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Human Genomics
|
September 18, 2010
KinSNP software for homozygosity mapping of disease genes using SNP microarrays
El-Ad David Amir, Ofer Bartal, Efrat Morad, et al.
The Journal of Physiology
|
October 22, 2015
Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 (-) secretion revealed by disease causing human mutation
Jeong Hee Hong, Emad Muhammad, Changyu Zheng, et al.
European Journal of Human Genetics : EJHG
|
October 1, 2015
D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias
Aviva Levitas, Yuval Konstantino, Emad Muhammad, et al.
Journal of the Neurological Sciences
|
December 9, 2008
Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy?
Yuval O Herishanu, Ruti Parvari, Yaakov Pollack, et al.
Biological Research
|
June 22, 2023
Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compaction
Nataly Korover, Sharon Etzion, Alexander Cherniak, et al.
International Journal of Molecular Sciences
|
May 13, 2023
Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred
Pierre Majdalani, Uri Yoel, Tayseer Nasasra, et al.
European Journal of Human Genetics : EJHG
|
June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase
Aviva Levitas, Emad Muhammad, Gali Harel, et al.
Scientific Reports
|
June 28, 2024
Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts
Sharon Etzion, Raneen Hijaze, Liad Segal, et al.
International Journal of Molecular Sciences
|
January 21, 2023
A Missense Variation in <i>PHACTR2</i> Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans
Pierre Majdalani, Aviva Levitas, Hanna Krymko, et al.
International Journal of Molecular Sciences
|
September 9, 2022
Dock10 Regulates Cardiac Function under Neurohormonal Stress
Liad Segal, Sharon Etzion, Sigal Elyagon, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Human Genomics
|
September 18, 2010
KinSNP software for homozygosity mapping of disease genes using SNP microarrays
El-Ad David Amir, Ofer Bartal, Efrat Morad, et al.
The Journal of Physiology
|
October 22, 2015
Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 (-) secretion revealed by disease causing human mutation
Jeong Hee Hong, Emad Muhammad, Changyu Zheng, et al.
European Journal of Human Genetics : EJHG
|
October 1, 2015
D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias
Aviva Levitas, Yuval Konstantino, Emad Muhammad, et al.
Journal of the Neurological Sciences
|
December 9, 2008
Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy?
Yuval O Herishanu, Ruti Parvari, Yaakov Pollack, et al.
Biological Research
|
June 22, 2023
Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compaction
Nataly Korover, Sharon Etzion, Alexander Cherniak, et al.
International Journal of Molecular Sciences
|
May 13, 2023
Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred
Pierre Majdalani, Uri Yoel, Tayseer Nasasra, et al.
European Journal of Human Genetics : EJHG
|
June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase
Aviva Levitas, Emad Muhammad, Gali Harel, et al.
Scientific Reports
|
June 28, 2024
Plekhm2 acts as an autophagy modulator in murine heart and cardiofibroblasts
Sharon Etzion, Raneen Hijaze, Liad Segal, et al.
International Journal of Molecular Sciences
|
January 21, 2023
A Missense Variation in <i>PHACTR2</i> Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans
Pierre Majdalani, Aviva Levitas, Hanna Krymko, et al.
International Journal of Molecular Sciences
|
September 9, 2022
Dock10 Regulates Cardiac Function under Neurohormonal Stress
Liad Segal, Sharon Etzion, Sigal Elyagon, et al.
Page
of 5