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Items: 1 to 50 of 275

1.

An Ancient Harappan Genome Lacks Ancestry from Steppe Pastoralists or Iranian Farmers.

Shinde V, Narasimhan VM, Rohland N, Mallick S, Mah M, Lipson M, Nakatsuka N, Adamski N, Broomandkhoshbacht N, Ferry M, Lawson AM, Michel M, Oppenheimer J, Stewardson K, Jadhav N, Kim YJ, Chatterjee M, Munshi A, Panyam A, Waghmare P, Yadav Y, Patel H, Kaushik A, Thangaraj K, Meyer M, Patterson N, Rai N, Reich D.

Cell. 2019 Oct 17;179(3):729-735.e10. doi: 10.1016/j.cell.2019.08.048. Epub 2019 Sep 5.

PMID:
31495572
2.

The formation of human populations in South and Central Asia.

Narasimhan VM, Patterson N, Moorjani P, Rohland N, Bernardos R, Mallick S, Lazaridis I, Nakatsuka N, Olalde I, Lipson M, Kim AM, Olivieri LM, Coppa A, Vidale M, Mallory J, Moiseyev V, Kitov E, Monge J, Adamski N, Alex N, Broomandkhoshbacht N, Candilio F, Callan K, Cheronet O, Culleton BJ, Ferry M, Fernandes D, Freilich S, Gamarra B, Gaudio D, Hajdinjak M, Harney É, Harper TK, Keating D, Lawson AM, Mah M, Mandl K, Michel M, Novak M, Oppenheimer J, Rai N, Sirak K, Slon V, Stewardson K, Zalzala F, Zhang Z, Akhatov G, Bagashev AN, Bagnera A, Baitanayev B, Bendezu-Sarmiento J, Bissembaev AA, Bonora GL, Chargynov TT, Chikisheva T, Dashkovskiy PK, Derevianko A, Dobeš M, Douka K, Dubova N, Duisengali MN, Enshin D, Epimakhov A, Fribus AV, Fuller D, Goryachev A, Gromov A, Grushin SP, Hanks B, Judd M, Kazizov E, Khokhlov A, Krygin AP, Kupriyanova E, Kuznetsov P, Luiselli D, Maksudov F, Mamedov AM, Mamirov TB, Meiklejohn C, Merrett DC, Micheli R, Mochalov O, Mustafokulov S, Nayak A, Pettener D, Potts R, Razhev D, Rykun M, Sarno S, Savenkova TM, Sikhymbaeva K, Slepchenko SM, Soltobaev OA, Stepanova N, Svyatko S, Tabaldiev K, Teschler-Nicola M, Tishkin AA, Tkachev VV, Vasilyev S, Velemínský P, Voyakin D, Yermolayeva A, Zahir M, Zubkov VS, Zubova A, Shinde VS, Lalueza-Fox C, Meyer M, Anthony D, Boivin N, Thangaraj K, Kennett DJ, Frachetti M, Pinhasi R, Reich D.

Science. 2019 Sep 6;365(6457). pii: eaat7487. doi: 10.1126/science.aat7487.

3.

Orientin Induces G0/G1 Cell Cycle Arrest and Mitochondria Mediated Intrinsic Apoptosis in Human Colorectal Carcinoma HT29 Cells.

Thangaraj K, Balasubramanian B, Park S, Natesan K, Liu W, Manju V.

Biomolecules. 2019 Aug 27;9(9). pii: E418. doi: 10.3390/biom9090418.

4.

Ancient DNA from the skeletons of Roopkund Lake reveals Mediterranean migrants in India.

Harney É, Nayak A, Patterson N, Joglekar P, Mushrif-Tripathy V, Mallick S, Rohland N, Sedig J, Adamski N, Bernardos R, Broomandkhoshbacht N, Culleton BJ, Ferry M, Harper TK, Michel M, Oppenheimer J, Stewardson K, Zhang Z, Harashawaradhana, Bartwal MS, Kumar S, Diyundi SC, Roberts P, Boivin N, Kennett DJ, Thangaraj K, Reich D, Rai N.

Nat Commun. 2019 Aug 20;10(1):3670. doi: 10.1038/s41467-019-11357-9.

