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Martin Zenker

Showing results (131-140 of 338) with videos related to

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Molecular Genetics and Metabolism|April 16, 2008
Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson-Mendenhall syndromeChristian T Thiel, Birgit Knebel, Ina Knerr, et al.
Respiratory Research|August 8, 2006
Magnetic resonance lung function--a breakthrough for lung imaging and functional assessment? A phantom study and clinical trialMaren Zapke, Hans-Georg Topf, Martin Zenker, et al.
Blood|January 30, 2010
Mutational analysis of SHOC2, a novel gene for Noonan-like syndrome, in JMMLChristian Flotho, Christiane Batz, Henrik Hasle, et al.
Cell Communication and Signaling : CCS|December 7, 2018
bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signalingFereshteh Haghighi, Julia Dahlmann, Saeideh Nakhaei-Rad, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndromeMartin Zenker, Tim Tralau, Thomas Lennert, et al.
Computer Methods in Biomechanics and Biomedical Engineering|July 14, 2022
Quantifying osteosynthesis plate prominence - mathematical definitions and case study on a clavicle plateMartin Zenker, Evangelos Theodorou, Daniel Andermatt, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 15, 2018
Genetic basis of hypertrophic cardiomyopathy in childrenStefan Rupp, Moataz Felimban, Anne Schänzer, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|October 4, 2013
Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish typeSonbol Ameli, Martin Zenker, Ameneh Zare-Shahabadi, et al.
American Journal of Respiratory and Critical Care Medicine|February 20, 2024
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway MalformationsJonas Windrich, Peter Braubach, Florian Länger, et al.
Trials|June 6, 2023
Improvement of synaptic plasticity and cognitive function in RASopathies-a monocentre, randomized, double-blind, parallel-group, placebo-controlled, cross-over clinical trial (SynCoRAS)Nikolai H Jung, Silvia Egert-Schwender, Beate Schossow, et al.
Pageof 34

Showing results (131-140 of 338) with videos related to

Sort By:
Pageof 34
Molecular Genetics and Metabolism|April 16, 2008
Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson-Mendenhall syndromeChristian T Thiel, Birgit Knebel, Ina Knerr, et al.
Respiratory Research|August 8, 2006
Magnetic resonance lung function--a breakthrough for lung imaging and functional assessment? A phantom study and clinical trialMaren Zapke, Hans-Georg Topf, Martin Zenker, et al.
Blood|January 30, 2010
Mutational analysis of SHOC2, a novel gene for Noonan-like syndrome, in JMMLChristian Flotho, Christiane Batz, Henrik Hasle, et al.
Cell Communication and Signaling : CCS|December 7, 2018
bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signalingFereshteh Haghighi, Julia Dahlmann, Saeideh Nakhaei-Rad, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndromeMartin Zenker, Tim Tralau, Thomas Lennert, et al.
Computer Methods in Biomechanics and Biomedical Engineering|July 14, 2022
Quantifying osteosynthesis plate prominence - mathematical definitions and case study on a clavicle plateMartin Zenker, Evangelos Theodorou, Daniel Andermatt, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 15, 2018
Genetic basis of hypertrophic cardiomyopathy in childrenStefan Rupp, Moataz Felimban, Anne Schänzer, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|October 4, 2013
Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish typeSonbol Ameli, Martin Zenker, Ameneh Zare-Shahabadi, et al.
American Journal of Respiratory and Critical Care Medicine|February 20, 2024
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway MalformationsJonas Windrich, Peter Braubach, Florian Länger, et al.
Trials|June 6, 2023
Improvement of synaptic plasticity and cognitive function in RASopathies-a monocentre, randomized, double-blind, parallel-group, placebo-controlled, cross-over clinical trial (SynCoRAS)Nikolai H Jung, Silvia Egert-Schwender, Beate Schossow, et al.
Pageof 34