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Items: 46

1.

Making NSC and Neurons from Patient-Derived Tissue Samples.

Mukherjee O, Acharya S, Rao M.

Methods Mol Biol. 2019;1919:9-24. doi: 10.1007/978-1-4939-9007-8_2.

PMID:
30656618
2.

INDEX-db: The Indian Exome Reference Database (Phase I).

Ahmed P H, V V, More RP, Viswanath B, Jain S, Rao MS, Mukherjee O; ADBS Consortium.

J Comput Biol. 2019 Mar;26(3):225-234. doi: 10.1089/cmb.2018.0199. Epub 2019 Jan 7.

3.

Derivation of iPSC lines from two patients with familial Alzheimer's disease from India.

Najar AH, Sneha KM, Ashok A, Babu S, Subramaniam AG, Kannan R, Viswanath B, Purushottam M, Varghese M, Parvez S, Panicker MM, Mukherjee O, Jain S.

Stem Cell Res. 2019 Jan;34:101370. doi: 10.1016/j.scr.2018.101370. Epub 2018 Dec 19.

4.

Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.

Ganesh S, Ahmed P H, Nadella RK, More RP, Seshadri M, Viswanath B, Rao M, Jain S; ADBS Consortium, Mukherjee O.

Psychiatry Clin Neurosci. 2019 Jan;73(1):11-19. doi: 10.1111/pcn.12788. Epub 2018 Dec 12.

PMID:
30367527
5.

Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A).

Kumar D, Hussain A, Srivastava AK, Mukerji M, Mukherjee O, Faruq M.

Stem Cell Res. 2018 Aug;31:216-221. doi: 10.1016/j.scr.2018.08.008. Epub 2018 Aug 14.

6.

Developing two reference control samples for the Indian population.

Iyer S, Bhatia P, Rao M, Mukherjee O.

Stem Cell Res. 2018 Jul;30:38-42. doi: 10.1016/j.scr.2018.05.001. Epub 2018 May 12.

7.

Discovery biology of neuropsychiatric syndromes (DBNS): a center for integrating clinical medicine and basic science.

Viswanath B, Rao NP, Narayanaswamy JC, Sivakumar PT, Kandasamy A, Kesavan M, Mehta UM, Venkatasubramanian G, John JP, Mukherjee O, Purushottam M, Kannan R, Mehta B, Kandavel T, Binukumar B, Saini J, Jayarajan D, Shyamsundar A, Moirangthem S, Vijay Kumar KG, Thirthalli J, Chandra PS, Gangadhar BN, Murthy P, Panicker MM, Bhalla US, Chattarji S, Benegal V, Varghese M, Reddy JYC, Raghu P, Rao M, Jain S.

BMC Psychiatry. 2018 Apr 18;18(1):106. doi: 10.1186/s12888-018-1674-2.

8.

Mutation burden profile in familial Alzheimer's disease cases from India.

Syama A, Sen S, Kota LN, Viswanath B, Purushottam M, Varghese M, Jain S, Panicker MM, Mukherjee O.

Neurobiol Aging. 2018 Apr;64:158.e7-158.e13. doi: 10.1016/j.neurobiolaging.2017.12.002. Epub 2017 Dec 12.

PMID:
29329714
9.

Effect of CLU and PICALM polymorphisms on AD risk: A study from south India.

Shankarappa BM, Kota LN, Purushottam M, Nagpal K, Mukherjee O, Viswanath B, Varghese M, Bharath S, Jain S.

Asian J Psychiatr. 2017 Jun;27:7-11. doi: 10.1016/j.ajp.2016.12.017. Epub 2016 Dec 29.

PMID:
28558900
10.

Genotoxic Effects of Culture Media on Human Pluripotent Stem Cells.

Prakash Bangalore M, Adhikarla S, Mukherjee O, Panicker MM.

Sci Rep. 2017 Feb 8;7:42222. doi: 10.1038/srep42222.

11.

Adherence to Intestinal Cells Promotes Biofilm Formation in Vibrio cholerae.

Sengupta C, Mukherjee O, Chowdhury R.

J Infect Dis. 2016 Nov 15;214(10):1571-1578. Epub 2016 Sep 16.

PMID:
27638940
12.

A Method to Identify and Isolate Pluripotent Human Stem Cells and Mouse Epiblast Stem Cells Using Lipid Body-Associated Retinyl Ester Fluorescence.

Muthusamy T, Mukherjee O, Menon R, Prakash Bangalore M, Panicker MM.