5.

Homozygous R627W mutations in POLG cause mitochondrial DNA depletion leading to encephalopathy, seizures and stroke-like episodes.

Paramasivam A, Venkatapathi C, Sandeep G, Meena AK, Uppin MS, Mohapatra S, Pitceathly RDS, Thangaraj K.

Mitochondrion. 2019 Sep;48:78-83. doi: 10.1016/j.mito.2019.08.003. Epub 2019 Aug 16.

PMID:
31425757
6.

Peopling of India: Ancient DNA perspectives.

Thangaraj K, Rai N.

J Biosci. 2019 Jul;44(3). pii: 70.

7.

Corrigendum to "Mitochondria in health and disease" [Mitochondrion 43(2018) 25-29].

Chakrabarty S, Kabekkodu SP, Singh RP, Thangaraj K, Singh KK, Satyamoorthy K.

Mitochondrion. 2019 Jul;47:331. doi: 10.1016/j.mito.2019.06.006. Epub 2019 Jun 22. No abstract available.

PMID:
31235268
8.

The peopling of Lakshadweep Archipelago.

Mustak MS, Rai N, Naveen MR, Prakash S, Carlus SJ, Pasupuleti N, Srivastava A, Singh PP, Babu I, Dubey PK, Chaubey G, Thangaraj K.

Sci Rep. 2019 May 6;9(1):6968. doi: 10.1038/s41598-019-43384-3.

9.

High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men.

Rani DS, Rajender S, Pavani K, Chaubey G, Rasalkar AA, Gupta NJ, Deendayal M, Chakravarty B, Thangaraj K.

Sci Rep. 2019 Apr 18;9(1):6276. doi: 10.1038/s41598-019-42690-0.

10.

Mitochondrial genome variations in idiopathic dilated cardiomyopathy.

Govindaraj P, Rani B, Sundaravadivel P, Vanniarajan A, Indumathi KP, Khan NA, Dhandapany PS, Rani DS, Tamang R, Bahl A, Narasimhan C, Rakshak D, Rathinavel A, Premkumar K, Khullar M, Thangaraj K.

Mitochondrion. 2019 Sep;48:51-59. doi: 10.1016/j.mito.2019.03.003. Epub 2019 Mar 22.

PMID:
30910572
11.

Retinoblastoma discordance in families with twins.

Abraham A, Thirumalairaj K, Gaikwad N, Muthukkaruppan V, Reddy AG, Thangaraj K, Kim U, Vanniarajan A.

Indian J Ophthalmol. 2019 Mar;67(3):436-439. doi: 10.4103/ijo.IJO_1245_18.

12.

Variations in macrophage migration inhibitory factor gene are not associated with visceral leishmaniasis in India.

Mishra A, Sundaravadivel P, Tripathi SK, Jha RK, Badrukhiya J, Basak N, Anerao I, Sharma A, Idowu AE, Mishra A, Pandey S, Kumar U, Singh S, Nizamuddin S, Tupperwar NC, Jha AN, Thangaraj K.

J Infect Public Health. 2019 May - Jun;12(3):380-387. doi: 10.1016/j.jiph.2018.12.011. Epub 2019 Jan 2.

13.

A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.

Rani DS, Nallari P, Rani J, Nizamuddin S, Seelamneni T, Narasimhan C, Thangaraj K.

Cardiology. 2018;141(3):156-166. doi: 10.1159/000495027. Epub 2019 Jan 3.

PMID:
30605904
14.

Orientin mitigates 1, 2-dimethylhydrazine induced lipid peroxidation, antioxidant and biotransforming bacterial enzyme alterations in experimental rats.

Thangaraj K, Natesan K, Settu K, Palani M, Govindarasu M, Subborayan V, Vaiyapuri M.

J Cancer Res Ther. 2018 Oct-Dec;14(6):1379-1388. doi: 10.4103/jcrt.JCRT_1363_16.

15.

SNPs in ERCC1, ERCC2, and XRCC1 genes of the DNA repair pathway and risk of male infertility in the Asian populations: association study, meta-analysis, and trial sequential analysis.

