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The Drosophila drop-dead gene is required for eggshell integrity

PloS one, 2023-12, Vol.18 (12), p.e0295412-e0295412

2023

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Spinal teratoma with salivary glandular differentiation

Neurology India, 2009-11, Vol.57 (6), p.821

2009

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Ovariectomy Via 12/15-lipoxygenase Augments Angiotensin II-Induced Hypertension and Its Pathogenesis in Female Mice

Hypertension (Dallas, Tex. 1979), 2023-06, Vol.80 (6), p.1245-1257

2023

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Maternal and fetal outcomes in pregnant women with acute hepatitis E virus infection

Annals of internal medicine, 2007-07, Vol.147 (1), p.28

2007

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Association of functional genetic variants of CTLA4 with reduced serum CTLA4 protein levels and increased risk to idiopathic recurrent miscarriages

Fertility and sterility, 2016-10, Vol.106 (5), p.1115-1123.e6

2016

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Autosomal recessive spinocerebellar ataxia‐20 due to a novel SNX14 variant in an Indian girl

American journal of medical genetics. Part A, 2022-06, Vol.188 (6), p.1909-1914

2022

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UK guidelines on the management of iron deficiency in pregnancy

British journal of haematology, 2012-03, Vol.156 (5), p.588-600

2012

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Pearson Syndrome: Spontaneously Recovering Anemia and Hypoparathyroidism

Indian journal of pediatrics, 2020-12, Vol.87 (12), p.1070-1072

2020

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Spectrum of prenatally detected central nervous system malformations: Neural tube defects continue to be the leading foetal malformation

Indian journal of medical research (New Delhi, India : 1994), 2017-04, Vol.145 (4), p.471

2017

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Central CYP1B1 (Cytochrome P450 1B1)-Estradiol Metabolite 2-Methoxyestradiol Protects From Hypertension and Neuroinflammation in Female Mice

Hypertension (Dallas, Tex. 1979), 2020-04, Vol.75 (4), p.1054-1062

2020

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Hyperekplexia: A forgotten diagnosis clinched by next-generation sequencing

Neurology India, 2017-09, Vol.65 (5), p.1065

2017

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Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

American journal of human genetics, 2019-03, Vol.104 (3), p.439-453

2019

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2-Methoxyestradiol Ameliorates Angiotensin II-Induced Hypertension by Inhibiting Cytosolic Phospholipase A 2 α Activity in Female Mice

Hypertension (Dallas, Tex. 1979), 2021-11, Vol.78 (5), p.1368-1381

2021

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An Alba-domain protein required for proteome remodelling during trypanosome differentiation and host transition

PLoS pathogens, 2021-01, Vol.17 (1), p.e1009239-e1009239

2021

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De novo SOX11 mutations cause Coffin-Siris syndrome

Nature communications, 2014-06, Vol.5 (1), p.4011-4011, Article 4011

2014

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Clinical and Mutation Spectra of Cockayne Syndrome in India

Neurology India, 2021-03, Vol.69 (2), p.362-366

2021

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How we manage the haematological aspects of major obstetric haemorrhage

British journal of haematology, 2014-01, Vol.164 (2), p.177-188

2014

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Cell salvage and donor blood transfusion during cesarean section: A pragmatic, multicentre randomised controlled trial (SALVO)

PLoS medicine, 2017-12, Vol.14 (12), p.e1002471-e1002471

2017

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Association of Anthropometric Indices with Menstrual Abnormality among Nursing Students of Nepal: A Cross-Sectional Study

Journal of obesity, 2022-03, Vol.2022, p.6755436-8

2022

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Double segment chromosomal imbalance due to inherited chromosomal translocation: Detection by cytogenetic microarray

Indian pediatrics, 2017-10, Vol.54 (10), p.879-881

2017

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Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders

American journal of medical genetics. Part A, 2016-06, Vol.170A (6), p.1622-1625

2016

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Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer

European journal of pharmaceutics and biopharmaceutics, 2017-05, Vol.114, p.108-118

2017

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An Unusual Case of Rectal Bleed in an Adolescent: Solitary Rectal Ulcer Syndrome Mimicking Rectosigmoid Malignancy

Journal of clinical and diagnostic research, 2022-02, Vol.16 (2), p.OD04-OD06

2022

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A randomised controlled trial and economic evaluation of intraoperative cell salvage during caesarean section in women at risk of haemorrhage: the SALVO (cell SALVage in Obstetrics) trial

Health technology assessment (Winchester, England), 2018-01, Vol.22 (2), p.1-88

2018

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Platelet-specific collagen receptor glycoprotein VI gene variants affect recurrent pregnancy loss

Fertility and sterility, 2014-10, Vol.102 (4), p.1078-1084.e3

2014

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The Drosophila drop-dead gene is required for eggshell integrity

Spinal teratoma with salivary glandular differentiation

Ovariectomy Via 12/15-lipoxygenase Augments Angiotensin II-Induced Hypertension and Its Pathogenesis in Female Mice

Maternal and fetal outcomes in pregnant women with acute hepatitis E virus infection

Association of functional genetic variants of CTLA4 with reduced serum CTLA4 protein levels and increased risk to idiopathic recurrent miscarriages

Autosomal recessive spinocerebellar ataxia‐20 due to a novel SNX14 variant in an Indian girl

UK guidelines on the management of iron deficiency in pregnancy

Pearson Syndrome: Spontaneously Recovering Anemia and Hypoparathyroidism

Spectrum of prenatally detected central nervous system malformations: Neural tube defects continue to be the leading foetal malformation

Central CYP1B1 (Cytochrome P450 1B1)-Estradiol Metabolite 2-Methoxyestradiol Protects From Hypertension and Neuroinflammation in Female Mice

Hyperekplexia: A forgotten diagnosis clinched by next-generation sequencing

Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

2-Methoxyestradiol Ameliorates Angiotensin II-Induced Hypertension by Inhibiting Cytosolic Phospholipase A 2 α Activity in Female Mice

An Alba-domain protein required for proteome remodelling during trypanosome differentiation and host transition

De novo SOX11 mutations cause Coffin-Siris syndrome

Clinical and Mutation Spectra of Cockayne Syndrome in India

How we manage the haematological aspects of major obstetric haemorrhage

Cell salvage and donor blood transfusion during cesarean section: A pragmatic, multicentre randomised controlled trial (SALVO)

Association of Anthropometric Indices with Menstrual Abnormality among Nursing Students of Nepal: A Cross-Sectional Study

Double segment chromosomal imbalance due to inherited chromosomal translocation: Detection by cytogenetic microarray

Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders

Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer

An Unusual Case of Rectal Bleed in an Adolescent: Solitary Rectal Ulcer Syndrome Mimicking Rectosigmoid Malignancy

A randomised controlled trial and economic evaluation of intraoperative cell salvage during caesarean section in women at risk of haemorrhage: the SALVO (cell SALVage in Obstetrics) trial

Platelet-specific collagen receptor glycoprotein VI gene variants affect recurrent pregnancy loss

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