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Items: 1 to 50 of 943

1.

Access to Services in Rural Areas from the Point of View of Older Population-A Case Study in Finland.

Verma I, Taegen J.

Int J Environ Res Public Health. 2019 Dec 2;16(23). pii: E4854. doi: 10.3390/ijerph16234854.

2.

Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation.

Arora V, Bijarnia-Mahay S, Kulshreshtra S, Singh K, Puri RD, Verma IC.

Autops Case Rep. 2019 Sep 30;9(4):e2019124. doi: 10.4322/acr.2019.124. eCollection 2019 Oct-Dec.

3.

Clinical and Molecular Disease Spectrum and Outcomes in Patients with Infantile-Onset Pompe Disease.

Gupta N, Kazi ZB, Nampoothiri S, Jagdeesh S, Kabra M, Puri RD, Muranjan M, Kalaivani M, Rehder C, Bali D, Verma IC, Kishnani PS.

J Pediatr. 2020 Jan;216:44-50.e5. doi: 10.1016/j.jpeds.2019.08.058. Epub 2019 Oct 9.

PMID:
31606152
4.

Successful Derivation of an Induced Pluripotent Stem Cell Line from a Genetically Nonpermissive Enhanced Green Fluorescent Protein-Transgenic FVB/N Mouse Strain.

Abbey D, Singh G, Verma I, Derebail S, Kolkundkar U, Chandrashekar DS, Acharya KK, Vemuri MC, Seshagiri PB.

Cell Reprogram. 2019 Oct;21(5):270-284. doi: 10.1089/cell.2019.0019.

PMID:
31596624
5.

Transcriptome analysis of the effect of GA3 in sugarcane culm.

Chandra A, Roopendra K, Verma I.

3 Biotech. 2019 Oct;9(10):376. doi: 10.1007/s13205-019-1908-0. Epub 2019 Sep 28.

PMID:
31588400
6.

Prevalence of Metabolic Syndrome in Rheumatoid Arthritis Patients: A Case Control Study from a Tertiary Care Centre in North India.

Naidu G, Bhilave N, Sharma K, Verma I, Sharma A.

J Assoc Physicians India. 2019 Jul;67(7):22-24.

PMID:
31559763
7.

Maternal hyperuricemia as a marker of post-spinal hypotension and uterine tone during cesarean delivery: a prospective observational study.

Bhatia N, Shanmugam R, Jain K, Sikka P, Verma I.

Arch Gynecol Obstet. 2019 Oct;300(4):925-931. doi: 10.1007/s00404-019-05282-x. Epub 2019 Sep 14.

PMID:
31520262
8.

Inborn Errors of Metabolism in India- Where We are At!

Bijarnia-Mahay S, Verma IC.

Indian J Pediatr. 2019 Oct;86(10):875-876. doi: 10.1007/s12098-019-03067-3. Epub 2019 Sep 10. No abstract available.

PMID:
31506781
9.

Transcriptional signatures of Mycobacterium tuberculosis in mouse model of intraocular tuberculosis.

Abhishek S, Ryndak MB, Choudhary A, Sharma S, Gupta A, Gupta V, Singh N, Laal S, Verma I.

Pathog Dis. 2019 Jul 1;77(5). pii: ftz045. doi: 10.1093/femspd/ftz045.

PMID:
31504463
10.

Co-inheritance of pathogenic variants in PKD1 and PKD2 genes presenting as severe antenatal phenotype of autosomal dominant polycystic kidney disease.

Arora V, Bijarnia-Mahay S, Tiwari V, Bansal S, Gupta P, Setia N, Puri RD, Verma IC.

Eur J Med Genet. 2019 Jul 23:103734. doi: 10.1016/j.ejmg.2019.103734. [Epub ahead of print]

PMID:
31349084
11.

An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma.