Stem Cell Reports. 2016 Aug 9;7(2):306. doi: 10.1016/j.stemcr.2016.07.023. No abstract available.

13.

Detailed Characterization of Human Induced Pluripotent Stem Cells Manufactured for Therapeutic Applications.

Baghbaderani BA, Syama A, Sivapatham R, Pei Y, Mukherjee O, Fellner T, Zeng X, Rao MS.

Stem Cell Rev Rep. 2016 Aug;12(4):394-420. doi: 10.1007/s12015-016-9662-8.

14.

Moonlighting of Helicobacter pylori catalase protects against complement-mediated killing by utilising the host molecule vitronectin.

Richter C, Mukherjee O, Ermert D, Singh B, Su YC, Agarwal V, Blom AM, Riesbeck K.

Sci Rep. 2016 Apr 18;6:24391. doi: 10.1038/srep24391.

15.

A Conserved Helicobacter pylori Gene, HP0102, Is Induced Upon Contact With Gastric Cells and Has Multiple Roles in Pathogenicity.

Bhattacharya S, Mukherjee O, Mukhopadhyay AK, Chowdhury R, Pal AK, Dhar KK.

J Infect Dis. 2016 Jul 15;214(2):196-204. doi: 10.1093/infdis/jiw139. Epub 2016 Apr 7. Erratum in: J Infect Dis. 2016 Oct 1;214(7):1127.

PMID:
27056952
16.

Haemophilus influenzae Type f Hijacks Vitronectin Using Protein H To Resist Host Innate Immunity and Adhere to Pulmonary Epithelial Cells.

Al-Jubair T, Mukherjee O, Oosterhuis S, Singh B, Su YC, Fleury C, Blom AM, Törnroth-Horsefield S, Riesbeck K.

J Immunol. 2015 Dec 15;195(12):5688-95. doi: 10.4049/jimmunol.1501197. Epub 2015 Nov 4.

17.

C9orf72 mutations may be rare in frontotemporal lobar degeneration patients in India.

Mukherjee O, Das G, Sen S, Dutt A, Alladi S, Ghosh A.

Amyotroph Lateral Scler Frontotemporal Degener. 2015;17(1-2):151-3. doi: 10.3109/21678421.2015.1074706. Epub 2015 Oct 14. No abstract available.

PMID:
26465714
18.

Haemophilus influenzae P4 Interacts With Extracellular Matrix Proteins Promoting Adhesion and Serum Resistance.

Su YC, Mukherjee O, Singh B, Hallgren O, Westergren-Thorsson G, Hood D, Riesbeck K.

J Infect Dis. 2016 Jan 15;213(2):314-23. doi: 10.1093/infdis/jiv374. Epub 2015 Jul 7.

19.

Moraxella catarrhalis Binds Plasminogen To Evade Host Innate Immunity.

Singh B, Al-Jubair T, Voraganti C, Andersson T, Mukherjee O, Su YC, Zipfel P, Riesbeck K.

Infect Immun. 2015 Sep;83(9):3458-69. doi: 10.1128/IAI.00310-15. Epub 2015 Jun 22.

20.

Cellular models to study bipolar disorder: A systematic review.

Viswanath B, Jose SP, Squassina A, Thirthalli J, Purushottam M, Mukherjee O, Vladimirov V, Patrinos GP, Del Zompo M, Jain S.

J Affect Disord. 2015 Sep 15;184:36-50. doi: 10.1016/j.jad.2015.05.037. Epub 2015 May 28. Review.

PMID:
26070045
21.

A fusion protein derived from Moraxella catarrhalis and Neisseria meningitidis aimed for immune modulation of human B cells.

Mukherjee O, Singh B, Bayrak B, Jonsson AB, Mörgelin M, Riesbeck K.

Hum Vaccin Immunother. 2015;11(9):2223-7. doi: 10.1080/21645515.2015.1034917. Epub 2015 Jun 4.

22.

A method to identify and isolate pluripotent human stem cells and mouse epiblast stem cells using lipid body-associated retinyl ester fluorescence.

Muthusamy T, Mukherjee O, Menon R, Megha PB, Panicker MM.

Stem Cell Reports. 2014 Jun 12;3(1):169-84. doi: 10.1016/j.stemcr.2014.05.004. eCollection 2014 Jul 8. Erratum in: Stem Cell Reports. 2016 Aug 9;7(2):306.

23.

A fine-tuned interaction between trimeric autotransporter haemophilus surface fibrils and vitronectin leads to serum resistance and adherence to respiratory epithelial cells.

