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

J Stephan

Showing results (121-130 of 130) with videos related to

Pageof 13
Sort By:
You have reached the last page of results.This site can display upto 130 results.
Journal of Psychiatric Practice|May 15, 2023
A New Treatment Program: Focused Integrated Team-based Treatment Program for Bipolar Disorder (FITT-BD)Louisa G Sylvia, Roberta E Tovey, Douglas Katz, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 7, 2022
Phase IIa Proof-of-Concept Evaluation of the Antiviral Efficacy, Safety, Tolerability, and Pharmacokinetics of the Next-Generation Maturation Inhibitor GSK3640254Christoph D Spinner, Franco Felizarta, Giuliano Rizzardini, et al.
Mbio|August 1, 2019
Dissecting the Gene Expression, Localization, Membrane Topology, and Function of the Plasmodium falciparum STEVOR Protein FamilyJ Stephan Wichers, Judith A M Scholz, Jan Strauss, et al.
Chest|February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|August 9, 2014
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophyKimberly A Aldinger, Stephen J Mosca, Martine Tétreault, et al.
Elife|April 28, 2021
Common virulence gene expression in adult first-time infected malaria patients and severe casesJ Stephan Wichers, Gerry Tonkin-Hill, Thorsten Thye, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Journal of Minimally Invasive Gynecology|April 18, 2026
Prospective multicentre registry study on sacropexy using the semitendinosus tendon for apical prolapse repair: an interim analysisDr Med C Schröder, Prof Dr Med A Hornemann, Dr Med V Engler, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Journal of Psychiatric Practice|May 15, 2023
A New Treatment Program: Focused Integrated Team-based Treatment Program for Bipolar Disorder (FITT-BD)Louisa G Sylvia, Roberta E Tovey, Douglas Katz, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 7, 2022
Phase IIa Proof-of-Concept Evaluation of the Antiviral Efficacy, Safety, Tolerability, and Pharmacokinetics of the Next-Generation Maturation Inhibitor GSK3640254Christoph D Spinner, Franco Felizarta, Giuliano Rizzardini, et al.
Mbio|August 1, 2019
Dissecting the Gene Expression, Localization, Membrane Topology, and Function of the Plasmodium falciparum STEVOR Protein FamilyJ Stephan Wichers, Judith A M Scholz, Jan Strauss, et al.
Chest|February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|August 9, 2014
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophyKimberly A Aldinger, Stephen J Mosca, Martine Tétreault, et al.
Elife|April 28, 2021
Common virulence gene expression in adult first-time infected malaria patients and severe casesJ Stephan Wichers, Gerry Tonkin-Hill, Thorsten Thye, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Journal of Minimally Invasive Gynecology|April 18, 2026
Prospective multicentre registry study on sacropexy using the semitendinosus tendon for apical prolapse repair: an interim analysisDr Med C Schröder, Prof Dr Med A Hornemann, Dr Med V Engler, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
Pageof 13