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R Beeri

Showing results (11-20 of 21) with videos related to

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Current Biology : CB|September 1, 1995
Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in miceR Beeri, C Andres, E Lev-Lehman, et al.
The American Journal of Cardiology|September 15, 1996
Left ventricular free wall rupture as the presenting manifestation of acute myocardial infarction in diabetic patientsD Zahger, E Milgalter, A Pollak, et al.
Human Reproduction (Oxford, England)|February 1, 1994
Testicular amplification and impaired transmission of human butyrylcholinesterase cDNA in transgenic miceR Beeri, A Gnatt, Y Lapidot-Lifson, et al.
Journal of Neurochemistry|December 31, 1997
Enhanced hemicholinium binding and attenuated dendrite branching in cognitively impaired acetylcholinesterase-transgenic miceR Beeri, N Le Novère, R Mervis, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1997
Acetylcholinesterase-transgenic mice display embryonic modulations in spinal cord choline acetyltransferase and neurexin Ibeta gene expression followed by late-onset neuromotor deteriorationC Andres, R Beeri, A Friedman, et al.
Kidney International|June 1, 1995
Rapid DNA fragmentation from hypoxia along the thick ascending limb of rat kidneysR Beeri, Z Symon, M Brezis, et al.
The American Journal of Gastroenterology|November 1, 1992
Seasonal fluctuations in acute upper gastrointestinal bleeding: lack of effect of nonsteroidal anti-inflammatory drugsJ Zimmerman, R Arnon, R Beeri, et al.
Israel Journal of Medical Sciences|May 1, 1993
Acute upper gastrointestinal bleeding in Jerusalem 1988-91: causes, characteristics and relation to nonsteroidal anti-inflammatory drugsJ Zimmerman, R Arnon, M Ligumski, et al.
Oncogene|October 6, 2009
Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi originI Wolf, Y Laitman, T Rubinek, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Current Biology : CB|September 1, 1995
Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in miceR Beeri, C Andres, E Lev-Lehman, et al.
The American Journal of Cardiology|September 15, 1996
Left ventricular free wall rupture as the presenting manifestation of acute myocardial infarction in diabetic patientsD Zahger, E Milgalter, A Pollak, et al.
Human Reproduction (Oxford, England)|February 1, 1994
Testicular amplification and impaired transmission of human butyrylcholinesterase cDNA in transgenic miceR Beeri, A Gnatt, Y Lapidot-Lifson, et al.
Journal of Neurochemistry|December 31, 1997
Enhanced hemicholinium binding and attenuated dendrite branching in cognitively impaired acetylcholinesterase-transgenic miceR Beeri, N Le Novère, R Mervis, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1997
Acetylcholinesterase-transgenic mice display embryonic modulations in spinal cord choline acetyltransferase and neurexin Ibeta gene expression followed by late-onset neuromotor deteriorationC Andres, R Beeri, A Friedman, et al.
Kidney International|June 1, 1995
Rapid DNA fragmentation from hypoxia along the thick ascending limb of rat kidneysR Beeri, Z Symon, M Brezis, et al.
The American Journal of Gastroenterology|November 1, 1992
Seasonal fluctuations in acute upper gastrointestinal bleeding: lack of effect of nonsteroidal anti-inflammatory drugsJ Zimmerman, R Arnon, R Beeri, et al.
Israel Journal of Medical Sciences|May 1, 1993
Acute upper gastrointestinal bleeding in Jerusalem 1988-91: causes, characteristics and relation to nonsteroidal anti-inflammatory drugsJ Zimmerman, R Arnon, M Ligumski, et al.
Oncogene|October 6, 2009
Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi originI Wolf, Y Laitman, T Rubinek, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Pageof 3