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Haloom Rafehi

Showing results (21-30 of 44) with videos related to

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Circulation|July 23, 2017
Multicellular Transcriptional Analysis of Mammalian Heart RegenerationGregory A Quaife-Ryan, Choon Boon Sim, Mark Ziemann, et al.
JCI Insight|March 30, 2017
<i>NET</i> silencing by <i>let-7i</i> in postural tachycardia syndromeAbdul Waheed Khan, Mark Ziemann, Susan J Corcoran, et al.
NPJ Parkinson'S Disease|November 14, 2024
Peripheral immune cell abundance differences link blood mitochondrial DNA copy number and Parkinson's diseaseLongfei Wang, Jiru Han, Liam G Fearnley, et al.
Pathobiology of Aging & Age Related Diseases|September 7, 2012
Investigation of the biological properties of Cinnulin PF in the context of diabetes: mechanistic insights by genome-wide mRNA-Seq analysisHaloom Rafehi, Katherine Ververis, Aneta Balcerczyk, et al.
Cellular and Molecular Life Sciences : CMLS|August 14, 2023
Characterization of K562 cells: uncovering novel chromosomes, assessing transferrin receptor expression, and probing pharmacological therapiesTom C Karagiannis, Meaghan Wall, Katherine Ververis, et al.
Food & Function|June 27, 2015
RNA sequencing supports distinct reactive oxygen species-mediated pathways of apoptosis by high and low size mass fractions of Bay leaf (Lauris nobilis) in HT-29 cellsAnnabelle L Rodd, Katherine Ververis, Dheeshana Sayakkarage, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 3, 2018
Galectin-3 deficiency ameliorates fibrosis and remodeling in dilated cardiomyopathy mice with enhanced Mst1 signalingMy-Nhan Nguyen, Mark Ziemann, Helen Kiriazis, et al.
Genome Research|April 16, 2014
Vascular histone deacetylation by pharmacological HDAC inhibitionHaloom Rafehi, Aneta Balcerczyk, Sebastian Lunke, et al.
European Journal of Human Genetics : EJHG|March 24, 2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian familiesMark F Bennett, Karen L Oliver, Brigid M Regan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Circulation|July 23, 2017
Multicellular Transcriptional Analysis of Mammalian Heart RegenerationGregory A Quaife-Ryan, Choon Boon Sim, Mark Ziemann, et al.
JCI Insight|March 30, 2017
<i>NET</i> silencing by <i>let-7i</i> in postural tachycardia syndromeAbdul Waheed Khan, Mark Ziemann, Susan J Corcoran, et al.
NPJ Parkinson'S Disease|November 14, 2024
Peripheral immune cell abundance differences link blood mitochondrial DNA copy number and Parkinson's diseaseLongfei Wang, Jiru Han, Liam G Fearnley, et al.
Pathobiology of Aging & Age Related Diseases|September 7, 2012
Investigation of the biological properties of Cinnulin PF in the context of diabetes: mechanistic insights by genome-wide mRNA-Seq analysisHaloom Rafehi, Katherine Ververis, Aneta Balcerczyk, et al.
Cellular and Molecular Life Sciences : CMLS|August 14, 2023
Characterization of K562 cells: uncovering novel chromosomes, assessing transferrin receptor expression, and probing pharmacological therapiesTom C Karagiannis, Meaghan Wall, Katherine Ververis, et al.
Food & Function|June 27, 2015
RNA sequencing supports distinct reactive oxygen species-mediated pathways of apoptosis by high and low size mass fractions of Bay leaf (Lauris nobilis) in HT-29 cellsAnnabelle L Rodd, Katherine Ververis, Dheeshana Sayakkarage, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 3, 2018
Galectin-3 deficiency ameliorates fibrosis and remodeling in dilated cardiomyopathy mice with enhanced Mst1 signalingMy-Nhan Nguyen, Mark Ziemann, Helen Kiriazis, et al.
Genome Research|April 16, 2014
Vascular histone deacetylation by pharmacological HDAC inhibitionHaloom Rafehi, Aneta Balcerczyk, Sebastian Lunke, et al.
European Journal of Human Genetics : EJHG|March 24, 2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian familiesMark F Bennett, Karen L Oliver, Brigid M Regan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Pageof 5