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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

PLoS genetics, 2009-09, Vol.5 (9), p.e1000649

2009

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Technology Innovation in Manufacturing

First edition., 2023

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Germline Pathogenic Variants in the Ataxia Telangiectasia Mutated ( ATM ) Gene are Associated with High and Moderate Risks for Multiple Cancers

Cancer prevention research (Philadelphia, Pa.), 2021-04, Vol.14 (4), p.433-440

2021

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dbEM: A database of epigenetic modifiers curated from cancerous and normal genomes

Scientific reports, 2016-01, Vol.6 (1), p.19340-19340, Article 19340

2016

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Translational initiation factor eIF5 replaces eIF1 on the 40S ribosomal subunit to promote start-codon recognition

eLife, 2018-11, Vol.7

2018

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A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction

PLoS genetics, 2008-07, Vol.4 (7), p.e1000125-e1000125

2008

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Fine-needle aspiration cytology: a reliable tool in the diagnosis of salivary gland lesions

Journal of oral pathology & medicine, 2012-01, Vol.41 (1), p.106-112

2012

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Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

The Journal of physiology, 2008-07, Vol.586 (14), p.3405-3423

2008

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Breeding ecology of the Asian openbill in eastern Nepal: Larger trees support higher fledgling success

Ecology and evolution, 2024-06, Vol.14 (6), p.e11504-n/a

2024

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Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8

Scientific reports, 2016-05, Vol.6 (1), p.26278-26278, Article 26278

2016

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A prospective case-control study of disability, quality of life, and functional impairment of shoulder movements after latissimus dorsi myocutaneous flap reconstruction in breast cancer patients

Turkish journal of surgery, 2024-03, Vol.40 (1), p.65-72

2024

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The Himalayas as a Directional Barrier to Gene Flow

American journal of human genetics, 2007-05, Vol.80 (5), p.884-894

2007

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KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

Brain (London, England : 1878), 2003-12, Vol.126 (12), p.2726-2737

2003

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Nature genetics, 1998-01, Vol.18 (1), p.53-55

1998

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Identification of pathogenic retrotransposon insertions in cancer predisposition genes

Cancer genetics, 2017-10, Vol.216-217, p.159-169

2017

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Role of Oral Enzymes in Post Operative Septoplasty Cases

Indian journal of otolaryngology, and head, and neck surgery, 2019-11, Vol.71 (Suppl 3), p.1663-1667

2019

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Role of buffalo in the socioeconomic development of rural Asia: Current status and future prospectus

Animal science journal, 2003-12, Vol.74 (6), p.443-455

2003

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Increased expression of CK8 and CK18 in leukoplakia, oral submucous fibrosis, and oral squamous cell carcinoma: An immunohistochemistry study

Oral surgery, oral medicine, oral pathology and oral radiology, 2012-02, Vol.113 (2), p.245-253

2012

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Correlation between dental caries experience and mutans streptococci counts using saliva and plaque as microbial risk indicators in 3-8 year old children. A cross Sectional study

Journal of clinical and experimental dentistry, 2015, p.e114-e118

2015

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ROLE OF NEWER MEDICAL EDUCATION TECHNOLOGIES AND ATTITUDE AND COMMUNICATION (AT-COM) MODULE IN TEACHING OTORHINOLARYNGOLOGY

Journal of evolution of medical and dental sciences, 2017-11, Vol.6 (90), p.6301-6303

Singh Nanda, Manpreet

2017

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The Macrophage Cell Surface Glyceraldehyde-3-phosphate Dehydrogenase Is a Novel Transferrin Receptor

The Journal of biological chemistry, 2007-02, Vol.282 (5), p.3252-3261

2007

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An RNAi-independent role of AP1-like stress response factor Pap1 in centromere and mating-type silencing in Schizosaccaromyces pombe

Journal of biosciences, 2021-09, Vol.46 (3), Article 74

2021

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Treating mucormycosis using a multimodality approach: a case series

Journal of wound care, 2018-11, Vol.27 (11), p.735-742

2018

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Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

Epilepsia (Copenhagen), 2009-07, Vol.50 (7), p.1752-1759

2009

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A novel potassium channel gene, KCNQ2 , is mutated in an inherited epilepsy of newborns

Nature genetics, 1998-01, Vol.18 (1), p.25-29

1998

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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

Technology Innovation in Manufacturing

Germline Pathogenic Variants in the Ataxia Telangiectasia Mutated ( ATM ) Gene are Associated with High and Moderate Risks for Multiple Cancers

dbEM: A database of epigenetic modifiers curated from cancerous and normal genomes

Translational initiation factor eIF5 replaces eIF1 on the 40S ribosomal subunit to promote start-codon recognition

A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction

Fine-needle aspiration cytology: a reliable tool in the diagnosis of salivary gland lesions

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

Breeding ecology of the Asian openbill in eastern Nepal: Larger trees support higher fledgling success

Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8

A prospective case-control study of disability, quality of life, and functional impairment of shoulder movements after latissimus dorsi myocutaneous flap reconstruction in breast cancer patients

The Himalayas as a Directional Barrier to Gene Flow

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Identification of pathogenic retrotransposon insertions in cancer predisposition genes

Role of Oral Enzymes in Post Operative Septoplasty Cases

Role of buffalo in the socioeconomic development of rural Asia: Current status and future prospectus

Increased expression of CK8 and CK18 in leukoplakia, oral submucous fibrosis, and oral squamous cell carcinoma: An immunohistochemistry study

Correlation between dental caries experience and mutans streptococci counts using saliva and plaque as microbial risk indicators in 3-8 year old children. A cross Sectional study

ROLE OF NEWER MEDICAL EDUCATION TECHNOLOGIES AND ATTITUDE AND COMMUNICATION (AT-COM) MODULE IN TEACHING OTORHINOLARYNGOLOGY

The Macrophage Cell Surface Glyceraldehyde-3-phosphate Dehydrogenase Is a Novel Transferrin Receptor

An RNAi-independent role of AP1-like stress response factor Pap1 in centromere and mating-type silencing in Schizosaccaromyces pombe

Treating mucormycosis using a multimodality approach: a case series

Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

A novel potassium channel gene, KCNQ2 , is mutated in an inherited epilepsy of newborns

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