Singh B, Su YC, Al-Jubair T, Mukherjee O, Hallström T, Mörgelin M, Blom AM, Riesbeck K.

Infect Immun. 2014 Jun;82(6):2378-89. doi: 10.1128/IAI.01636-13. Epub 2014 Mar 24.

24.

Dual phosphorylation of cdk1 coordinates cell proliferation with key developmental processes in Drosophila.

Ayeni JO, Varadarajan R, Mukherjee O, Stuart DT, Sprenger F, Srayko M, Campbell SD.

Genetics. 2014 Jan;196(1):197-210. doi: 10.1534/genetics.113.156281. Epub 2013 Nov 8.

25.

Next generation therapy in chronic myeloid leukemia.

Bhattacharya PK, Bhattacharya U, Bhattacharya R, Bhattacharya R, Bhattacharya S, Bhattacharya R, Mukherjee D, Mukherjee O, Mukherjee D, Barman DR, Das S, Dey A, Biswas RR, Sarkar S.

Indian J Hematol Blood Transfus. 2012 Sep;28(3):189-90. doi: 10.1007/s12288-011-0139-2. Epub 2012 Apr 8. No abstract available.

26.

Apolipoprotein E4 and brain white matter integrity in Alzheimer's disease: tract-based spatial statistics study under 3-Tesla MRI.

Bagepally BS, Halahalli HN, John JP, Kota L, Purushottam M, Mukherjee O, Sivakumar PT, Bharath S, Jain S, Varghese M.

Neurodegener Dis. 2012;10(1-4):145-8. doi: 10.1159/000334761. Epub 2012 Jan 21.

PMID:
22269984
27.

ApoE4 and late onset depression in Indian population.

Sureshkumar R, Bharath S, Jain S, Prakash O, Purushottam M, Thennarasu K, Mukherjee O, Sivakumar PT, Varghese M.

J Affect Disord. 2012 Feb;136(3):244-8. doi: 10.1016/j.jad.2011.12.022. Epub 2012 Jan 5.

PMID:
22226379
28.

The SH2-domain of SHIP1 interacts with the SHIP1 C-terminus: impact on SHIP1/Ig-α interaction.

Mukherjee O, Weingarten L, Padberg I, Pracht C, Sinha R, Hochdörfer T, Kuppig S, Backofen R, Reth M, Huber M.

Biochim Biophys Acta. 2012 Feb;1823(2):206-14. doi: 10.1016/j.bbamcr.2011.11.019. Epub 2011 Dec 13.

29.

Apolipoprotein E polymorphism and dementia: a hospital-based study from southern India.

Bharath S, Purushottam M, Mukherjee O, Bagepally BS, Prakash O, Kota L, Krishnappa SB, Sivakumar PT, Jain S, Varghese M.

Dement Geriatr Cogn Disord. 2010;30(6):455-60. doi: 10.1159/000322093. Epub 2011 Jan 20.

30.

Genetic polymorphism in the serotonin transporter promoter region and ecological success in macaques.

Chakraborty S, Chakraborty D, Mukherjee O, Jain S, Ramakrishnan U, Sinha A.

Behav Genet. 2010 Sep;40(5):672-9. doi: 10.1007/s10519-010-9360-2. Epub 2010 Apr 22.

PMID:
20411319
31.

North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion.

Singh I, Faruq M, Mukherjee O, Jain S, Pal PK, Srivastav MV, Behari M, Srivastava AK, Mukerji M.

Ann Hum Genet. 2010 May;74(3):202-10. doi: 10.1111/j.1469-1809.2010.00569.x. Epub 2010 Mar 31.

32.

Phylogenetic analysis and selection pressures of 5-HT receptors in human and non-human primates: receptor of an ancient neurotransmitter.

Anbazhagan P, Purushottam M, Kumar HB, Mukherjee O, Jain S, Sowdhamini R.

J Biomol Struct Dyn. 2010 Apr;27(5):581-98. Erratum in: J Biomol Struct Dyn. 2010 Jun;27(6):890.

PMID:
20085376
33.

Evaluating epistatic interaction signals in complex traits using quantitative traits.

Mukherjee O, Sanapala KR, Anbazhagana P, Ghosh S.

BMC Proc. 2009 Dec 15;3 Suppl 7:S82.

34.

The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16.

