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A Dysmorphic Child with a Pericentric Inversion of Chromosome 8

Case reports in pediatrics, 2012-01, Vol.2012 (2012), p.1-3

2012

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Thin‐layer mathematical modeling for drying of turmeric slices in infrared dryer

Journal of food process engineering, 2024-04, Vol.47 (4), p.n/a

2024

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COVID-19 and its impact on neurological manifestations and mental health: the present scenario

Neurological sciences, 2020-11, Vol.41 (11), p.3015-3020

2020

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Performance of light weight concrete with different aggregates—a comprehensive review

Discover Civil Engineering, 2024-08, Vol.1 (1), Article 46

2024

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Membrane-bound O-acyltransferase 7 (MBOAT7)-driven phosphatidylinositol remodeling in advanced liver disease

Journal of lipid research, 2022-07, Vol.63 (7), p.100234, Article 100234

2022

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Identification of key functional pathways: arginine biosynthesis and IL-17 signalling in placental decidua of unexplained recurrent pregnancy loss through RNA sequencing-a case series

Middle East Fertility Society journal, 2024-12, Vol.29 (1), p.31

2024

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Imine stilbene analog ameliorate isoproterenol-induced cardiac hypertrophy and hydrogen peroxide-induced apoptosis

Free radical biology & medicine, 2020-06, Vol.153, p.80-88

2020

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Oleosin Is Bifunctional Enzyme That Has Both Monoacylglycerol Acyltransferase and Phospholipase Activities

The Journal of biological chemistry, 2012-01, Vol.287 (3), p.1946-1954

2012

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A Rare Case of Dysmorphism with Duplication in Chromosome 22

Indian journal of clinical biochemistry, 2022-10, Vol.37 (4), p.504-506

2022

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Serine/Threonine/Tyrosine Protein Kinase Phosphorylates Oleosin, a Regulator of Lipid Metabolic Functions

Plant physiology (Bethesda), 2012-05, Vol.159 (1), p.95-104

2012

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Association of genetic polymorphism of vascular endothelial growth factor in the etiology of recurrent pregnancy loss: a triad study

Journal of assisted reproduction and genetics, 2019-05, Vol.36 (5), p.979-988

2019

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MBOAT7-driven lysophosphatidylinositol acylation in adipocytes contributes to systemic glucose homeostasis

Journal of lipid research, 2023-04, Vol.64 (4), p.100349-100349, Article 100349

2023

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Are Altered Expression of Vascular Endothelial Growth Factor and Placental Growth Factor Associated with Placental Angiogenesis in Recurrent Pregnancy Loss?

Indian journal of clinical biochemistry, 2024-07, Vol.39 (3), p.387-391

2024

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Molecular Modelling and Molecular Dynamics studies of GD1A, GD1B and their complexes with BoNT/B – Perspectives in interaction and specificity

Journal of structural biology, 2012-12, Vol.180 (3), p.497-508

2012

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Epidermolysis bullosa: A report of three cases with novel heterozygous deletions in PLEC and homozygous non sense mutations in COL7A1 genes

Indian journal of dermatology, 2022-01, Vol.67 (1), p.45-49

2022

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MMD collaborates with ACSL4 and MBOAT7 to promote polyunsaturated phosphatidylinositol remodeling and susceptibility to ferroptosis

Cell reports (Cambridge), 2023-09, Vol.42 (9), p.113023-113023, Article 113023

2023

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Electrocoagulation coupled with adsorption for effective removal of eosin yellow and nigrosin dyes in aqueous solution

Journal of applied and natural science, 2019, Vol.11 (1), p.97-106

2019

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A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome 2

Faṣlnāmah-i pizishkī-i bārvar va nābārvar, 2022-04, Vol.23 (2), p.135

2022

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Leaf lipidome and transcriptome profiling of Portulaca oleracea: characterization of lysophosphatidylcholine acyltransferase

Planta, 2018-08, Vol.248 (2), p.347-367

2018

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Association of estrogen and progesterone receptor gene polymorphisms and their respective hormones in uterine leiomyomas

Tumor biology, 2016-06, Vol.37 (6), p.8067-8074

2016

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Inherited Robertsonian translocation (13;14) in a child with Down Syndrome

Journal of Biochemical and Clinical Genetics, 2020-12, Vol.3 (2), p.113-117

2020

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Haplotype analysis of IL-10 gene polymorphism in couples with spontaneous abortions and aborted fetuses

Immunologic research, 2017-08, Vol.65 (4), p.853-861

2017

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Interleukin 10 gene promoter polymorphisms in women with early‐onset pre‐eclampsia

Clinical and experimental immunology, 2014-11, Vol.178 (2), p.334-341

2014

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Role of IL-6 −174(G/C) promoter polymorphism in the etiology of early-onset preeclampsia

Inflammation research, 2015-06, Vol.64 (6), p.433-439

2015

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A Dysmorphic Child with a Pericentric Inversion of Chromosome 8

Thin‐layer mathematical modeling for drying of turmeric slices in infrared dryer

COVID-19 and its impact on neurological manifestations and mental health: the present scenario

Performance of light weight concrete with different aggregates—a comprehensive review

Membrane-bound O-acyltransferase 7 (MBOAT7)-driven phosphatidylinositol remodeling in advanced liver disease

Identification of key functional pathways: arginine biosynthesis and IL-17 signalling in placental decidua of unexplained recurrent pregnancy loss through RNA sequencing-a case series

Imine stilbene analog ameliorate isoproterenol-induced cardiac hypertrophy and hydrogen peroxide-induced apoptosis

Membrane-bound O -acyltransferase 7 (MBOAT7) shapes lysosomal lipid homeostasis and function to control alcohol-associated liver injury

Oleosin Is Bifunctional Enzyme That Has Both Monoacylglycerol Acyltransferase and Phospholipase Activities

A Rare Case of Dysmorphism with Duplication in Chromosome 22

Serine/Threonine/Tyrosine Protein Kinase Phosphorylates Oleosin, a Regulator of Lipid Metabolic Functions

Association of genetic polymorphism of vascular endothelial growth factor in the etiology of recurrent pregnancy loss: a triad study

MBOAT7-driven lysophosphatidylinositol acylation in adipocytes contributes to systemic glucose homeostasis

Are Altered Expression of Vascular Endothelial Growth Factor and Placental Growth Factor Associated with Placental Angiogenesis in Recurrent Pregnancy Loss?

Molecular Modelling and Molecular Dynamics studies of GD1A, GD1B and their complexes with BoNT/B – Perspectives in interaction and specificity

Epidermolysis bullosa: A report of three cases with novel heterozygous deletions in PLEC and homozygous non sense mutations in COL7A1 genes

MMD collaborates with ACSL4 and MBOAT7 to promote polyunsaturated phosphatidylinositol remodeling and susceptibility to ferroptosis

Electrocoagulation coupled with adsorption for effective removal of eosin yellow and nigrosin dyes in aqueous solution

A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome 2

Leaf lipidome and transcriptome profiling of Portulaca oleracea: characterization of lysophosphatidylcholine acyltransferase

Association of estrogen and progesterone receptor gene polymorphisms and their respective hormones in uterine leiomyomas

Inherited Robertsonian translocation (13;14) in a child with Down Syndrome

Haplotype analysis of IL-10 gene polymorphism in couples with spontaneous abortions and aborted fetuses

Interleukin 10 gene promoter polymorphisms in women with early‐onset pre‐eclampsia

Role of IL-6 −174(G/C) promoter polymorphism in the etiology of early-onset preeclampsia

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