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Items: 42

1.

Nanoparticles in Pancreatic Cancer Imaging and Therapy.

Lakkakula S, Chalikonda G, Lakkakula BVKS.

Crit Rev Oncog. 2019;24(2):139-148. doi: 10.1615/CritRevOncog.2019031519.

PMID:
31679209
2.

DNA Fingerprint Technology: Its Application in Detecting Pancreatic Cancer.

Chalikonda G, Merchant N, Lakkakula BVKS, Nagaraju GP.

Crit Rev Oncog. 2019;24(2):133-137. doi: 10.1615/CritRevOncog.2019031603.

PMID:
31679208
3.

Engineered nanoparticles for imaging and drug delivery in colorectal cancer.

Pavitra E, Dariya B, Srivani G, Kang SM, Alam A, Sudhir PR, Kamal MA, Raju GSR, Han YK, Lakkakula BVKS, Nagaraju GP, Huh YS.

Semin Cancer Biol. 2019 Jun 29. pii: S1044-579X(19)30124-5. doi: 10.1016/j.semcancer.2019.06.017. [Epub ahead of print] Review.

PMID:
31260733
4.

Association between MTHFR 677C>T polymorphism and vascular complications in sickle cell disease: A meta-analysis.

Lakkakula BVKS.

Transfus Clin Biol. 2019 Nov;26(4):284-288. doi: 10.1016/j.tracli.2019.01.003. Epub 2019 Jan 10.

PMID:
30686687
5.

Small molecule tyrosine kinase inhibitors and pancreatic cancer-Trials and troubles.

Lakkakula BVKS, Farran B, Lakkakula S, Peela S, Yarla NS, Bramhachari PV, Kamal MA, Saddala MS, Nagaraju GP.

Semin Cancer Biol. 2019 Jun;56:149-167. doi: 10.1016/j.semcancer.2018.09.011. Epub 2018 Oct 9. Review.

PMID:
30314681
6.

Molecular docking analysis of phytoconstituent from Momordica charantia with Guanylate Cyclase catalytic domain.

Ghanta M, Panchanathan E, Lakkakula BVKS, Narayanaswamy A, Abhinand PA, Antony S.

Bioinformation. 2018 Jul 31;14(7):378-383. doi: 10.6026/97320630014378. eCollection 2018.

7.

Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.

Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.

Hemoglobin. 2018 Mar;42(2):84-90. doi: 10.1080/03630269.2018.1483946.

PMID:
30200838
8.

Pain Management Issues as Part of the Comprehensive Care of Patients with Sickle Cell Disease.

Lakkakula BVKS, Sahoo R, Verma H, Lakkakula S.

Pain Manag Nurs. 2018 Dec;19(6):558-572. doi: 10.1016/j.pmn.2018.06.004. Epub 2018 Jul 31. Review.

PMID:
30076112
9.

Relationship between matrilin-1 gene polymorphisms and mandibular retrognathism.

Balkhande PB, Lakkakula BVKS, Chitharanjan AB.

Am J Orthod Dentofacial Orthop. 2018 Feb;153(2):255-261.e1. doi: 10.1016/j.ajodo.2017.06.023.

PMID:
29407503
10.

Cyclic Guanosine Monophosphate-Dependent Protein Kinase I Stimulators and Activators Are Therapeutic Alternatives for Sickle Cell Disease.

Ghanta M, Panchanathan E, Lakkakula BV.

Turk J Haematol. 2018 Mar 1;35(1):77-78. doi: 10.4274/tjh.2017.0407. Epub 2017 Dec 1. No abstract available.

11.

Retrospection on the Role of Soluble Guanylate Cyclase in Parkinson's Disease.

Ghanta M, Panchanathan E, Lakkakula BVKS, Narayanaswamy A.

J Pharmacol Pharmacother. 2017 Jul-Sep;8(3):87-91. doi: 10.4103/jpp.JPP_45_17. Review.

12.

Transmission analysis of TGFB1 gene polymorphisms in non-syndromic cleft lip with or without cleft palate.

Raju GT, Lakkakula BVKS, Murthy J, Kannan MA, Paul SFD.

Int J Pediatr Otorhinolaryngol. 2017 Sep;100:14-17. doi: 10.1016/j.ijporl.2017.06.015. Epub 2017 Jun 16.

PMID:
28802359
13.

IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population.

Gurramkonda VB, Syed AH, Murthy J, Lakkakula BVKS.

Braz J Otorhinolaryngol. 2018 Jul - Aug;84(4):473-477. doi: 10.1016/j.bjorl.2017.05.011. Epub 2017 Jun 26.

14.

Presence of atypical beta globin (HBB) gene cluster haplotypes in sickle cell anemia patients of India.

Nongbri SRL, Verma HK, Lakkakula BVKS, Patra PK.

Rev Bras Hematol Hemoter. 2017 Apr - Jun;39(2):180-182. doi: 10.1016/j.bjhh.2017.01.007. Epub 2017 Feb 27. No abstract available.