Singh V, Bansal SK, Sudhakar DVS, Neelabh, Chakraborty A, Trivedi S, Gupta G, Thangaraj K, Rajender S, Singh K.

J Assist Reprod Genet. 2019 Jan;36(1):79-90. doi: 10.1007/s10815-018-1339-6. Epub 2018 Nov 3.

16.

Orientin, a flavanoid, mitigates 1, 2 dimethylhydrazine-induced colorectal lesions in Wistar rats fed a high-fat diet.

Thangaraj K, Natesan K, Palani M, Vaiyapuri M.

Toxicol Rep. 2018 Sep 27;5:977-987. doi: 10.1016/j.toxrep.2018.09.004. eCollection 2018.

17.

Report of Phoma herbarum Causing Leaf Spot Disease of Camellia sinensis in China.

Thangaraj K, Deng C, Cheng LL, Deng WW, Zhang ZZ.

Plant Dis. 2018 Aug 28:PDIS01180121PDN. doi: 10.1094/PDIS-01-18-0121-PDN. [Epub ahead of print] No abstract available.

18.

The influences of genes, the environment, and social factors on the evolution of skin color diversity in India.

Iliescu FM, Chaplin G, Rai N, Jacobs GS, Basu Mallick C, Mishra A, Thangaraj K, Jablonski NG.

Am J Hum Biol. 2018 Sep;30(5):e23170. doi: 10.1002/ajhb.23170. Epub 2018 Aug 12.

PMID:
30099804
19.

Raised plasma levels of H2S and nitrate predict intrapulmonary vascular dilations: A preliminary report in patients with cryptogenic cirrhosis.

Bera C, Thangaraj K, Pati PK, Ramachandran J, Balasubramanian KA, Ramachandran A, Zachariah U, Sajith KG, Goel A, Eapen CE.

Indian J Gastroenterol. 2018 May;37(3):209-214. doi: 10.1007/s12664-018-0862-9. Epub 2018 Jul 9.

PMID:
29984390
20.

Mitochondria in health and disease.

Chakrabarty S, Kabekkodu SP, Singh RP, Thangaraj K, Singh KK, Satyamoorthy K.

Mitochondrion. 2018 Nov;43:25-29. doi: 10.1016/j.mito.2018.06.006. Epub 2018 Jun 23. Erratum in: Mitochondrion. 2019 Jul;47:331.

PMID:
29944924
21.

Reconstructing the demographic history of the Himalayan and adjoining populations.

Tamang R, Chaubey G, Nandan A, Govindaraj P, Singh VK, Rai N, Mallick CB, Sharma V, Sharma VK, Shah AM, Lalremruata A, Reddy AG, Rani DS, Doviah P, Negi N, Hadid Y, Pande V, Vishnupriya S, van Driem G, Behar DM, Sharma T, Singh L, Villems R, Thangaraj K.

Hum Genet. 2018 Feb;137(2):129-139. doi: 10.1007/s00439-018-1867-2. Epub 2018 Jan 22.

PMID:
29356938
22.

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate.

Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.

Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):382. doi: 10.1167/iovs.17-23468. No abstract available.

PMID:
29346803
23.

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.

Bindu PS, Sonam K, Govindaraj P, Govindaraju C, Chiplunkar S, Nagappa M, Kumar R, Vekhande CC, Arvinda HR, Gayathri N, Srinivas Bharath MM, Ponmalar JNJ, Philip M, Vandana VP, Khan NA, Nunia V, Paramasivam A, Sinha S, Thangaraj K, Taly AB.

Clin Neurol Neurosurg. 2018 Jan;164:182-189. doi: 10.1016/j.clineuro.2017.12.010. Epub 2017 Dec 9.

PMID:
29272804
24.

NR5A1 mutations are not associated with male infertility in Indian men.

Sudhakar DVS, Nizamuddin S, Manisha G, Devi JR, Gupta NJ, Chakravarthy BN, Deenadayal M, Singh L, Thangaraj K.

Andrologia. 2018 Apr;50(3). doi: 10.1111/and.12931. Epub 2017 Dec 18.

PMID:
29265478
25.
26.

Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.

