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Thomas Meitinger

Showing results (71-80 of 536) with videos related to

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Seizure|March 7, 2021
Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1BMartin Krenn, Monika Schloegl, Ekaterina Pataraia, et al.
Stroke|February 3, 2009
Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populationsTobias Freilinger, Steve Bevan, Stephan Ripke, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9Katharina Danhauser, Diran Herebian, Tobias B Haack, et al.
British Journal of Pharmacology|November 28, 2020
Stimulation of soluble guanylyl cyclase (sGC) by riociguat attenuates heart failure and pathological cardiac remodellingJulia Rüdebusch, Alexander Benkner, Neetika Nath, et al.
Stem Cell Research|November 24, 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 geneXianming Wang, Shen Chen, Ingo Burtscher, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15Ingrid Bader, Oliver Brandau, Helene Achatz, et al.
Circulation|February 8, 2021
MicroRNA-21-Dependent Macrophage-to-Fibroblast Signaling Determines the Cardiac Response to Pressure OverloadDeepak Ramanujam, Anna Patricia Schön, Christina Beck, et al.
Clinical Genetics|April 5, 2019
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limbMuhammad Umair, Muhammad Bilal, Raja H Ali, et al.
Stem Cell Research|November 24, 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 geneXianming Wang, Shen Chen, Ingo Burtscher, et al.
Biological Psychiatry|February 13, 2010
CLOCK gene variants associate with sleep duration in two independent populationsKarla V Allebrandt, Maris Teder-Laving, Mahmut Akyol, et al.
Pageof 54

Showing results (71-80 of 536) with videos related to

Sort By:
Pageof 54
Seizure|March 7, 2021
Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1BMartin Krenn, Monika Schloegl, Ekaterina Pataraia, et al.
Stroke|February 3, 2009
Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populationsTobias Freilinger, Steve Bevan, Stephan Ripke, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9Katharina Danhauser, Diran Herebian, Tobias B Haack, et al.
British Journal of Pharmacology|November 28, 2020
Stimulation of soluble guanylyl cyclase (sGC) by riociguat attenuates heart failure and pathological cardiac remodellingJulia Rüdebusch, Alexander Benkner, Neetika Nath, et al.
Stem Cell Research|November 24, 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 geneXianming Wang, Shen Chen, Ingo Burtscher, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15Ingrid Bader, Oliver Brandau, Helene Achatz, et al.
Circulation|February 8, 2021
MicroRNA-21-Dependent Macrophage-to-Fibroblast Signaling Determines the Cardiac Response to Pressure OverloadDeepak Ramanujam, Anna Patricia Schön, Christina Beck, et al.
Clinical Genetics|April 5, 2019
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limbMuhammad Umair, Muhammad Bilal, Raja H Ali, et al.
Stem Cell Research|November 24, 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 geneXianming Wang, Shen Chen, Ingo Burtscher, et al.
Biological Psychiatry|February 13, 2010
CLOCK gene variants associate with sleep duration in two independent populationsKarla V Allebrandt, Maris Teder-Laving, Mahmut Akyol, et al.
Pageof 54