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Items: 15

1.

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

Bhat AA, Syed N, Therachiyil L, Nisar S, Hashem S, Macha MA, Yadav SK, Krishnankutty R, Muralitharan S, Al-Naemi H, Bagga P, Reddy R, Dhawan P, Akobeng A, Uddin S, Frenneaux MP, El-Rifai W, Haris M.

Int J Mol Sci. 2020 Jan 15;21(2). pii: E569. doi: 10.3390/ijms21020569. Review.

2.

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

Bhat AA, Uppada S, Achkar IW, Hashem S, Yadav SK, Shanmugakonar M, Al-Naemi HA, Haris M, Uddin S.

Front Physiol. 2019 Jan 23;9:1942. doi: 10.3389/fphys.2018.01942. eCollection 2018. Review.

3.

RAS-mediated oncogenic signaling pathways in human malignancies.

Khan AQ, Kuttikrishnan S, Siveen KS, Prabhu KS, Shanmugakonar M, Al-Naemi HA, Haris M, Dermime S, Uddin S.

Semin Cancer Biol. 2019 Feb;54:1-13. doi: 10.1016/j.semcancer.2018.03.001. Epub 2018 Mar 7. Review.

PMID:
29524560
4.

CARMA2sh and ULK2 control pathogen-associated molecular patterns recognition in human keratinocytes: psoriasis-linked CARMA2sh mutants escape ULK2 censorship.

Scudiero I, Mazzone P, D'Andrea LE, Ferravante A, Zotti T, Telesio G, De Rubis G, Reale C, Pizzulo M, Muralitharan S, Vito P, Stilo R.

Cell Death Dis. 2017 Feb 23;8(2):e2627. doi: 10.1038/cddis.2017.51.

5.

NF-κB Essential Modulator (NEMO) Is Critical for Thyroid Function.

Reale C, Iervolino A, Scudiero I, Ferravante A, D'Andrea LE, Mazzone P, Zotti T, Leonardi A, Roberto L, Zannini M, de Cristofaro T, Shanmugakonar M, Capasso G, Pasparakis M, Vito P, Stilo R.

J Biol Chem. 2016 Mar 11;291(11):5765-73. doi: 10.1074/jbc.M115.711697. Epub 2016 Jan 19.

6.

Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolate.

Turnbull J, Kumar S, Ren ZP, Muralitharan S, Naranian T, Ackerley CA, Minassian BA.

J Child Neurol. 2008 Feb;23(2):240-2. doi: 10.1177/0883073807309245.

PMID:
18263761
7.

Clinical and genetic study of spinal muscular atrophies in Oman.

Koul R, Al Futaisi A, Chacko A, Rao V, Simsek M, Muralitharan S, Ganguly SS, Bayoumi R.

J Child Neurol. 2007 Oct;22(10):1227-30.

PMID:
17940251
8.

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

Muralitharan S, Wali YA, Dennison D, Lamki ZA, Zachariah M, Nagwa el B, Pathare A, Krishnamoorthy R.

Am J Hematol. 2007 Dec;82(12):1099-102.

9.

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.

Hempelmann A, Kumar S, Muralitharan S, Sander T.

Neurosci Lett. 2006 Jul 10;402(1-2):118-20. Epub 2006 Apr 24.

PMID:
16632198
10.

Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemia.

Al-Lamki Z, Wali YA, Wasifuddin SM, Zachariah M, Al-Mjeni R, Li C, Muralitharan S, Al-Kharusi K, Gunaratne P, Peterson L, Gibbs R, Gingras MC, Margolin JF.

Pediatr Hematol Oncol. 2005 Oct-Nov;22(7):629-43.

PMID:
16166056
11.

Trinucleotide repeat analysis of spinocerebellar ataxia patients in Oman.

Chacko JP, Muralitharan S, Al-Ansari A, Al-Kharusi K, Al-Asmi A, Pratap CR, Bayoumi R.

Neurosciences (Riyadh). 2005 Jan;10(1):61-3.

PMID:
22473187
12.

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

Muralitharan S, Al Lamki Z, Dennison D, Christie BS, Wali YA, Zachariah M, Romana M, Bayoumi R, Krishnamoorthy R.

Am J Hematol. 2005 Jan;78(1):59-63.

13.

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

Romana M, Diara JP, Doumbo L, Muralitharan S, Ramasawmy R, Keclard L, Tarer V, Chaar V, Elion J, Krishnamoorthy R, Clayton J.

Am J Hematol. 2004 Jul;76(3):310-1. No abstract available.

14.

Allele-specific amplification of exon 7 in the survival motor neuron (SMN) genes for molecular diagnosis of spinal muscular atrophy.

Simsek M, Al-Bulushi T, Shanmugakonar M, Al-Barwani HS, Bayoumi R.

Genet Test. 2003 Winter;7(4):325-7.

PMID:
15000810
15.

Beta-globin-like gene cluster haplotypes in hemoglobinopathies.

Muralitharan S, Krishnamoorthy R, Nagel RL.

Methods Mol Med. 2003;82:195-211. No abstract available.

PMID:
12669645

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