrinsic Control to Regulate the miRNA Network and the Binding of Protein Complexes in Uveal MelanomaAmit Sharma, Arijit Biswas, Hongde Liu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
Schizophrenia Research|February 4, 2011
Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patientsThomas W Mühleisen, F Buket Basmanav, Andreas J Forstner, et al.
International Journal of Molecular Medicine|March 25, 2011
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complexLihong Qi, Kun Chen, David J Hur, et al.
Pageof 24

Showing results (191-200 of 239) with videos related to

Sort By:
Pageof 24
European Journal of Medical Genetics|January 12, 2010
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophyMarkus Draaken, Heiko Reutter, Charlotte Schramm, et al.
Pediatric Nephrology (Berlin, Germany)|August 8, 2015
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencingStefanie Weber, Anja K Büscher, Henning Hagmann, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Zeitschrift Fur Gastroenterologie|February 26, 2026
[When Digital Meets Diagnostics: E-Learning Effectiveness in Internal Medicine Sonography Training]Johannes Weimer, Klaus Dirks, Michael Ludwig, et al.
Frontiers in Genetics|November 16, 2020
Impact of a <i>Gap Junction Protein Alpha 4</i> Variant on Clinical Disease Phenotype in <i>F508del</i> Homozygous Patients With Cystic FibrosisTabea Horn, Michael Ludwig, Olaf Eickmeier, et al.
European Journal of Pediatrics|November 3, 2010
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureCharlotte Schramm, Markus Draaken, Gabriel Tewes, et al.
Cancers|October 23, 2019
Mutational Landscape of the BAP1 Locus Reveals an Intrinsic Control to Regulate the miRNA Network and the Binding of Protein Complexes in Uveal MelanomaAmit Sharma, Arijit Biswas, Hongde Liu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
Schizophrenia Research|February 4, 2011
Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patientsThomas W Mühleisen, F Buket Basmanav, Andreas J Forstner, et al.
International Journal of Molecular Medicine|March 25, 2011
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complexLihong Qi, Kun Chen, David J Hur, et al.
Pageof 24