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Shanmugakonar Muralitharan

Showing results (1-10 of 9) with videos related to

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Neuroscience Letters|April 25, 2006
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesiaAnne Hempelmann, Santosh Kumar, Shanmugakonar Muralitharan, et al.
Journal of Child Neurology|February 12, 2008
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolateJulie Turnbull, Santosh Kumar, Zhi-Ping Ren, et al.
Journal of Child Neurology|October 18, 2007
Clinical and genetic study of spinal muscular atrophies in OmanRoshan Koul, Amna Al Futaisi, Alexander Chacko, et al.
Neurosciences (Riyadh, Saudi Arabia)|April 5, 2012
Trinucleotide repeat analysis of spinocerebellar ataxia patients in OmanJacob P Chacko, Shanmugakonar Muralitharan, Alia Al-Ansari, et al.
American Journal of Hematology|August 4, 2007
Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patientsShanmugakonar Muralitharan, Yasser A Wali, David Dennison, et al.
American Journal of Hematology|December 21, 2004
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expressionShanmugakonar Muralitharan, Zakia Al Lamki, David Dennison, et al.
Cell Death & Disease|February 24, 2017
CARMA2sh and ULK2 control pathogen-associated molecular patterns recognition in human keratinocytes: psoriasis-linked CARMA2sh mutants escape ULK2 censorshipIvan Scudiero, Pellegrino Mazzone, Luca E D'Andrea, et al.
Pediatric Hematology and Oncology|September 17, 2005
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemiaZakia Al-Lamki, Yasser A Wali, Shah M Wasifuddin, et al.
International Journal of Molecular Sciences|January 19, 2020
Claudin-1, A Double-Edged Sword in CancerAjaz A Bhat, Najeeb Syed, Lubna Therachiyil, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Neuroscience Letters|April 25, 2006
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesiaAnne Hempelmann, Santosh Kumar, Shanmugakonar Muralitharan, et al.
Journal of Child Neurology|February 12, 2008
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolateJulie Turnbull, Santosh Kumar, Zhi-Ping Ren, et al.
Journal of Child Neurology|October 18, 2007
Clinical and genetic study of spinal muscular atrophies in OmanRoshan Koul, Amna Al Futaisi, Alexander Chacko, et al.
Neurosciences (Riyadh, Saudi Arabia)|April 5, 2012
Trinucleotide repeat analysis of spinocerebellar ataxia patients in OmanJacob P Chacko, Shanmugakonar Muralitharan, Alia Al-Ansari, et al.
American Journal of Hematology|August 4, 2007
Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patientsShanmugakonar Muralitharan, Yasser A Wali, David Dennison, et al.
American Journal of Hematology|December 21, 2004
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expressionShanmugakonar Muralitharan, Zakia Al Lamki, David Dennison, et al.
Cell Death & Disease|February 24, 2017
CARMA2sh and ULK2 control pathogen-associated molecular patterns recognition in human keratinocytes: psoriasis-linked CARMA2sh mutants escape ULK2 censorshipIvan Scudiero, Pellegrino Mazzone, Luca E D'Andrea, et al.
Pediatric Hematology and Oncology|September 17, 2005
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemiaZakia Al-Lamki, Yasser A Wali, Shah M Wasifuddin, et al.
International Journal of Molecular Sciences|January 19, 2020
Claudin-1, A Double-Edged Sword in CancerAjaz A Bhat, Najeeb Syed, Lubna Therachiyil, et al.
Pageof 1