Neftel C, Laffy J, Filbin MG, Hara T, Shore ME, Rahme GJ, Richman AR, Silverbush D, Shaw ML, Hebert CM, Dewitt J, Gritsch S, Perez EM, Gonzalez Castro LN, Lan X, Druck N, Rodman C, Dionne D, Kaplan A, Bertalan MS, Small J, Pelton K, Becker S, Bonal D, Nguyen QD, Servis RL, Fung JM, Mylvaganam R, Mayr L, Gojo J, Haberler C, Geyeregger R, Czech T, Slavc I, Nahed BV, Curry WT, Carter BS, Wakimoto H, Brastianos PK, Batchelor TT, Stemmer-Rachamimov A, Martinez-Lage M, Frosch MP, Stamenkovic I, Riggi N, Rheinbay E, Monje M, Rozenblatt-Rosen O, Cahill DP, Patel AP, Hunter T, Verma IM, Ligon KL, Louis DN, Regev A, Bernstein BE, Tirosh I, Suvà ML.

Cell. 2019 Aug 8;178(4):835-849.e21. doi: 10.1016/j.cell.2019.06.024. Epub 2019 Jul 18.

PMID:
31327527
12.

Correction to "Liquid Crystal based Detection of Pb(II) Ions Using Spinach RNA as Recognition Probe".

Verma I, Devi M, Sharma D, Nandi R, Pal SK.

Langmuir. 2019 Jul 30;35(30):9994. doi: 10.1021/acs.langmuir.9b02053. Epub 2019 Jul 19. No abstract available.

PMID:
31322354
13.

Modeling Gliomas Using Two Recombinases.

Hara T, Verma IM.

Cancer Res. 2019 Aug 1;79(15):3983-3991. doi: 10.1158/0008-5472.CAN-19-0717. Epub 2019 Jul 17.

14.

A novel CHEK2 variant identified by next generation sequencing in an Indian family with hereditary breast cancer syndrome.

Bhai P, Saxena R, Kulshrestha S, Verma IC.

Cancer Genet. 2019 Jun;235-236:13-17. doi: 10.1016/j.cancergen.2019.05.003. Epub 2019 May 31.

PMID:
31296309
15.

Prevalence of familial hypercholesterolemia in premature coronary artery disease patients admitted to a tertiary care hospital in North India.

Sawhney JPS, Prasad SR, Sharma M, Madan K, Mohanty A, Passey R, Mehta A, Kandpal B, Makhija A, Jain R, Mantri RR, Vivek BS, Manchanda SC, Verma IC.

Indian Heart J. 2019 Mar - Apr;71(2):118-122. doi: 10.1016/j.ihj.2018.12.004. Epub 2019 Jan 3.

16.

Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases.

Murakami Y, Nguyen TTM, Baratang N, Raju PK, Knaus A, Ellard S, Jones G, Lace B, Rousseau J, Ajeawung NF, Kamei A, Minase G, Akasaka M, Araya N, Koshimizu E, van den Ende J, Erger F, Altmüller J, Krumina Z, Strautmanis J, Inashkina I, Stavusis J, El-Gharbawy A, Sebastian J, Puri RD, Kulshrestha S, Verma IC, Maier EM, Haack TB, Israni A, Baptista J, Gunning A, Rosenfeld JA, Liu P, Joosten M, Rocha ME, Hashem MO, Aldhalaan HM, Alkuraya FS, Miyatake S, Matsumoto N, Krawitz PM, Rossignol E, Kinoshita T, Campeau PM.

Am J Hum Genet. 2019 Aug 1;105(2):384-394. doi: 10.1016/j.ajhg.2019.05.019. Epub 2019 Jun 27.

PMID:
31256876
17.

Time varying causal network reconstruction of a mouse cell cycle.

Masnadi-Shirazi M, Maurya MR, Pao G, Ke E, Verma IM, Subramaniam S.

BMC Bioinformatics. 2019 May 29;20(1):294. doi: 10.1186/s12859-019-2895-1.

18.

Exploiting chitosan and gold nanoparticles for antimycobacterial activity of in silico identified antimicrobial motif of human neutrophil peptide-1.

Sharma R, Raghav R, Priyanka K, Rishi P, Sharma S, Srivastava S, Verma I.

Sci Rep. 2019 May 27;9(1):7866. doi: 10.1038/s41598-019-44256-6.

19.

Liquid Crystal based Detection of Pb(II) Ions Using Spinach RNA as Recognition Probe.

Verma I, Devi M, Sharma D, Nandi R, Pal SK.