Chaubey G, Tamang R, Pennarun E, Dubey P, Rai N, Upadhyay RK, Meena RP, Patel JR, van Driem G, Thangaraj K, Metspalu M, Villems R.

Eur J Hum Genet. 2017 Nov;25(11):1291. doi: 10.1038/ejhg.2017.46.

27.

Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility.

Gupta N, Sudhakar DVS, Gangwar PK, Sankhwar SN, Gupta NJ, Chakraborty B, Thangaraj K, Gupta G, Rajender S.

Sci Rep. 2017 Sep 11;7(1):11225. doi: 10.1038/s41598-017-10866-1.

28.

Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.

Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.

Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):3923-3930. doi: 10.1167/iovs.16-20695.

PMID:
28768321
29.

The promise of discovering population-specific disease-associated genes in South Asia.

Nakatsuka N, Moorjani P, Rai N, Sarkar B, Tandon A, Patterson N, Bhavani GS, Girisha KM, Mustak MS, Srinivasan S, Kaushik A, Vahab SA, Jagadeesh SM, Satyamoorthy K, Singh L, Reich D, Thangaraj K.

Nat Genet. 2017 Sep;49(9):1403-1407. doi: 10.1038/ng.3917. Epub 2017 Jul 17.

30.

MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report.

Pyal A, Paramasivam A, Meena AK, Bhavana VB, Thangaraj K.

Mitochondrion. 2017 Nov;37:41-45. doi: 10.1016/j.mito.2017.06.006. Epub 2017 Jun 30.

PMID:
28673863
31.

"Like sugar in milk": reconstructing the genetic history of the Parsi population.

Chaubey G, Ayub Q, Rai N, Prakash S, Mushrif-Tripathy V, Mezzavilla M, Pathak AK, Tamang R, Firasat S, Reidla M, Karmin M, Rani DS, Reddy AG, Parik J, Metspalu E, Rootsi S, Dalal K, Khaliq S, Mehdi SQ, Singh L, Metspalu M, Kivisild T, Tyler-Smith C, Villems R, Thangaraj K.

Genome Biol. 2017 Jun 14;18(1):110. doi: 10.1186/s13059-017-1244-9.

32.

Geographical distribution of complement receptor type 1 variants and their associated disease risk.

Lucas Sandri T, Adukpo S, Giang DP, Nguetse CN, Antunes Andrade F, Tong HV, Toan NL, Song LH, Elumalai P, Thangaraj K, Valluri VL, Ntoumi F, Meyer CG, Jose de Messias Reason I, Kremsner PG, Velavan TP.

PLoS One. 2017 May 17;12(5):e0175973. doi: 10.1371/journal.pone.0175973. eCollection 2017.

33.

Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Bugiardini E, Poole OV, Manole A, Pittman AM, Horga A, Hargreaves I, Woodward CE, Sweeney MG, Holton JL, Taanman JW, Plant GT, Poulton J, Zeviani M, Ghezzi D, Taylor J, Smith C, Fratter C, Kanikannan MA, Paramasivam A, Thangaraj K, Spinazzola A, Holt IJ, Houlden H, Hanna MG, Pitceathly RDS.

Neurol Genet. 2017 May 2;3(3):e149. doi: 10.1212/NXG.0000000000000149. eCollection 2017 Jun.

34.

3'-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.

Karthi S, Rajeshwari M, Francis A, Saravanan M, Varalakshmi P, Houlden H, Thangaraj K, Ashokkumar B.

Clin Chim Acta. 2017 Aug;471:46-54. doi: 10.1016/j.cca.2017.05.016. Epub 2017 May 11.

PMID:
28502559
35.

Origin and spread of human mitochondrial DNA haplogroup U7.

