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

Marcus Dittrich

Showing results (81-90 of 89) with videos related to

Pageof 9
Sort By:
You have reached the last page of results.This site can display upto 89 results.
International Journal of Medical Microbiology : IJMM|December 16, 2014
Modelling antibiotic and cytotoxic isoquinoline effects in Staphylococcus aureus, Staphylococcus epidermidis and mammalian cellsAlexander Cecil, Knut Ohlsen, Thomas Menzel, et al.
Science Translational Medicine|February 19, 2016
Long noncoding RNA Chast promotes cardiac remodelingJanika Viereck, Regalla Kumarswamy, Ariana Foinquinos, et al.
European Journal of Immunology|July 28, 2023
Enolase 1 of Candida albicans binds human CD4<sup>+</sup> T cells and modulates naïve and memory responsesMuhammad Daud, Prasad Dasari, Marion Adelfinger, et al.
Clinical Epigenetics|December 18, 2019
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulationLarissa Haertle, Tobias Müller, Roy Lardenoije, et al.
Nature Genetics|November 20, 2019
Chromatin establishes an immature version of neuronal protocadherin selection during the naive-to-primed conversion of pluripotent stem cellsAngels Almenar-Queralt, Daria Merkurjev, Hong Sook Kim, et al.
Genes|November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani FamiliesJulia Doll, Barbara Vona, Linda Schnapp, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2016
Natural mutations in a Staphylococcus aureus virulence regulator attenuate cytotoxicity but permit bacteremia and abscess formationSudip Das, Claudia Lindemann, Bernadette C Young, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossDaniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
International Journal of Medical Microbiology : IJMM|December 16, 2014
Modelling antibiotic and cytotoxic isoquinoline effects in Staphylococcus aureus, Staphylococcus epidermidis and mammalian cellsAlexander Cecil, Knut Ohlsen, Thomas Menzel, et al.
Science Translational Medicine|February 19, 2016
Long noncoding RNA Chast promotes cardiac remodelingJanika Viereck, Regalla Kumarswamy, Ariana Foinquinos, et al.
European Journal of Immunology|July 28, 2023
Enolase 1 of Candida albicans binds human CD4<sup>+</sup> T cells and modulates naïve and memory responsesMuhammad Daud, Prasad Dasari, Marion Adelfinger, et al.
Clinical Epigenetics|December 18, 2019
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulationLarissa Haertle, Tobias Müller, Roy Lardenoije, et al.
Nature Genetics|November 20, 2019
Chromatin establishes an immature version of neuronal protocadherin selection during the naive-to-primed conversion of pluripotent stem cellsAngels Almenar-Queralt, Daria Merkurjev, Hong Sook Kim, et al.
Genes|November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani FamiliesJulia Doll, Barbara Vona, Linda Schnapp, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2016
Natural mutations in a Staphylococcus aureus virulence regulator attenuate cytotoxicity but permit bacteremia and abscess formationSudip Das, Claudia Lindemann, Bernadette C Young, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossDaniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Pageof 9