Langmuir. 2019 Jun 18;35(24):7816-7823. doi: 10.1021/acs.langmuir.8b04018. Epub 2019 May 30. Erratum in: Langmuir. 2019 Jul 30;35(30):9994.

PMID:
31117720
20.

The fatal fetal tumor: a geneticist's perspective.

Arora V, Bijarnia Mahay S, Rao S, Dimri N, Manocha A, Mansukhani C, Mishra R, Gupta S, Dua Puri R, Verma IC.

J Matern Fetal Neonatal Med. 2019 Jun 3:1-3. doi: 10.1080/14767058.2019.1622671. [Epub ahead of print]

PMID:
31113261
21.

Cell culture conditions affect the ability of high content imaging assay to detect drug-induced changes in cellular parameters in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs).

Balasubramanian B, Belak V, Verma I, Prysiazhniuk Y, Sannajust F, Trepakova ES.

Toxicol Rep. 2019 Mar 28;6:305-320. doi: 10.1016/j.toxrep.2019.02.004. eCollection 2019.

22.

Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.

Khatter S, Puri RD, Mahay SB, Bhai P, Saxena R, Verma IC.

Indian J Dermatol. 2019 Mar-Apr;64(2):143-145. doi: 10.4103/ijd.IJD_510_17.

23.

Proteomic changes in Mycobacterium tuberculosis H37Rv under hyperglycemic conditions favour its growth through altered expression of Tgs3(Rv3234c) and supportive proteins (Rv0547c, AcrA1 and Mpa).

Kundu J, Verma A, Verma I, Bhadada SK, Sharma S.

Tuberculosis (Edinb). 2019 Mar;115:154-160. doi: 10.1016/j.tube.2019.03.006. Epub 2019 Mar 20.

PMID:
30948171
24.

BRCA1/BARD1-dependent ubiquitination of NF2 regulates Hippo-YAP1 signaling.

Verma S, Yeddula N, Soda Y, Zhu Q, Pao G, Moresco J, Diedrich JK, Hong A, Plouffe S, Moroishi T, Guan KL, Verma IM.

Proc Natl Acad Sci U S A. 2019 Apr 9;116(15):7363-7370. doi: 10.1073/pnas.1822155116. Epub 2019 Mar 27.

25.

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.

Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, Datar C, Verma IC, Puri RD, Zollino M, Bachmann-Gagescu R, Niedrist D, Papik M, Figueiro-Silva J, Masood R, Zweier M, Kraemer D, Lincoln S, Rodan L; Undiagnosed Diseases Network (UDN), Passemard S, Drunat S, Verloes A, Horn AHC, Sticht H, Steinfeld R, Plecko B, Latal B, Jenni O, Asadollahi R, Rauch A.

Genet Med. 2019 Sep;21(9):2043-2058. doi: 10.1038/s41436-019-0464-7. Epub 2019 Mar 7.

26.

Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD.

Pandita S, Ramachandran V, Balakrishnan P, Rolfs A, Brandau O, Eichler S, Bhalla AK, Khullar D, Amitabh V, Ramanarayanan S, Kher V, Verma J, Kohli S, Saxena R, Verma IC.

J Hum Genet. 2019 May;64(5):409-419. doi: 10.1038/s10038-019-0582-8. Epub 2019 Feb 28.

PMID:
30816285
27.

Expression analysis of genes associated with sucrose accumulation and its effect on source-sink relationship in high sucrose accumulating early maturing sugarcane variety.

Verma I, Roopendra K, Sharma A, Chandra A, Kamal A.

Physiol Mol Biol Plants. 2019 Jan;25(1):207-220. doi: 10.1007/s12298-018-0627-z. Epub 2018 Dec 7.

28.

Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome.

Arora V, Aggarwal S, Bijarnia S, Lall M, Joshi A, Dua-Puri R, Arora U, Verma I.

Mol Syndromol. 2019 Jan;9(6):312-318. doi: 10.1159/000494995. Epub 2018 Dec 14.

29.

The first case of antenatal presentation in COG8-congenital disorder of glycosylation with a novel splice site mutation and an extended phenotype.

Arora V, Puri RD, Bhai P, Sharma N, Bijarnia-Mahay S, Dimri N, Baijal A, Saxena R, Verma I.

