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Y Birnbaum

Showing results (121-130 of 153) with videos related to

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Journal of Medical Genetics|November 8, 2015
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCNYonatan Perez, Rotem Kadir, Michael Volodarsky, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesisShai Adar-Levor, Dikla Nachmias, Shani T Gal-Oz, et al.
Circulation|January 28, 1998
Noninvasive in vivo clot dissolution without a thrombolytic drug: recanalization of thrombosed iliofemoral arteries by transcutaneous ultrasound combined with intravenous infusion of microbubblesY Birnbaum, H Luo, T Nagai, et al.
BMC Medical Genetics|December 22, 2011
Association analysis identifies ZNF750 regulatory variants in psoriasisRamon Y Birnbaum, Genki Hayashi, Idan Cohen, et al.
Journal of the American College of Cardiology|February 17, 2000
Persistent ST segment depression in precordial leads V5-V6 after Q-wave anterior wall myocardial infarction is associated with restrictive physiology of the left ventricleA Assali, S Sclarovsky, I Herz, et al.
American Heart Journal|May 29, 2001
Prediction of the extent and severity of left ventricular dysfunction in anterior acute myocardial infarction by the admission electrocardiogramY Birnbaum, D A Criger, G S Wagner, et al.
Translational Psychiatry|September 3, 2014
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genesN Oksenberg, G D E Haliburton, W L Eckalbar, et al.
Plos Genetics|October 30, 2018
Unraveling the transcriptional regulation of TWIST1 in limb developmentNaama Hirsch, Reut Eshel, Reut Bar Yaacov, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
The American Journal of Cardiology|August 15, 1996
Distortion of the terminal portion of the QRS on the admission electrocardiogram in acute myocardial infarction and correlation with infarct size and long-term prognosis (Thrombolysis in Myocardial Infarction 4 Trial)Y Birnbaum, R A Kloner, S Sclarovsky, et al.
Pageof 16

Showing results (121-130 of 153) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|November 8, 2015
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCNYonatan Perez, Rotem Kadir, Michael Volodarsky, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesisShai Adar-Levor, Dikla Nachmias, Shani T Gal-Oz, et al.
Circulation|January 28, 1998
Noninvasive in vivo clot dissolution without a thrombolytic drug: recanalization of thrombosed iliofemoral arteries by transcutaneous ultrasound combined with intravenous infusion of microbubblesY Birnbaum, H Luo, T Nagai, et al.
BMC Medical Genetics|December 22, 2011
Association analysis identifies ZNF750 regulatory variants in psoriasisRamon Y Birnbaum, Genki Hayashi, Idan Cohen, et al.
Journal of the American College of Cardiology|February 17, 2000
Persistent ST segment depression in precordial leads V5-V6 after Q-wave anterior wall myocardial infarction is associated with restrictive physiology of the left ventricleA Assali, S Sclarovsky, I Herz, et al.
American Heart Journal|May 29, 2001
Prediction of the extent and severity of left ventricular dysfunction in anterior acute myocardial infarction by the admission electrocardiogramY Birnbaum, D A Criger, G S Wagner, et al.
Translational Psychiatry|September 3, 2014
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genesN Oksenberg, G D E Haliburton, W L Eckalbar, et al.
Plos Genetics|October 30, 2018
Unraveling the transcriptional regulation of TWIST1 in limb developmentNaama Hirsch, Reut Eshel, Reut Bar Yaacov, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
The American Journal of Cardiology|August 15, 1996
Distortion of the terminal portion of the QRS on the admission electrocardiogram in acute myocardial infarction and correlation with infarct size and long-term prognosis (Thrombolysis in Myocardial Infarction 4 Trial)Y Birnbaum, R A Kloner, S Sclarovsky, et al.
Pageof 16