Sahakyan H, Hooshiar Kashani B, Tamang R, Kushniarevich A, Francis A, Costa MD, Pathak AK, Khachatryan Z, Sharma I, van Oven M, Parik J, Hovhannisyan H, Metspalu E, Pennarun E, Karmin M, Tamm E, Tambets K, Bahmanimehr A, Reisberg T, Reidla M, Achilli A, Olivieri A, Gandini F, Perego UA, Al-Zahery N, Houshmand M, Sanati MH, Soares P, Rai E, Šarac J, Šarić T, Sharma V, Pereira L, Fernandes V, Černý V, Farjadian S, Singh DP, Azakli H, Üstek D, Ekomasova Trofimova N, Kutuev I, Litvinov S, Bermisheva M, Khusnutdinova EK, Rai N, Singh M, Singh VK, Reddy AG, Tolk HV, Cvjetan S, Lauc LB, Rudan P, Michalodimitrakis EN, Anagnou NP, Pappa KI, Golubenko MV, Orekhov V, Borinskaya SA, Kaldma K, Schauer MA, Simionescu M, Gusar V, Grechanina E, Govindaraj P, Voevoda M, Damba L, Sharma S, Singh L, Semino O, Behar DM, Yepiskoposyan L, Richards MB, Metspalu M, Kivisild T, Thangaraj K, Endicott P, Chaubey G, Torroni A, Villems R.

Sci Rep. 2017 Apr 7;7:46044. doi: 10.1038/srep46044.

36.

Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.

Jain S, Rai N, Kumar G, Pruthi PA, Thangaraj K, Bajpai S, Pruthi V.

PLoS One. 2017 Mar 8;12(3):e0164823. doi: 10.1371/journal.pone.0164823. eCollection 2017.

37.

Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.

Chaubey G, Tamang R, Pennarun E, Dubey P, Rai N, Upadhyay RK, Meena RP, Patel JR, van Driem G, Thangaraj K, Metspalu M, Villems R.

Eur J Hum Genet. 2017 Apr;25(4):493-498. doi: 10.1038/ejhg.2016.198. Epub 2017 Feb 1. Erratum in: Eur J Hum Genet. 2017 Nov;25(11):1291.

38.

Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.

Mishra A, Nizammuddin S, Mallick CB, Singh S, Prakash S, Siddiqui NA, Rai N, Carlus SJ, Sudhakar DVS, Tripathi VP, Möls M, Kim-Howard X, Dewangan H, Mishra A, Reddy AG, Roy B, Pandey K, Chaubey G, Das P, Nath SK, Singh L, Thangaraj K.

J Invest Dermatol. 2017 Mar;137(3):670-677. doi: 10.1016/j.jid.2016.10.043. Epub 2016 Nov 17.

39.

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Sonam K, Bindu PS, Srinivas Bharath MM, Govindaraj P, Gayathri N, Arvinda HR, Chiplunkar S, Nagappa M, Sinha S, Khan NA, Nunia V, Paramasivam A, Thangaraj K, Taly AB.

Mitochondrion. 2017 Jan;32:42-49. doi: 10.1016/j.mito.2016.11.002. Epub 2016 Nov 5.

PMID:
27826120
40.

Plasma hydrogen sulphide does not predict severity of acute pancreatitis in humans.

Qureshi IN, David D, Thangaraj KR, Kurien RT, Chowdhury SD, Goel A, Dutta AK, Simon EG, Ramachandran A, Balasubramanian KA, Joseph AJ.

Indian J Gastroenterol. 2016 Nov;35(6):478-481. Epub 2016 Oct 29.

PMID:
27796938
41.

c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Ganesan M, Nizamuddin S, Katkam SK, Kumaraswami K, Hosad UK, Lobo LL, Kutala VK, Thangaraj K.

PLoS One. 2016 Oct 21;11(10):e0164151. doi: 10.1371/journal.pone.0164151. eCollection 2016.

42.

Corrigendum: The paternal ancestry of Uttarakhand does not imitate the classical caste system of India.

Negi N, Tamang R, Pande V, Sharma A, Shah A, Reddy AG, Vishnupriya S, Singh L, Chaubey G, Thangaraj K.

J Hum Genet. 2016 Sep;61(9):843. doi: 10.1038/jhg.2016.48. No abstract available.

PMID:
27666120
43.

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.

