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Martin Zenker

Showing results (181-190 of 338) with videos related to

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Nature Communications|September 23, 2023
Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthoodKatrin Vogel, Aditya Arra, Holger Lingel, et al.
Molecular Syndromology|March 22, 2016
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II ErrorsRon Hochstenbach, Beata Nowakowska, Marianne Volleth, et al.
Ebiomedicine|May 1, 2022
Gut microbial similarity in twins is driven by shared environment and agingRamiro Vilchez-Vargas, Jurgita Skieceviciene, Konrad Lehr, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 16, 2019
Variants in nuclear factor I genes influence growth and developmentMartin Zenker, Jens Bunt, Ina Schanze, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|September 28, 2012
NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndromeSonbol Ameli, Mojgan Mazaheri, Ameneh Zare-Shahabadi, et al.
Orphanet Journal of Rare Diseases|June 10, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)Thomas Eggermann, Miriam Elbracht, Ingo Kurth, et al.
Cardiovascular Diagnosis and Therapy|November 19, 2019
Long-term outcomes of childhood onset Noonan compared to sarcomere hypertrophic cardiomyopathyEmanuel Kaltenecker, Julia Schleihauf, Christian Meierhofer, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 25, 2013
Inactivation of HNSCC cells by 90Y-labeled cetuximab strictly depends on the number of induced DNA double-strand breaksJarob Saker, Malte Kriegs, Martin Zenker, et al.
Nature Medicine|January 9, 2019
Identifying facial phenotypes of genetic disorders using deep learningYaron Gurovich, Yair Hanani, Omri Bar, et al.
Frontiers in Systems Neuroscience|August 23, 2014
Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expressionAnni Richter, Marc Guitart-Masip, Adriana Barman, et al.
Pageof 34

Showing results (181-190 of 338) with videos related to

Sort By:
Pageof 34
Nature Communications|September 23, 2023
Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthoodKatrin Vogel, Aditya Arra, Holger Lingel, et al.
Molecular Syndromology|March 22, 2016
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II ErrorsRon Hochstenbach, Beata Nowakowska, Marianne Volleth, et al.
Ebiomedicine|May 1, 2022
Gut microbial similarity in twins is driven by shared environment and agingRamiro Vilchez-Vargas, Jurgita Skieceviciene, Konrad Lehr, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 16, 2019
Variants in nuclear factor I genes influence growth and developmentMartin Zenker, Jens Bunt, Ina Schanze, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|September 28, 2012
NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndromeSonbol Ameli, Mojgan Mazaheri, Ameneh Zare-Shahabadi, et al.
Orphanet Journal of Rare Diseases|June 10, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)Thomas Eggermann, Miriam Elbracht, Ingo Kurth, et al.
Cardiovascular Diagnosis and Therapy|November 19, 2019
Long-term outcomes of childhood onset Noonan compared to sarcomere hypertrophic cardiomyopathyEmanuel Kaltenecker, Julia Schleihauf, Christian Meierhofer, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 25, 2013
Inactivation of HNSCC cells by 90Y-labeled cetuximab strictly depends on the number of induced DNA double-strand breaksJarob Saker, Malte Kriegs, Martin Zenker, et al.
Nature Medicine|January 9, 2019
Identifying facial phenotypes of genetic disorders using deep learningYaron Gurovich, Yair Hanani, Omri Bar, et al.
Frontiers in Systems Neuroscience|August 23, 2014
Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expressionAnni Richter, Marc Guitart-Masip, Adriana Barman, et al.
Pageof 34