Am J Med Genet A. 2019 Mar;179(3):480-485. doi: 10.1002/ajmg.a.61030. Epub 2019 Jan 28.

PMID:
30690882
30.

Autosomal Dominant Polycystic Kidney Disease: Presence of Hypomorphic Alleles in PKD1 Gene.

Pandita S, Khullar D, Saxena R, Verma IC.

Indian J Nephrol. 2018 Nov-Dec;28(6):482-484. doi: 10.4103/ijn.IJN_236_17.

31.

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India.

Verma IC, Puri R, Venkataswamy E, Tayal T, Nampoorthiri S, Andrew C, Kabra M, Bagga R, Gowda M, Batra M, Hegde S, Kaul A, Gupta N, Mishra P, Subramanian JG, Lingaiah S, Akhtar R, Kidangan F, Chandran R, Kiran C, Ravi Kumar GR, Ramprasad VL, Kadam P.

J Obstet Gynaecol India. 2018 Dec;68(6):462-470. doi: 10.1007/s13224-017-1061-9. Epub 2018 Jan 25.

32.

SNW1, a Novel Transcriptional Regulator of the NF-κB Pathway.

Verma S, De Jesus P, Chanda SK, Verma IM.

Mol Cell Biol. 2019 Jan 16;39(3). pii: e00415-18. doi: 10.1128/MCB.00415-18. Print 2019 Feb 1.

33.

Transcriptional Profile of Mycobacterium tuberculosis in an in vitro Model of Intraocular Tuberculosis.

Abhishek S, Saikia UN, Gupta A, Bansal R, Gupta V, Singh N, Laal S, Verma I.

Front Cell Infect Microbiol. 2018 Oct 2;8:330. doi: 10.3389/fcimb.2018.00330. eCollection 2018.

34.

Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.

Bijarnia-Mahay S, Häberle J, Jalan AB, Puri RD, Kohli S, Kudalkar K, Rüfenacht V, Gupta D, Maurya D, Verma J, Shigematsu Y, Yamaguchi S, Saxena R, Verma IC.

Orphanet J Rare Dis. 2018 Oct 1;13(1):174. doi: 10.1186/s13023-018-0908-1.

35.

Cleavage of the leptin receptor by matrix metalloproteinase-2 promotes leptin resistance and obesity in mice.

Mazor R, Friedmann-Morvinski D, Alsaigh T, Kleifeld O, Kistler EB, Rousso-Noori L, Huang C, Li JB, Verma IM, Schmid-Schönbein GW.

Sci Transl Med. 2018 Aug 22;10(455). pii: eaah6324. doi: 10.1126/scitranslmed.aah6324.

PMID:
30135249
36.

Directed differentiation of mouse P19 embryonal carcinoma cells to neural cells in a serum- and retinoic acid-free culture medium.

Verma I, Seshagiri PB.

In Vitro Cell Dev Biol Anim. 2018 Sep;54(8):567-579. doi: 10.1007/s11626-018-0275-1. Epub 2018 Jul 20.

PMID:
30030768
37.

Poly(l-lysine)-Coated Liquid Crystal Droplets for Sensitive Detection of DNA and Their Applications in Controlled Release of Drug Molecules.

Verma I, Sidiq S, Pal SK.

ACS Omega. 2017 Nov 30;2(11):7936-7945. doi: 10.1021/acsomega.7b01175. Epub 2017 Nov 15.

38.

Mycobacterium tuberculosis H37Rv expresses differential proteome during intracellular survival within alveolar epithelial cells compared with macrophages.

Agarwal S, Ghosh S, Sharma S, Kaur K, Verma I.

Pathog Dis. 2018 Aug 1;76(6). doi: 10.1093/femspd/fty058.

PMID:
30010849
39.

Analysis of differential expression of protease-activated receptors in patients with allergic fungal rhinosinusitis.

Sawhney S, Bansal S, Kalyan M, Verma I, Singh Virk R, Gupta AK.

Allergy Rhinol (Providence). 2018 Apr 9;9:2152656718764199. doi: 10.1177/2152656718764199. eCollection 2018 Jan-Dec.

40.

Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Shibata N, Hasegawa Y, Yamada K, Kobayashi H, Purevsuren J, Yang Y, Dung VC, Khanh NN, Verma IC, Bijarnia-Mahay S, Lee DH, Niu DM, Hoffmann GF, Shigematsu Y, Fukao T, Fukuda S, Taketani T, Yamaguchi S.

Mol Genet Metab Rep. 2018 May 21;16:5-10. doi: 10.1016/j.ymgmr.2018.05.003. eCollection 2018 Sep.

41.

Macroporous Dual-compartment Hydrogels for Minimally Invasive Transplantation of Primary Human Hepatocytes.

Seale N, Ramaswamy S, Shih YR, Verma I, Varghese S.

Transplantation. 2018 Sep;102(9):e373-e381. doi: 10.1097/TP.0000000000002330.

42.

Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases.

Singh K, Puri RD, Bhai P, Arya AD, Chawla G, Saxena R, Verma IC.

J Pediatr Endocrinol Metab. 2018 Jul 26;31(7):799-807. doi: 10.1515/jpem-2018-0023.

PMID:
29874194
43.

Heterochromatin-Encoded Satellite RNAs Induce Breast Cancer.

Zhu Q, Hoong N, Aslanian A, Hara T, Benner C, Heinz S, Miga KH, Ke E, Verma S, Soroczynski J, Yates JR 3rd, Hunter T, Verma IM.

Mol Cell. 2018 Jun 7;70(5):842-853.e7. doi: 10.1016/j.molcel.2018.04.023. Epub 2018 May 31.

44.

Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent in situ hybridization.

Eswarachari V, Kadam P, Movva S, Lingaiah S, Akther RM, Kidangan FX, Gowda KC, Golakoti RRK, Lall M, Mahajan S, Saviour P, Puri R, Verma IC, Vedam RL.

J Matern Fetal Neonatal Med. 2018 Jun 13:1-4. doi: 10.1080/14767058.2018.1481383. [Epub ahead of print]

PMID:
29793366
45.

Clinical and molecular characterization of Indian patients with fructose-1, 6-bisphosphatase deficiency: Identification of a frequent variant (E281K).

Bhai P, Bijarnia-Mahay S, Puri RD, Saxena R, Gupta D, Kotecha U, Sachdev A, Gupta D, Vyas V, Agarwal D, Jain V, Bansal RK, Kumar TG, Verma IC.

Ann Hum Genet. 2018 Sep;82(5):309-317. doi: 10.1111/ahg.12256. Epub 2018 May 18.

PMID:
29774539
46.

Estimation of cortisol levels in patients with premalignant disorders and oral squamous cell carcinoma.

Sharma P, Sandhu SV, Bhandari R, Verma I, Bhullar RK, Khangura RK.

J Oral Maxillofac Pathol. 2018 Jan-Apr;22(1):27-34. doi: 10.4103/jomfp.JOMFP_181_16.

47.

Autologous and Heterologous Cell Therapy for Hemophilia B toward Functional Restoration of Factor IX.

Ramaswamy S, Tonnu N, Menon T, Lewis BM, Green KT, Wampler D, Monahan PE, Verma IM.

Cell Rep. 2018 May 1;23(5):1565-1580. doi: 10.1016/j.celrep.2018.03.121.

48.

Glioblastoma Model Using Human Cerebral Organoids.

Ogawa J, Pao GM, Shokhirev MN, Verma IM.

Cell Rep. 2018 Apr 24;23(4):1220-1229. doi: 10.1016/j.celrep.2018.03.105.

49.

Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease.

Pandita S, Maurya D, Ramachandran V, Verma J, Kohli S, Saxena R, Verma IC.

Int J Mol Cell Med. 2017 Summer;6(3):164-173. doi: 10.22088/acadpub.BUMS.6.3.164. Epub 2017 Sep 26.

50.

Targeting CREB Pathway Suppresses Small Cell Lung Cancer.

Xia Y, Zhan C, Feng M, Leblanc M, Ke E, Yeddula N, Verma IM.

Mol Cancer Res. 2018 May;16(5):825-832. doi: 10.1158/1541-7786.MCR-17-0576. Epub 2018 Mar 9.

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