Mallick S, Li H, Lipson M, Mathieson I, Gymrek M, Racimo F, Zhao M, Chennagiri N, Nordenfelt S, Tandon A, Skoglund P, Lazaridis I, Sankararaman S, Fu Q, Rohland N, Renaud G, Erlich Y, Willems T, Gallo C, Spence JP, Song YS, Poletti G, Balloux F, van Driem G, de Knijff P, Romero IG, Jha AR, Behar DM, Bravi CM, Capelli C, Hervig T, Moreno-Estrada A, Posukh OL, Balanovska E, Balanovsky O, Karachanak-Yankova S, Sahakyan H, Toncheva D, Yepiskoposyan L, Tyler-Smith C, Xue Y, Abdullah MS, Ruiz-Linares A, Beall CM, Di Rienzo A, Jeong C, Starikovskaya EB, Metspalu E, Parik J, Villems R, Henn BM, Hodoglugil U, Mahley R, Sajantila A, Stamatoyannopoulos G, Wee JT, Khusainova R, Khusnutdinova E, Litvinov S, Ayodo G, Comas D, Hammer MF, Kivisild T, Klitz W, Winkler CA, Labuda D, Bamshad M, Jorde LB, Tishkoff SA, Watkins WS, Metspalu M, Dryomov S, Sukernik R, Singh L, Thangaraj K, Pääbo S, Kelso J, Patterson N, Reich D.

Nature. 2016 Oct 13;538(7624):201-206. doi: 10.1038/nature18964. Epub 2016 Sep 21.

44.

Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up.

Vandana VP, Bindu PS, Sonam K, Govindaraj P, Chiplunkar S, Gayathri N, Govindaraj C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K, Taly AB.

Clin Neurol Neurosurg. 2016 Nov;150:198-199. doi: 10.1016/j.clineuro.2016.08.030. Epub 2016 Aug 31. No abstract available.

PMID:
27600858
45.

Genotype-phenotype correlation in long QT syndrome families.

Qureshi SF, Ali A, Venkateshwari A, Rao H, Jayakrishnan MP, Narasimhan C, Shenthar J, Thangaraj K, Nallari P.

Indian Pacing Electrophysiol J. 2015 Dec 17;15(6):269-85. doi: 10.1016/j.ipej.2015.12.001. eCollection 2015 Nov-Dec.

46.

Cryptic Eimeria genotypes are common across the southern but not northern hemisphere.

Clark EL, Macdonald SE, Thenmozhi V, Kundu K, Garg R, Kumar S, Ayoade S, Fornace KM, Jatau ID, Moftah A, Nolan MJ, Sudhakar NR, Adebambo AO, Lawal IA, Álvarez Zapata R, Awuni JA, Chapman HD, Karimuribo E, Mugasa CM, Namangala B, Rushton J, Suo X, Thangaraj K, Srinivasa Rao AS, Tewari AK, Banerjee PS, Dhinakar Raj G, Raman M, Tomley FM, Blake DP.

Int J Parasitol. 2016 Aug;46(9):537-44. doi: 10.1016/j.ijpara.2016.05.006. Epub 2016 Jun 29.

47.

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Vandana VP, Bindu PS, Sonam K, Govindaraj P, Taly AB, Gayathri N, Chiplunkar S, Govindaraju C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K.

Clin Neurol Neurosurg. 2016 Sep;148:17-21. doi: 10.1016/j.clineuro.2016.04.024. Epub 2016 Jun 14.

PMID:
27359089
48.

A rough set based rational clustering framework for determining correlated genes.

Jeyaswamidoss JE, Thangaraj K, Ramar K, Chitra M.

Acta Microbiol Immunol Hung. 2016 Jun;63(2):185-201. doi: 10.1556/030.63.2016.2.4.

PMID:
27352972
49.

Plasma Citrulline, Glycans, and Hydrogen Sulfide in Patients With Acute Pancreatitis: Possible Markers of Intestinal Damage.

Thangaraj KR, Priyadarshini SJ, Qureshi IN, Joseph AJ, Balasubramanian KA, Ramachandran A.

Pancreas. 2016 Jul;45(6):e27-9. doi: 10.1097/MPA.0000000000000593. No abstract available.

PMID:
27295536
50.

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.

Rai E, Mahajan A, Kumar P, Angural A, Dhar MK, Razdan S, Thangaraj K, Wise CA, Ikegawa S, Pandita KK, Sharma S.

Sci Rep. 2016 Jun 13;6:27684. doi: 10.1038/srep27684.

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