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Muralitharan Shanmugakonar
Muralitharan Shanmugakonar
Laboratory Manager, Laboratory Animal Research Centre, Qatar University
Verified email at qu.edu.qa
Title
Cited by
Cited by
Year
Tight junction proteins and signaling pathways in cancer and inflammation: a functional crosstalk
AA Bhat, S Uppada, IW Achkar, S Hashem, SK Yadav, M Shanmugakonar, ...
Frontiers in physiology 9, 1942, 2019
3412019
RAS-mediated oncogenic signaling pathways in human malignancies
AQ Khan, S Kuttikrishnan, KS Siveen, KS Prabhu, M Shanmugakonar, ...
Seminars in cancer biology 54, 1-13, 2019
1572019
Claudin-1, a double-edged sword in cancer
AA Bhat, N Syed, L Therachiyil, S Nisar, S Hashem, MA Macha, SK Yadav, ...
International journal of molecular sciences 21 (2), 569, 2020
992020
Absence of deafness‐associated connexin‐26 (GJB2) gene mutations in the Omani population
M Simsek, N Al‐Wardy, A Al‐Khayat, M Shanmugakonar, T Al‐Bulushi, ...
Human mutation 18 (6), 545-546, 2001
592001
Seminars in cancer biology
AQ Khan, S Kuttikrishnan, KS Siveen, KS Prabhu, M Shanmugakonar, ...
Elsevier, 2019
402019
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia
A Hempelmann, S Kumar, S Muralitharan, T Sander
Neuroscience letters 402 (1-2), 118-120, 2006
352006
Genotyping of the three major allelic variants of the human mannose‐binding lectin gene by denaturing gradient gel electrophoresis
M Gabolde, S Muralitharan, C Besmond
Human mutation 14 (1), 80-83, 1999
311999
Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients
S Muralitharan, YA Wali, D Dennison, ZA Lamki, M Zachariah, EB Nagwa, ...
American journal of hematology 82 (12), 1099-1102, 2007
252007
Exploring dysregulated signaling pathways in cancer
S Nisar, S Hashem, MA Macha, SK Yadav, S Muralitharan, L Therachiyil, ...
Current Pharmaceutical Design 26 (4), 429-445, 2020
232020
NF-κB Essential MOdulator (NEMO) Is Critical for Thyroid Function
Journal of Biological Chemistry, 2016
222016
Hereditary thrombophilia in ethnic Omani patients
A Pathare, S Al Kindi, H Al Haddabi, D Dennison, R Bayoumi, ...
American journal of hematology 81 (2), 101-106, 2006
222006
NF-kB Essential MOdulator (NEMO) Is Critical for Thyroid Function.
SR Reale C, Iervolino A, Scudiero I, Ferravante A, D'Andrea LE, Mazzone P ...
J Biol Chem. 2016 Jan 19., 0
22*
Hemoglobin disorders: Molecular methods and protocols
RL Nagel
Springer Science & Business Media, 2008
202008
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolate
J Turnbull, S Kumar, ZP Ren, S Muralitharan, T Naranian, CA Ackerley, ...
Journal of child neurology 23 (2), 240-242, 2008
202008
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemia
Z Al-Lamki, YA Wali, SM Wasifuddin, M Zachariah, R Al-Mjeni, C Li, ...
Pediatric hematology and oncology 22 (7), 629-643, 2005
202005
Allele-specific amplification of exon 7 in the survival motor neuron (SMN) genes for molecular diagnosis of spinal muscular atrophy.
M Simsek, T Al-Bulushi, M Shanmugakonar, HS Al-Barwani, R Bayoumi
Genetic Testing 7 (4), 325-327, 2003
182003
Chronic cadmium exposure alters cardiac matrix metalloproteinases in the heart of Sprague-Dawley rat
SC Das, K Varadharajan, M Shanmugakonar, HA Al-Naemi
Frontiers in Pharmacology 12, 663048, 2021
162021
β-globin-like gene cluster haplotypes in hemoglobinopathies
S Muralitharan, R Krishnamoorthy, RL Nagel
Hemoglobin Disorders: Molecular Methods and Protocols, 195-211, 2003
162003
β-globin-like gene cluster haplotypes in hemoglobinopathies
S Muralitharan, R Krishnamoorthy, RL Nagel
Hemoglobin Disorders: Molecular Methods and Protocols, 195-211, 2003
162003
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression
S Muralitharan, Z Al Lamki, D Dennison, BS Christie, YA Wali, ...
American journal of hematology 78 (1), 59-63, 2005
152005
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