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Items: 13

1.

Ocimum sanctum leaf extracts attenuate human monocytic (THP-1) cell activation.

Choudhury SS, Bashyam L, Manthapuram N, Bitla P, Kollipara P, Tetali SD.

J Ethnopharmacol. 2014 May 28;154(1):148-55. doi: 10.1016/j.jep.2014.03.049. Epub 2014 Apr 13.

PMID:
24732112
2.

Physiological role of AOX1a in photosynthesis and maintenance of cellular redox homeostasis under high light in Arabidopsis thaliana.

Vishwakarma A, Bashyam L, Senthilkumaran B, Scheibe R, Padmasree K.

Plant Physiol Biochem. 2014 Aug;81:44-53. doi: 10.1016/j.plaphy.2014.01.019. Epub 2014 Feb 6.

PMID:
24560882
3.

Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutation.

Bashyam MD, Chaudhary AK, Kiran M, Reddy V, Nagarajaram HA, Dalal A, Bashyam L, Suri D, Gupta A, Gupta N, Kabra M, Puri RD, RamaDevi R, Kapoor S, Danda S.

Clin Genet. 2014 Dec;86(6):530-8. doi: 10.1111/cge.12316. Epub 2013 Dec 20.

PMID:
24355074
4.

Splice, insertion-deletion and nonsense mutations that perturb the phenylalanine hydroxylase transcript cause phenylketonuria in India.

Bashyam MD, Chaudhary AK, Kiran M, Nagarajaram HA, Devi RR, Ranganath P, Dalal A, Bashyam L, Gupta N, Kabra M, Muranjan M, Puri RD, Verma IC, Nampoothiri S, Kadandale JS.

J Cell Biochem. 2014 Mar;115(3):566-74. doi: 10.1002/jcb.24692.

PMID:
24130151
5.

Stem-bark of Terminalia arjuna attenuates human monocytic (THP-1) and aortic endothelial cell activation.

Kokkiripati PK, Kamsala RV, Bashyam L, Manthapuram N, Bitla P, Peddada V, Raghavendra AS, Tetali SD.

J Ethnopharmacol. 2013 Mar 27;146(2):456-64. doi: 10.1016/j.jep.2012.12.050. Epub 2013 Jan 24.

PMID:
23353898
6.

Evidence for possible non-canonical pathway(s) driven early-onset colorectal cancer in India.

Raman R, Kotapalli V, Adduri R, Gowrishankar S, Bashyam L, Chaudhary A, Vamsy M, Patnaik S, Srinivasulu M, Sastry R, Rao S, Vasala A, Kalidindi N, Pollack J, Murthy S, Bashyam M.

Mol Carcinog. 2014 Feb;53 Suppl 1:E181-6. doi: 10.1002/mc.21976. Epub 2012 Nov 20.

7.

Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1β.

Bashyam MD, Chaudhary AK, Sinha M, Nagarajaram HA, Devi AR, Bashyam L, Reddy EC, Dalal A.

J Cell Biochem. 2012 Oct;113(10):3122-32. doi: 10.1002/jcb.24189.

PMID:
22593002
8.

Endosulfan and flutamide, alone and in combination, target ovarian growth in juvenile catfish, Clarias batrachus.

Chakrabarty S, Rajakumar A, Raghuveer K, Sridevi P, Mohanachary A, Prathibha Y, Bashyam L, Dutta-Gupta A, Senthilkumaran B.

Comp Biochem Physiol C Toxicol Pharmacol. 2012 Apr;155(3):491-7. doi: 10.1016/j.cbpc.2011.12.007. Epub 2011 Dec 28.

PMID:
22227439
9.

A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India.

Bashyam MD, Chaudhary AK, Reddy EC, Reddy V, Acharya V, Nagarajaram HA, Devi AR, Bashyam L, Dalal AB, Gupta N, Kabra M, Agarwal M, Phadke SR, Tainwala R, Kumar R, Hariharan SV.

Br J Dermatol. 2012 Apr;166(4):819-29. doi: 10.1111/j.1365-2133.2011.10707.x. Epub 2012 Mar 5.

PMID:
22032522
10.

Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA.

Bashyam MD, Chaudhary AK, Reddy EC, Devi AR, Savithri GR, Ratheesh R, Bashyam L, Mahesh E, Sen D, Puri R, Verma IC, Nampoothiri S, Vaidyanathan S, Chandrashekar MD, Kantheti P.

Mol Genet Metab. 2010 May;100(1):96-9. doi: 10.1016/j.ymgme.2010.01.016. Epub 2010 Feb 2. Erratum in: Mol Genet Metab. 2010 Aug;100(4):390. Verma, Inder C [corrected to Verma, Ishwar C].

PMID:
20188615
11.

Frequent occult infection with Cytomegalovirus in cardiac transplant recipients despite antiviral prophylaxis.

Potena L, Holweg CT, Vana ML, Bashyam L, Rajamani J, McCormick AL, Cooke JP, Valantine HA, Mocarski ES.

J Clin Microbiol. 2007 Jun;45(6):1804-10. Epub 2007 Apr 4. Erratum in: J Clin Microbiol. 2008 Dec;46(12):4121.

12.

Molecular genetic analyses of beta-thalassemia in South India reveals rare mutations in the beta-globin gene.

Bashyam MD, Bashyam L, Savithri GR, Gopikrishna M, Sangal V, Devi AR.

J Hum Genet. 2004;49(8):408-13. Epub 2004 Jul 24.

PMID:
15278762
13.

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation.

Saleem Q, Choudhry S, Mukerji M, Bashyam L, Padma MV, Chakravarthy A, Maheshwari MC, Jain S, Brahmachari SK.

Hum Genet. 2000 Feb;106(2):179-87.

PMID:
10746559

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