15.

Aldosterone synthase gene is not a major susceptibility gene for progression of chronic kidney disease in patients with autosomal dominant polycystic kidney disease.

Ramanathan G, Elumalai R, Periyasamy S, Lakkakula BVKS.

Saudi J Kidney Dis Transpl. 2017 May-Jun;28(3):552-557. doi: 10.4103/1319-2442.206464.

16.

Assessment of renal function in Indian patients with sickle cell disease.

Lakkakula BVKS, Verma HK, Choubey M, Patra S, Khodiar PK, Patra PK.

Saudi J Kidney Dis Transpl. 2017 May-Jun;28(3):524-531. doi: 10.4103/1319-2442.206440.

17.

Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India.

Chawla S, Singh RK, Lakkakula BVKS, Vadlamudi RR.

J Community Genet. 2017 Jul;8(3):159-166. doi: 10.1007/s12687-017-0298-4. Epub 2017 Apr 6.

18.

Clinical Relevance of Cytokines Gene Polymorphisms and Protein Levels in Gingival Cervical Fluid from Chronic Periodontitis Patients.

Lavu V, Venkatesan V, Venugopal P, Lakkakula BV, Paul SF, Peria K, Rao SR.

Iran J Immunol. 2017 Mar;14(1):51-58. doi: IJIv14i1A5.

19.

Influence of angiotensin converting enzyme (ACE) gene rs4362 polymorphism on the progression of kidney failure in patients with autosomal dominant polycystic kidney disease (ADPKD).

Ramanathan G, Ghosh S, Elumalai R, Periyasamy S, Lakkakula BV.

Indian J Med Res. 2016 Jun;143(6):748-755. doi: 10.4103/0971-5916.191992.

20.

Role of myosin 1H gene polymorphisms in mandibular retrognathism.

Arun RM, Lakkakula BV, Chitharanjan AB.

Am J Orthod Dentofacial Orthop. 2016 May;149(5):699-704. doi: 10.1016/j.ajodo.2015.10.028.

PMID:
27131252
21.

Renin gene rs1464816 polymorphism contributes to chronic kidney disease progression in ADPKD.

Ramanathan G, Elumalai R, Periyasamy S, Lakkakula BV.

J Biomed Sci. 2016 Jan 11;23:1. doi: 10.1186/s12929-015-0217-0.

22.

Endothelin 1 gene is not a major modifier of chronic kidney disease advancement among the autosomal dominant polycystic kidney disease patients.

Annapareddy SN, Elumalai R, Lakkakula BV, Ramanathan G, Periyasamy S.

J Nephropharmacol. 2015 Dec 9;5(1):13-18. eCollection 2016.

23.

SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population.

Gurramkonda VB, Syed AH, Murthy J, Lakkakula BV.

J Oral Biol Craniofac Res. 2015 Sep-Dec;5(3):161-4. doi: 10.1016/j.jobcr.2015.06.014. Epub 2015 Jul 29.

24.

Angiotensinogen gene polymorphisms and progression of chronic kidney disease in ADPKD patients.

Gnanasambandan R, Elumalai R, Soundararajan P, Lakkakula BVKS.

Clin Exp Nephrol. 2016 Aug;20(4):561-568. doi: 10.1007/s10157-015-1183-2. Epub 2015 Oct 19.

PMID:
26482465
25.

Evidence of the involvement of the polymorphisms near MSX1 gene in non-syndromic cleft lip with or without cleft palate.

Gurramkonda VB, Syed AH, Murthy J, Lakkakula BV.

Int J Pediatr Otorhinolaryngol. 2015 Jul;79(7):1081-4. doi: 10.1016/j.ijporl.2015.04.034. Epub 2015 Apr 29.

PMID:
25953455
26.

Two promoter polymorphisms in TBX22 are associated with the risk of NSCLP in Indian women.

Gurramkonda VB, Hussain SA, Murthy J, Lakkakula BV.

Clin Dysmorphol. 2015 Oct;24(4):140-3. doi: 10.1097/MCD.0000000000000088.

PMID:
25918826
27.

Role of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney disease.

Elumalai R, Periasamy S, Ramanathan G, Lakkakula BV.

J Renal Inj Prev. 2014 Jul 1;3(3):69-73. doi: 10.12861/jrip.2014.21. eCollection 2014.

28.

Significant association of MTHFD1 1958G>A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population.

Murthy J, Gurramkonda VB, Lakkakula BV.

Med Oral Patol Oral Cir Bucal. 2014 Nov 1;19(6):e616-21.

29.

NOS3 tagSNPs does not modify the chronic kidney disease progression in autosomal dominant polycystic kidney disease.

Ramanathan G, Periyasamy S, Lakkakula BV.

Nephrology (Carlton). 2014 Sep;19(9):537-41. doi: 10.1111/nep.12278.

