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M Memmi

Showing results (11-20 of 19) with videos related to

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The Journal of Biological Chemistry|June 19, 2001
Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypesI Rivolta, H Abriel, M Tateyama, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 22, 2000
Mechanisms of I(Ks) suppression in LQT1 mutantsL Bianchi, S G Priori, C Napolitano, et al.
Circulation Research|April 17, 2001
Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channelH Abriel, C Cabo, X H Wehrens, et al.
Oncogene|October 23, 2012
The Cul4A-DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activityM Malatesta, A Peschiaroli, E M Memmi, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndromeE Ficker, D Thomas, P C Viswanathan, et al.
Human Immunology|September 7, 2001
Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the regionR Scozzari, F Cruciani, A Pangrazio, et al.
American Journal of Physical Anthropology|May 29, 2003
Peopling of three Mediterranean islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variabilityP Francalacci, L Morelli, P A Underhill, et al.
Leukemia|December 7, 2017
The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemiaA G Sanarico, C Ronchini, A Croce, et al.
Annals of Human Genetics|April 3, 2001
Patterns of male-specific inter-population divergence in Europe, West Asia and North AfricaP Malaspina, F Cruciani, P Santolamazza, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
The Journal of Biological Chemistry|June 19, 2001
Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypesI Rivolta, H Abriel, M Tateyama, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 22, 2000
Mechanisms of I(Ks) suppression in LQT1 mutantsL Bianchi, S G Priori, C Napolitano, et al.
Circulation Research|April 17, 2001
Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channelH Abriel, C Cabo, X H Wehrens, et al.
Oncogene|October 23, 2012
The Cul4A-DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activityM Malatesta, A Peschiaroli, E M Memmi, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndromeE Ficker, D Thomas, P C Viswanathan, et al.
Human Immunology|September 7, 2001
Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the regionR Scozzari, F Cruciani, A Pangrazio, et al.
American Journal of Physical Anthropology|May 29, 2003
Peopling of three Mediterranean islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variabilityP Francalacci, L Morelli, P A Underhill, et al.
Leukemia|December 7, 2017
The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemiaA G Sanarico, C Ronchini, A Croce, et al.
Annals of Human Genetics|April 3, 2001
Patterns of male-specific inter-population divergence in Europe, West Asia and North AfricaP Malaspina, F Cruciani, P Santolamazza, et al.
Pageof 2