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

Jochen Hecht

Showing results (61-70 of 87) with videos related to

Pageof 9
Sort By:
Human Molecular Genetics|February 26, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus modelThorsten Pfirrmann, Denise Emmerich, Peter Ruokonen, et al.
Kidney International|September 14, 2022
In vitro and in vivo evidence that the switch from calcineurin to mTOR inhibitors may be a strategy for immunosuppression in Epstein-Barr virus-associated post-transplant lymphoproliferative disorderConstantin J Thieme, Malissa Schulz, Patrizia Wehler, et al.
American Journal of Human Genetics|October 2, 2012
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locusMalte Spielmann, Francesco Brancati, Peter M Krawitz, et al.
Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.
Blood|April 23, 2013
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutationsMartin Neumann, Sandra Heesch, Cornelia Schlee, et al.
Communications Biology|June 9, 2023
Y chromosome sequence and epigenomic reconstruction across human populationsPaula Esteller-Cucala, Marc Palmada-Flores, Lukas F K Kuderna, et al.
American Journal of Human Genetics|December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosisEva Klopocki, Silke Lohan, Francesco Brancati, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Microbiome|December 8, 2018
Citizen science charts two major "stomatotypes" in the oral microbiome of adolescents and reveals links with habits and drinking water compositionJesse R Willis, Pedro González-Torres, Alexandros A Pittis, et al.
Science Translational Medicine|January 14, 2021
The intratumoral CXCR3 chemokine system is predictive of chemotherapy response in human bladder cancerTino Vollmer, Stephan Schlickeiser, Leila Amini, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|February 26, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus modelThorsten Pfirrmann, Denise Emmerich, Peter Ruokonen, et al.
Kidney International|September 14, 2022
In vitro and in vivo evidence that the switch from calcineurin to mTOR inhibitors may be a strategy for immunosuppression in Epstein-Barr virus-associated post-transplant lymphoproliferative disorderConstantin J Thieme, Malissa Schulz, Patrizia Wehler, et al.
American Journal of Human Genetics|October 2, 2012
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locusMalte Spielmann, Francesco Brancati, Peter M Krawitz, et al.
Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.
Blood|April 23, 2013
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutationsMartin Neumann, Sandra Heesch, Cornelia Schlee, et al.
Communications Biology|June 9, 2023
Y chromosome sequence and epigenomic reconstruction across human populationsPaula Esteller-Cucala, Marc Palmada-Flores, Lukas F K Kuderna, et al.
American Journal of Human Genetics|December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosisEva Klopocki, Silke Lohan, Francesco Brancati, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Microbiome|December 8, 2018
Citizen science charts two major "stomatotypes" in the oral microbiome of adolescents and reveals links with habits and drinking water compositionJesse R Willis, Pedro González-Torres, Alexandros A Pittis, et al.
Science Translational Medicine|January 14, 2021
The intratumoral CXCR3 chemokine system is predictive of chemotherapy response in human bladder cancerTino Vollmer, Stephan Schlickeiser, Leila Amini, et al.
Pageof 9