An P, Mukherjee O, Chanda P, Yao L, Engelman CD, Huang CH, Zheng T, Kovac IP, Dubé MP, Liang X, Li J, de Andrade M, Culverhouse R, Malzahn D, Manning AK, Clarke GM, Jung J, Province MA.

Genet Epidemiol. 2009;33 Suppl 1:S58-67. doi: 10.1002/gepi.20474.

35.

Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment.

Gupta M, Bhatnagar P, Grover S, Kaur H, Baghel R, Bhasin Y, Chauhan C, Verma B, Manduva V, Mukherjee O, Purushottam M, Sharma A, Jain S, Brahmachari SK, Kukreti R.

Pharmacogenomics. 2009 Mar;10(3):385-97. doi: 10.2217/14622416.10.3.385.

PMID:
19290789
36.

Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms.

Gupta M, Chauhan C, Bhatnagar P, Gupta S, Grover S, Singh PK, Purushottam M, Mukherjee O, Jain S, Brahmachari SK, Kukreti R.

Pharmacogenomics. 2009 Feb;10(2):277-91. doi: 10.2217/14622416.10.2.277.

PMID:
19207030
37.

Evolutionary analysis of PHLPP1 gene in humans and non-human primates.

Anbazhagan P, Purushottam M, Kumar HB, Kubendran S, Mukherjee O, Brahmachari SK, Jain S, Sowdhamini R.

Bioinformation. 2008 Aug 1;2(10):471-4.

38.

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia.

Mukherjee O, Wang J, Gitcho M, Chakraverty S, Taylor-Reinwald L, Shears S, Kauwe JS, Norton J, Levitch D, Bigio EH, Hatanpaa KJ, White CL, Morris JC, Cairns NJ, Goate A.

Hum Mutat. 2008 Apr;29(4):512-21. doi: 10.1002/humu.20681.

39.

Serotonergic candidate genes and puerperal psychosis: an association study.

Kumar HB, Purushottam M, Kubendran S, Gayathri P, Mukherjee O, Murthy AR, Ghosh S, Chandra P, Reddy YC, Benegal V, Brahmachari SK, Jain S.

Psychiatr Genet. 2007 Oct;17(5):253-60. Erratum in: Psychiatr Genet. 2007 Dec;17(6):360.

PMID:
17728663
40.

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes.

Schymick JC, Yang Y, Andersen PM, Vonsattel JP, Greenway M, Momeni P, Elder J, Chiò A, Restagno G, Robberecht W, Dahlberg C, Mukherjee O, Goate A, Graff-Radford N, Caselli RJ, Hutton M, Gass J, Cannon A, Rademakers R, Singleton AB, Hardiman O, Rothstein J, Hardy J, Traynor BJ.

J Neurol Neurosurg Psychiatry. 2007 Jul;78(7):754-6. Epub 2007 Mar 19.

41.

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

Behrens MI, Mukherjee O, Tu PH, Liscic RM, Grinberg LT, Carter D, Paulsmeyer K, Taylor-Reinwald L, Gitcho M, Norton JB, Chakraverty S, Goate AM, Morris JC, Cairns NJ.

Alzheimer Dis Assoc Disord. 2007 Jan-Mar;21(1):1-7.

PMID:
17334266
42.

Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease.

Mukherjee O, Kauwe JS, Mayo K, Morris JC, Goate AM.

BMC Genet. 2007 Jan 31;8:3.

43.

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin.

Mukherjee O, Pastor P, Cairns NJ, Chakraverty S, Kauwe JS, Shears S, Behrens MI, Budde J, Hinrichs AL, Norton J, Levitch D, Taylor-Reinwald L, Gitcho M, Tu PH, Tenenholz Grinberg L, Liscic RM, Armendariz J, Morris JC, Goate AM.

Ann Neurol. 2006 Sep;60(3):314-22.

44.

Evidence of linkage and association on 18p11.2 for psychosis.

Mukherjee O, Meera P, Ghosh S, Kubendran S, Kiran K, Manjunath KR, Subhash MN, Benegal V, Brahmachari SK, Majumder PP, Jain S.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):868-73.

PMID:
16941653
45.

Common psychiatric diseases and human genetic variation.

Mukherjee O, Saleem Q, Purushottam M, Anand A, Brahmachari SK, Jain S.

Community Genet. 2002;5(3):171-7.

PMID:
14960887
46.

Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder.

Saleem Q, Dash D, Gandhi C, Kishore A, Benegal V, Sherrin T, Mukherjee O, Jain S, Brahmachari SK.

Mol Psychiatry. 2001 Nov;6(6):694-700.

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