Works matching AU Muralitharan, Shanmugakonar

Results: 13

Absence of deafness-associated connexin-26 ( GJB2) gene mutations in the Omani population.

Published in:

Human Mutation, 2001, v. 18, n. 6, p. 545, doi. 10.1002/humu.1233

By:

Simsek, Mehmet;
Al-Wardy, Nadia;
Al-Khayat, Aisha;
Shanmugakonar, Muralitharan;
Al-Bulushi, Talal;
Al-Khabory, Mazin;
Al-Mujeni, Sheikha;
Al-Harthi, Samia

Publication type:

Article

IDENTIFICATION OF PROGNOSIS MARKERS IN PEDIATRIC HIGH-RISK ACUTE LYMPHOBLASTIC LEUKEMIA.

Published in:

Pediatric Hematology & Oncology, 2005, v. 22, n. 7, p. 629, doi. 10.1080/08880010500199069

By:

Al-Lamki, Zakia;
Wali, Yasser A.;
Wasifuddin, Shah M.;
Zachariah, Mathew;
Al-Mjeni, Rayhanah;
Li, Changping;
Muralitharan, Shanmugakonar;
Al-Kharusi, Khalsa;
Gunaratne, Preethi;
Peterson, Leif;
Gibbs, Richard;
Gingras, Marie-Claude;
Margolin, Judith F.

Publication type:

Article

Tight Junction Proteins and Signaling Pathways in Cancer and Inflammation: A Functional Crosstalk.

Published in:

Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2018.01942

By:

Bhat, Ajaz A.;
Uppada, Srijayaprakash;
Achkar, Iman W.;
Hashem, Sheema;
Yadav, Santosh K.;
Shanmugakonar, Muralitharan;
Al-Naemi, Hamda A.;
Haris, Mohammad;
Uddin, Shahab

Publication type:

Article

Chronic Cadmium Exposure Alters Cardiac Matrix Metalloproteinases in the Heart of Sprague-Dawley Rat.

Published in:

Frontiers in Pharmacology, 2021, v. 12, p. 1, doi. 10.3389/fphar.2021.663048

By:

Das, Sandra Concepcion;
Varadharajan, Kavitha;
Shanmugakonar, Muralitharan;
Al-Naemi, Hamda A.

Publication type:

Article

Lafora Progressive Myoclonus Epilepsy: Disease Course Homogeneity in a Genetic Isolate.

Published in:

Journal of Child Neurology, 2008, v. 23, n. 2, p. 240, doi. 10.1177/0883073807309245

By:

Turnbull, Julie;
Kumar, Santosh;
Zhi-Ping Ren;
Muralitharan, Shanmugakonar;
Naranian, Taline;
Ackerley, Cameron A.;
Minassian, Berge A.

Publication type:

Article

Clinical and Genetic Study of Spinal Muscular Atrophies in Oman.

Published in:

Journal of Child Neurology, 2007, v. 22, n. 10, p. 1227, doi. 10.1177/0883073807306268

By:

Koul, Roshan;
Futaisi, Amna Al;
Chacko, Alexander;
Rao, Vasudev;
Simsek, Mehmet;
Muralitharan, Shanmugakonar;
Ganguly, Shyarn S.;
Bayourni, Riad

Publication type:

Article

Early‐Life Sugar Consumption Affects the Microbiome in Juvenile Mice.

Published in:

Molecular Nutrition & Food Research, 2023, v. 67, n. 24, p. 1, doi. 10.1002/mnfr.202200322

By:

Alasmar, Reem Moath;
Varadharajan, Kavitha;
Shanmugakonar, Muralitharan;
Al‐Naemi, Hamda A.

Publication type:

Article

Claudin-1, A Double-Edged Sword in Cancer.

Published in:

2020

By:

Bhat, Ajaz A.;
Syed, Najeeb;
Therachiyil, Lubna;
Nisar, Sabah;
Hashem, Sheema;
Macha, Muzafar A.;
Yadav, Santosh K.;
Krishnankutty, Roopesh;
Muralitharan, Shanmugakonar;
Al-Naemi, Hamda;
Bagga, Puneet;
Reddy, Ravinder;
Dhawan, Punita;
Akobeng, Anthony;
Uddin, Shahab;
Frenneaux, Michael P.;
El-Rifai, Wael;
Haris, Mohammad

Publication type:

Literature Review

An epidemiological risk assessment of imported malaria cases and potential local transmission in Qatar.

Published in:

European Journal of Public Health, 2025, v. 35, p. i35, doi. 10.1093/eurpub/ckae127

By:

Bansal, Devendra;
Assaad, Nada;
Mohamed, Hend Omar;
Shanmugakonar, Muralitharan;
Pacate, Dorothy;
Mohamed, Khider;
Balakrishnan, Perumal;
Ramiscal, Redentor Cuizon;
Ganesan, Nandakumar;
Al-Shamali, Maha Hammam M A;
Sultan, Ali A;
Munir, Waqar;
Abukhattab, Mohammed;
Schaffner, Francis;
Al-Maslamani, Muna A;
Al-Romaihi, Hamad Eid;
Al-Thani, Mohammed;
Khayat, Fatima Al;
Farag, Elmoubashar Abd

Publication type:

Article

Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis.

Published in:

Human Mutation, 1999, v. 14, n. 1, p. 80, doi. 10.1002/(SICI)1098-1004(1999)14:1<80::AID-HUMU10>3.0.CO;2-J

By:

Gabolde, Martine;
Muralitharan, Shanmugakonar;
Besmond, Claude

Publication type:

Article

Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic omani patients.

Published in:

American Journal of Hematology, 2007, v. 82, n. 12, p. 1099, doi. 10.1002/ajh.21009

By:

Muralitharan, Shanmugakonar;
Wali, Yasser A.;
Dennison, David;
Lamki, Zakia A.;
Zachariah, Mathew;
Nagwa, El Banna;
Pathare, Anil;
Krishnamoorthy, Rajagopal

Publication type:

Article

An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.

Published in:

American Journal of Hematology, 2005, v. 78, n. 1, p. 59

By:

Shanmugakonar Muralitharan;
Zakia Al Lamki;
David Dennison;
Brian Sidney Christie;
Yasser A. Wali;
Mathew Zachariah;
Marc Romana;
Riad Bayoumi;
Rajagopal Krishnamoorthy

Publication type:

Article

Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an association.

Published in:

American Journal of Hematology, 2004, v. 76, n. 3, p. 310, doi. 10.1002/ajh.20078

By:

Marc Romana;
Jean‐Pierre Diara;
Lydia Doumbo;
Shanmugakonar Muralitharan;
Rajendranath Ramasawmy;
Lysiane Keclard;
Vanessa Tarer;
Vicky Chaar;
Jacques Elion;
Rajagopal Krishnamoorthy;
John Clayton

Publication type:

Article