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Marcus Dittrich

Showing results (41-50 of 89) with videos related to

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Molecular Genetics & Genomic Medicine|June 11, 2020
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German familyJulia Doll, Michaela A H Hofrichter, Paulina Bahena, et al.
Aging|February 27, 2023
Age-related methylation changes in the human sperm epigenomeLaura Bernhardt, Marcus Dittrich, Andreas Prell, et al.
Plant Physiology|September 21, 2012
Poplar wood rays are involved in seasonal remodeling of tree physiologyChristina Larisch, Marcus Dittrich, Henning Wildhagen, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|July 14, 2022
Treatment Algorithm for Patients With von Willebrand Syndrome Type 2A and Congenital Heart Disease-A Treatment Algorithm May Reduce Perioperative Blood Loss in Children With Congenital Heart DiseaseJulian Wolf, Christina Brandenburger, Marcus Dittrich, et al.
Aging|November 29, 2023
Effects of paternal and chronological age on <i>BEGAIN</i> methylation and its possible role in autismRamya Potabattula, Andreas Prell, Marcus Dittrich, et al.
Diabetes|December 5, 2012
Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitusNady El Hajj, Galyna Pliushch, Eberhard Schneider, et al.
Plant Physiology|May 11, 2012
Poplar extrafloral nectaries: two types, two strategies of indirect defenses against herbivoresMaría Escalante-Pérez, Mario Jaborsky, Silke Lautner, et al.
Gene|July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain developmentEberhard Schneider, Marcus Dittrich, Julia Böck, et al.
Transplantation|March 3, 2021
Graft-derived Cell-free DNA as a Noninvasive Biomarker of Cardiac Allograft Rejection: A Cohort Study on Clinical Validity and Confounding FactorsFranziska Knüttgen, Julia Beck, Marcus Dittrich, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Molecular Genetics & Genomic Medicine|June 11, 2020
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German familyJulia Doll, Michaela A H Hofrichter, Paulina Bahena, et al.
Aging|February 27, 2023
Age-related methylation changes in the human sperm epigenomeLaura Bernhardt, Marcus Dittrich, Andreas Prell, et al.
Plant Physiology|September 21, 2012
Poplar wood rays are involved in seasonal remodeling of tree physiologyChristina Larisch, Marcus Dittrich, Henning Wildhagen, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|July 14, 2022
Treatment Algorithm for Patients With von Willebrand Syndrome Type 2A and Congenital Heart Disease-A Treatment Algorithm May Reduce Perioperative Blood Loss in Children With Congenital Heart DiseaseJulian Wolf, Christina Brandenburger, Marcus Dittrich, et al.
Aging|November 29, 2023
Effects of paternal and chronological age on <i>BEGAIN</i> methylation and its possible role in autismRamya Potabattula, Andreas Prell, Marcus Dittrich, et al.
Diabetes|December 5, 2012
Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitusNady El Hajj, Galyna Pliushch, Eberhard Schneider, et al.
Plant Physiology|May 11, 2012
Poplar extrafloral nectaries: two types, two strategies of indirect defenses against herbivoresMaría Escalante-Pérez, Mario Jaborsky, Silke Lautner, et al.
Gene|July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain developmentEberhard Schneider, Marcus Dittrich, Julia Böck, et al.
Transplantation|March 3, 2021
Graft-derived Cell-free DNA as a Noninvasive Biomarker of Cardiac Allograft Rejection: A Cohort Study on Clinical Validity and Confounding FactorsFranziska Knüttgen, Julia Beck, Marcus Dittrich, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Pageof 9