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Items: 1 to 50 of 262

1.

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.

2.

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. 2018 Nov 3. doi: 10.1007/s10815-018-1339-6. [Epub ahead of print]

PMID:
30390177
3.

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.

4.

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.

5.

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
6.

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
7.

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. Review.

PMID:
29944924
8.

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
9.

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
10.

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
11.

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
12.
13.

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.

14.

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.

15.

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
16.

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.

17.

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
18.

"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.

19.

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.

20.

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.

21.

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
22.

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.

23.

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.

24.

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.

25.

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.

26.

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
27.

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
28.

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.

29.

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
30.

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.

31.

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
32.

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.

33.

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.

34.

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
35.

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
36.

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
37.

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.

38.

Optimization of purification method and characterization of recombinant human Centrin-1.

Phanindranath R, Sudhakar DV, Sharma AK, Thangaraj K, Sharma Y.

Protein Expr Purif. 2016 Aug;124:48-54. doi: 10.1016/j.pep.2016.05.012. Epub 2016 May 24.

PMID:
27235176
39.

Corrigendum: Genetic affinities of the Jewish populations of India.

Chaubey G, Singh M, Rai N, Kariappa M, Singh K, Singh A, Singh DP, Tamang R, Rani DS, Reddy AG, Singh VK, Singh L, Thangaraj K.

Sci Rep. 2016 May 23;6:26421. doi: 10.1038/srep26421. No abstract available.

40.

Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.

Carlus SJ, Sarkar S, Bansal SK, Singh V, Singh K, Jha RK, Sadasivam N, Sadasivam SR, Gireesha PS, Thangaraj K, Rajender S.

PLoS One. 2016 Mar 16;11(3):e0151510. doi: 10.1371/journal.pone.0151510. eCollection 2016.

41.

Reply to 'Lack of replication of association of THSD7A with obesity'.

Nizamuddin S, Govindaraj P, Saxena S, Kashyap M, Mishra A, Singh S, Rotti H, Raval R, Nayak J, Bhat BK, Prasanna BV, Dhumal VR, Bhale S, Joshi KS, Dedge AP, Bharadwaj R, Gangadharan GG, Nair S, Gopinath PM, Patwardhan B, Kondaiah P, Satyamoorthy K, Valiathan MS, Thangaraj K.

Int J Obes (Lond). 2016 Apr;40(4):727-8. doi: 10.1038/ijo.2016.16. Epub 2016 Feb 2. No abstract available.

PMID:
26902698
42.

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.

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

Mitochondrion. 2016 Mar;27:1-5. doi: 10.1016/j.mito.2015.12.009. Epub 2016 Jan 4.

PMID:
26762927
43.

Genetic affinities of the Jewish populations of India.

Chaubey G, Singh M, Rai N, Kariappa M, Singh K, Singh A, Pratap Singh D, Tamang R, Selvi Rani D, Reddy AG, Kumar Singh V, Singh L, Thangaraj K.

Sci Rep. 2016 Jan 13;6:19166. doi: 10.1038/srep19166. Erratum in: Sci Rep. 2016 May 23;6:26421.

44.

Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup.

Singh S, Singh A, Rajkumar R, Sampath Kumar K, Kadarkarai Samy S, Nizamuddin S, Singh A, Ahmed Sheikh S, Peddada V, Khanna V, Veeraiah P, Pandit A, Chaubey G, Singh L, Thangaraj K.

Sci Rep. 2016 Jan 12;6:19157. doi: 10.1038/srep19157.

45.

Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.

Paramasivam A, Meena AK, Pedaparthi L, Jyothi V, Uppin MS, Jabeen SA, Sundaram C, Thangaraj K.

Mitochondrion. 2016 Jan;26:81-5. doi: 10.1016/j.mito.2015.12.006. Epub 2015 Dec 12.

PMID:
26689116
46.

Clinical, cytogenetic and molecular analysis of androgen insensitivity syndromes from south Indian cohort and detection and in-silico characterization of androgen receptor gene mutations.

V G A, S R, K M M, K T, S A, S N, A MP, J M, D A.

Clin Chim Acta. 2016 Jan 30;453:123-30. doi: 10.1016/j.cca.2015.12.012. Epub 2015 Dec 11.

PMID:
26688387
47.

Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.

Ali A, Qureshi SF, Medikare V, Venkateshwari A, Calambur N, Rao H, Jayakrishnan MP, Shenthar J, Thangaraj K, Nallari P.

J Interv Card Electrophysiol. 2016 Mar;45(2):119-30. doi: 10.1007/s10840-015-0082-5. Epub 2015 Dec 16.

PMID:
26670457
48.

Genome-wide analysis correlates Ayurveda Prakriti.

Govindaraj P, Nizamuddin S, Sharath A, Jyothi V, Rotti H, Raval R, Nayak J, Bhat BK, Prasanna BV, Shintre P, Sule M, Joshi KS, Dedge AP, Bharadwaj R, Gangadharan GG, Nair S, Gopinath PM, Patwardhan B, Kondaiah P, Satyamoorthy K, Valiathan MV, Thangaraj K.

Sci Rep. 2015 Oct 29;5:15786. doi: 10.1038/srep15786.

49.

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 Feb;61(2):167-72. doi: 10.1038/jhg.2015.121. Epub 2015 Oct 29.

PMID:
26511066
50.

Mutational analysis of SCN5A gene in long QT syndrome.

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

Meta Gene. 2015 Sep 2;6:26-35. doi: 10.1016/j.mgene.2015.07.010. eCollection 2015 Dec.

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