Satyamoorthy K - Search Results

1

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type.

Girisha KM, Shrikiran A, Bidchol AM, Sakamoto O, Gopinath PM, Satyamoorthy K. Girisha KM, et al. Among authors: satyamoorthy k. Indian J Hum Genet. 2012 Sep;18(3):346-8. doi: 10.4103/0971-6866.108025. Indian J Hum Genet. 2012. PMID: 23716945 Free PMC article.

2

Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of β-thalassemia.

Saadi AV, Girisha KM, Gopinath PM, Satyamoorthy K. Saadi AV, et al. Among authors: satyamoorthy k. Transl Res. 2011 Mar;157(3):150-5. doi: 10.1016/j.trsl.2010.12.005. Epub 2011 Jan 12. Transl Res. 2011. PMID: 21316031

3

Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.

Girisha KM, Vasudevan TG, Saadi AV, Shah H, Gopinath PM, Satyamoorthy K. Girisha KM, et al. Among authors: satyamoorthy k. Clin Dysmorphol. 2011 Oct;20(4):205-209. doi: 10.1097/MCD.0b013e328348d956. Clin Dysmorphol. 2011. PMID: 21716096 No abstract available.

4

Comprehensive DNA copy number profile and BAC library construction of an Indian individual.

Chakrabarty S, D'Souza RR, Bellampalli R, Rotti H, Saadi AV, Gopinath PM, Acharya RV, Govindaraj P, Thangaraj K, Satyamoorthy K. Chakrabarty S, et al. Among authors: satyamoorthy k. Gene. 2012 Jun 1;500(2):186-93. doi: 10.1016/j.gene.2012.03.054. Epub 2012 Mar 21. Gene. 2012. PMID: 22465536

5

Mucolipidosis type II α/β with a homozygous missense mutation in the GNPTAB gene.

Coutinho MF, Santos Lda S, Girisha KM, Satyamoorthy K, Lacerda L, Prata MJ, Alves S. Coutinho MF, et al. Among authors: satyamoorthy k. Am J Med Genet A. 2012 May;158A(5):1225-8. doi: 10.1002/ajmg.a.35295. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495880 No abstract available.

6

Brahmarasayana protects against Ethyl methanesulfonate or Methyl methanesulfonate induced chromosomal aberrations in mouse bone marrow cells.

Guruprasad KP, Subramanian A, Singh VJ, Sharma RS, Gopinath PM, Sewram V, Varier PM, Satyamoorthy K. Guruprasad KP, et al. Among authors: satyamoorthy k. BMC Complement Altern Med. 2012 Aug 1;12:113. doi: 10.1186/1472-6882-12-113. BMC Complement Altern Med. 2012. PMID: 22853637 Free PMC article.

7

Thiopurine S-methyltransferase alleles, TPMT(*)2, (*)3B and (*)3C, and genotype frequencies in an Indian population.

Murugesan R, Vahab SA, Patra S, Rao R, Rao J, Rai P, Gopinath PM, Satyamoorthy K. Murugesan R, et al. Among authors: satyamoorthy k. Exp Ther Med. 2010 Jan;1(1):121-127. doi: 10.3892/etm_00000021. Epub 2010 Jan 1. Exp Ther Med. 2010. PMID: 23136604 Free PMC article.

8

Mitochondrial DNA variation analysis in cervical cancer.

Kabekkodu SP, Bhat S, Mascarenhas R, Mallya S, Bhat M, Pandey D, Kushtagi P, Thangaraj K, Gopinath PM, Satyamoorthy K. Kabekkodu SP, et al. Among authors: satyamoorthy k. Mitochondrion. 2014 May;16:73-82. doi: 10.1016/j.mito.2013.07.001. Epub 2013 Jul 10. Mitochondrion. 2014. PMID: 23851045

9

Single nucleotide polymorphisms of ADRB2 gene and their association with susceptibility for Plasmodium falciparum malaria and asthma in an Indian population.

Saadi AV, Gupta H, Angural A, Dhanya SK, Mony S, Oberoi D, D'Souza SC, Sahoo RC, Hande MH, Gopinath PM, Satyamoorthy K. Saadi AV, et al. Among authors: satyamoorthy k. Infect Genet Evol. 2013 Dec;20:140-7. doi: 10.1016/j.meegid.2013.08.026. Epub 2013 Sep 4. Infect Genet Evol. 2013. PMID: 24012958

10

A novel frameshift mutation in TWIST2 gene causing Setleis syndrome.

Girisha KM, Bidchol AM, Sarpangala MK, Satyamoorthy K. Girisha KM, et al. Among authors: satyamoorthy k. Indian J Pediatr. 2014 Mar;81(3):302-4. doi: 10.1007/s12098-013-1253-y. Epub 2013 Oct 15. Indian J Pediatr. 2014. PMID: 24127007

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