PMID:
24824375
30.

CBS c.844ins68 Polymorphism Frequencies in Control Populations: Implications on Nonsyndromic Cleft Lip With or Without Cleft Palate.

Murthy J, Lakkakula S, Gurramkonda VB, Pathapati RM, Maram R, Lakkakula BV.

Cleft Palate Craniofac J. 2015 Jan;52(1):49-53. doi: 10.1597/13-051.

PMID:
24437588
31.

MTHFR C677T and A1298C polymorphisms and risk of nonsyndromic orofacial clefts in a south Indian population.

Murthy J, Gurramkonda VB, Karthik N, Lakkakula BV.

Int J Pediatr Otorhinolaryngol. 2014 Feb;78(2):339-42. doi: 10.1016/j.ijporl.2013.12.005. Epub 2013 Dec 13.

PMID:
24380661
32.

Effect of flupirtine on the growth and viability of U373 malignant glioma cells.

Panchanathan E, Ramanathan G, Lakkakula BV.

Cancer Biol Med. 2013 Sep;10(3):142-7. doi: 10.7497/j.issn.2095-3941.2013.03.004.

33.

NAT2 genetic variations among South Indian populations.

Lakkakula S, Mohan Pathapati R, Chaubey G, Munirajan AK, Lakkakula BV, Maram R.

Hum Genome Var. 2014 Oct 2;1:14014. doi: 10.1038/hgv.2014.14. eCollection 2014.

34.

Genetic variants associated with insulin signaling and glucose homeostasis in the pathogenesis of insulin resistance in polycystic ovary syndrome: a systematic review.

Lakkakula BV, Thangavelu M, Godla UR.

J Assist Reprod Genet. 2013 Jul;30(7):883-95. doi: 10.1007/s10815-013-0030-1. Epub 2013 Jun 22. Review.

35.

Functional PstI/RsaI polymorphisms in the CYP2E1 gene among south Indian populations.

Lakkakula S, Maram R, Munirajan AK, Pathapati RM, Visveswara SB, Lakkakula BV.

Asian Pac J Cancer Prev. 2013;14(1):179-82.

36.

HLA class II SNP interactions and the association with type 1 diabetes mellitus in Bengali speaking patients of Eastern India.

Raha O, Sarkar B, Lakkakula BV, Pasumarthy V, Godi S, Chowdhury S, Raychaudhuri P, Vadlamudi RR.

J Biomed Sci. 2013 Feb 27;20:12. doi: 10.1186/1423-0127-20-12.

37.

Molecular basis of β-thalassemia in Karnataka, India.

Kulkarni GD, Kulkarni SS, Kadakol GS, Kulkarni BB, Kyamangoudar PH, Lakkakula BV, Thangaraj K, Shepur TA, Kulkarni ML, Gai PB.

Genet Test Mol Biomarkers. 2012 Feb;16(2):138-41. doi: 10.1089/gtmb.2011.0035. Epub 2011 Oct 6.

PMID:
21978377
38.

Apelin gene polymorphism influences apelin expression and obesity phenotypes in Chinese women.

Liao YC, Chou WW, Li YN, Chuang SC, Lin WY, Lakkakula BV, Yu ML, Juo SH.

Am J Clin Nutr. 2011 Sep;94(3):921-8. doi: 10.3945/ajcn.110.008813. Epub 2011 Jul 20.

PMID:
21775567
39.

Lack of association of EPHX1 genotypes and haplotypes with oral cancer in South Indians.

Balaji L, Lakkakula BV, Krishna BS, Paul SF.

Genet Test Mol Biomarkers. 2011 Sep;15(9):595-9. doi: 10.1089/gtmb.2010.0260. Epub 2011 Mar 31.

PMID:
21453055
40.

A novel polymorphism in codon 25 of the KRAS gene associated with gallbladder carcinoma patients of the eastern part of India.

Pramanik V, Sarkar BN, Kar M, Das G, Malay BK, Sufia KK, Lakkakula BV, Vadlamudi RR.

Genet Test Mol Biomarkers. 2011 Jun;15(6):431-4. doi: 10.1089/gtmb.2010.0194. Epub 2011 Mar 4.

PMID:
21375404
41.

Lack of association between the IL-10 gene polymorphisms and features of the metabolic syndrome.

Lu MY, Lakkakula BV, Liao YC, Tsai PC, Yang YH, Juo SH.

J Investig Med. 2011 Feb;59(2):267-71. doi: 10.2310/JIM.0b013e3182050a36.

PMID:
21328800
42.

Association between the M268T polymorphism in the angiotensinogen gene and essential hypertension in a South Indian population.

Gopi Chand M, Srinath J, Rao RS, Lakkakula BV, Kumar S, Rao VR.

Biochem Genet. 2011 Aug;49(7-8):474-82. doi: 10.1007/s10528-011-9423-y. Epub 2011 Feb 11.

PMID:
21312059

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