Publications by authors named "Vanita Vanita"

28Publications

Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin.

Clin Exp Ophthalmol 2020 04 3;48(3):343-355. Epub 2020 Feb 3.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, India.

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http://dx.doi.org/10.1111/ceo.13719DOI Listing
April 2020

Pre-clinical and cellular toxicity evaluation of 7-methylxanthine: an investigational drug for the treatment of myopia.

Drug Chem Toxicol 2019 Jul 12:1-10. Epub 2019 Jul 12.

a Department of Pharmaceutical Sciences , Guru Nanak Dev University , Amritsar , India.

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http://dx.doi.org/10.1080/01480545.2019.1635615DOI Listing
July 2019

Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort.

Gene 2019 Aug 25;709:25-35. Epub 2019 May 25.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2019.05.035DOI Listing
August 2019

A novel mutation in MERTK for rod-cone dystrophy in a North Indian family.

Can J Ophthalmol 2019 02 11;54(1):40-50. Epub 2018 Apr 11.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, India. Electronic address:

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http://dx.doi.org/10.1016/j.jcjo.2018.02.008DOI Listing
February 2019

Screening of Arg368His as predominant mutation in North Indian primary open angle glaucoma and juvenile onset glaucoma patients.

Mol Biol Res Commun 2018 Dec;7(4):181-186

Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, India.

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http://dx.doi.org/10.22099/mbrc.2018.30630.1344DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363938PMC
December 2018

A novel mutation in the PRPF31 in a North Indian adRP family with incomplete penetrance.

Doc Ophthalmol 2018 10 11;137(2):103-119. Epub 2018 Aug 11.

Department of Human Genetics, Guru Nanak Dev University (GNDU), Amritsar, Punjab, 143005, India.

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http://link.springer.com/10.1007/s10633-018-9654-x
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http://dx.doi.org/10.1007/s10633-018-9654-xDOI Listing
October 2018

Association of aldose reductase gene (AKR1B1) polymorphism with diabetic retinopathy.

Diabetes Res Clin Pract 2016 Nov 8;121:41-48. Epub 2016 Sep 8.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India. Electronic address:

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http://dx.doi.org/10.1016/j.diabres.2016.08.019DOI Listing
November 2016

Association analysis of PPARγ (p.Pro12Ala) polymorphism with type 2 diabetic retinopathy in patients from north India.

Ophthalmic Genet 2017 May-Jun;38(3):217-221. Epub 2016 Jul 18.

a Department of Human Genetics , Guru Nanak Dev University , Amritsar , Punjab , India.

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https://www.tandfonline.com/doi/full/10.1080/13816810.2016.1
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http://dx.doi.org/10.1080/13816810.2016.1193879DOI Listing
November 2017

Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium.

J Mater Chem B 2016 Jun 5;4(21):3750-3759. Epub 2016 May 5.

Department of Chemistry, UGC Centre for Advanced Studies, Guru Nanak Dev University, Amritsar 143 005, India.

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http://dx.doi.org/10.1039/c6tb00512hDOI Listing
June 2016

Ratiometric fluorophore for quantification of iodide under physiological conditions: applications in urine analysis and live cell imaging.

Org Biomol Chem 2016 Apr 15;14(14):3536-43. Epub 2016 Mar 15.

Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, Punjab, India.

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http://dx.doi.org/10.1039/c6ob00373gDOI Listing
April 2016

A catalytic chemodosimetric approach for detection of nanomolar cyanide ions in water, blood serum and live cell imaging.

Org Biomol Chem 2015 Dec 25;13(45):11129-39. Epub 2015 Sep 25.

Department of Chemistry, UGC Centre for Advanced Studies, Guru Nanak Dev University, Amritsar 143 005, India.

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http://dx.doi.org/10.1039/c5ob01617gDOI Listing
December 2015

Bay functionalized perylenediimide as a deaggregation based intracellular fluorescent probe for perchlorate.

Chem Commun (Camb) 2014 Nov;50(90):13994-7

Department of Chemistry, UGC Centre for Advanced Studies, Guru Nanak Dev University, Amritsar 143 005, India.

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http://dx.doi.org/10.1039/c4cc06765gDOI Listing
November 2014

Differential effect of cataract-associated mutations in MAF on transactivation of MAF target genes.

Mol Cell Biochem 2014 Nov 27;396(1-2):137-45. Epub 2014 Jul 27.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, 143005, Punjab, India,

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http://dx.doi.org/10.1007/s11010-014-2150-zDOI Listing
November 2014

Nanomolar fluorogenic detection of Al(III) by a series of Schiff bases in an aqueous system and their application in cell imaging.

Org Biomol Chem 2014 Jul;12(25):4445-53

Department of Chemistry, UGC Center for Advance Studies, Guru Nanak Dev University, Amritsar 143005, Punjab, India.

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http://dx.doi.org/10.1039/c4ob00329bDOI Listing
July 2014

Association of RAGE (p.Gly82Ser) and MnSOD (p.Val16Ala) polymorphisms with diabetic retinopathy in T2DM patients from north India.

Authors:
Vanita Vanita

Diabetes Res Clin Pract 2014 Apr 9;104(1):155-62. Epub 2014 Jan 9.

Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India. Electronic address:

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http://dx.doi.org/10.1016/j.diabres.2013.12.059DOI Listing
April 2014

A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family.

Exp Eye Res 2012 Nov 3;104:82-8. Epub 2012 Oct 3.

Department of Human Genetics, Guru Nanak Dev University, GT Road, Amritsar, Punjab, India.

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http://dx.doi.org/10.1016/j.exer.2012.09.010DOI Listing
November 2012

A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type.

Mol Cell Biochem 2012 Sep 6;368(1-2):167-72. Epub 2012 Jun 6.

Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, Punjab, India.

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http://link.springer.com/content/pdf/10.1007/s11010-012-1355
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http://link.springer.com/10.1007/s11010-012-1355-2
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http://dx.doi.org/10.1007/s11010-012-1355-2DOI Listing
September 2012

Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.

Genet Test Mol Biomarkers 2009 Feb;13(1):43-9

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://dx.doi.org/10.1089/gtmb.2008.0055DOI Listing
February 2009

Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.

Mol Vis 2009 4;15:476-81. Epub 2009 Mar 4.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650718PMC
April 2009

A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.

Mol Vis 2008 Jun 17;14:1171-5. Epub 2008 Jun 17.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435161PMC
June 2008

A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.

Mol Vis 2008 Feb 9;14:323-6. Epub 2008 Feb 9.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2255026PMC
February 2008

A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.

Mol Vis 2007 Oct 25;13:2035-40. Epub 2007 Oct 25.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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October 2007

A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.

Mol Vis 2007 Sep 11;13:1657-65. Epub 2007 Sep 11.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://www.molvis.org/molvis/v17/a151/mv-v17-a151-ding.pdf
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September 2007

A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.

Mol Vis 2007 Jun 4;13:797-803. Epub 2007 Jun 4.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768755PMC
June 2007

A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.

Mol Vis 2006 Oct 18;12:1217-22. Epub 2006 Oct 18.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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October 2006

A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.

Mol Vis 2006 May 22;12:518-22. Epub 2006 May 22.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, Punjab, India.

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May 2006

Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.

Mol Vis 2006 Feb 21;12:93-9. Epub 2006 Feb 21.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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February 2006

A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.

Am J Med Genet A 2006 Mar;140(6):558-66

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.

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http://dx.doi.org/10.1002/ajmg.a.31126DOI Listing
March 2006