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

U Ludwig

Showing results (171-180 of 204) with videos related to

Pageof 21
Sort By:
Journal of Dental Research|August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome SequencingA K Hoebel, D Drichel, M van de Vorst, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
Frontiers in Genetics|August 4, 2022
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema GenesCarina M Mathey, Carlo Maj, Annika B Scheer, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
American Journal of Human Genetics|March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft PalateElisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Plos One|November 1, 2018
Exome sequencing in large, multiplex bipolar disorder families from CubaAnna Maaser, Andreas J Forstner, Jana Strohmaier, et al.
Journal of Dental Research|November 12, 2016
Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel SequencingK D Khandelwal, N Ishorst, H Zhou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 30, 2024
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distalI Claus, S Sivalingam, A C Koller, et al.
Immunity|October 19, 2017
Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer ImmunotherapyNicole Glodde, Tobias Bald, Debby van den Boorn-Konijnenberg, et al.
Science (New York, N.Y.)|January 13, 2021
Structure-guided multivalent nanobodies block SARS-CoV-2 infection and suppress mutational escapePaul-Albert Koenig, Hrishikesh Das, Hejun Liu, et al.
Pageof 21

Showing results (171-180 of 204) with videos related to

Sort By:
Pageof 21
Journal of Dental Research|August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome SequencingA K Hoebel, D Drichel, M van de Vorst, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
Frontiers in Genetics|August 4, 2022
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema GenesCarina M Mathey, Carlo Maj, Annika B Scheer, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
American Journal of Human Genetics|March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft PalateElisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Plos One|November 1, 2018
Exome sequencing in large, multiplex bipolar disorder families from CubaAnna Maaser, Andreas J Forstner, Jana Strohmaier, et al.
Journal of Dental Research|November 12, 2016
Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel SequencingK D Khandelwal, N Ishorst, H Zhou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 30, 2024
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distalI Claus, S Sivalingam, A C Koller, et al.
Immunity|October 19, 2017
Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer ImmunotherapyNicole Glodde, Tobias Bald, Debby van den Boorn-Konijnenberg, et al.
Science (New York, N.Y.)|January 13, 2021
Structure-guided multivalent nanobodies block SARS-CoV-2 infection and suppress mutational escapePaul-Albert Koenig, Hrishikesh Das, Hejun Liu, et al.
Pageof 21