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HTS driven by fluorescence lifetime detection of FRET identifies activators and inhibitors of cardiac myosin

SLAS discovery, 2023-07, Vol.28 (5), p.223-232

2023

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Ocular Tolerability and Efficacy of Ebastine Colloidal Formulation in Allergic Conjunctivitis

International journal of pharmaceutical sciences and drug research, 2019-07, p.129-136

2019

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TREATMENT OF CONSTITUTIONAL PRECOCIOUS PUBERTY WITH MEDROXYPROGESTERONE ACETATE

Proceedings of the Royal Society of Medicine, 1965-02, Vol.58, p.123

SURTI, N R

1965

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Placental Transfusion as an Intrauterine Phenomenon in Deliveries Complicated by Foetal Distress

BMJ, 1969-04, Vol.2 (5648), p.11-13

1969

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Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis

Haematologica (Roma), 2011-08, Vol.96 (8), p.1144-1152

2011

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Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads

Annals of human genetics, 2020-03, Vol.84 (2), p.125-140

2020

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Biodegradable in situ Gel for Subcutaneous Administration of Simvastatin for Osteoporosis

Indian journal of pharmaceutical sciences, 2018-03, Vol.80 (2)

2018

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Reproductive outcomes in individuals with chromosomal reciprocal translocations

Genetics in medicine, 2021-09, Vol.23 (9), p.1753-1760

2021

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Rapid Response to Syphilis Outbreak among Female Sex Workers

Indian journal of community medicine, 2017-10, Vol.42 (4), p.214-217

2017

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High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Clinical genetics, 2016-01, Vol.89 (1), p.82-87

2016

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Abstract MP215: Endothelial Colony Forming Cell Derived Exosomes Promote Angiogenesis And Cardiac Repair Post Myocardial Infarction

Circulation research, 2021-09, Vol.129 (Suppl_1)

2021

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Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

Nature genetics, 2009-03, Vol.41 (3), p.348-353

2009

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A new alternative for a transjugular intrahepatic portosystemic shunt: EUS-guided creation of an intrahepatic portosystemic shunt (with video)

Gastrointestinal endoscopy, 2009-04, Vol.69 (4), p.941-947

2009

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Application of chromosomal microarray in the evaluation of abnormal prenatal findings

Clinical genetics, 2013-07, Vol.84 (1), p.47-54

2013

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Common variants at 30 loci contribute to polygenic dyslipidemia

Nature genetics, 2009-01, Vol.41 (1), p.56-65

2009

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NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

Journal of medical genetics, 2011-08, Vol.48 (8), p.540-548

2011

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Nature genetics, 2010-03, Vol.42 (3), p.203-209

2010

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P–553 Women with molar pregnancies have a genetic susceptibility to aneuploid miscarriages

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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Copy number alterations involving 59 ACMG‐recommended secondary findings genes

Clinical genetics, 2020-12, Vol.98 (6), p.577-588

2020

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Identification by Mass Spectrometry and Functional Characterization of Two Phosphorylation Sites of KCNQ2/KCNQ3 Channels

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (49), p.17828-17833

2005

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Air and fluid leak tests after NOTES procedures: a pilot study in a live porcine model (with videos)

Gastrointestinal endoscopy, 2008-09, Vol.68 (3), p.513-519

2008

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Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3

American journal of medical genetics. Part A, 2017-12, Vol.173 (12), p.3153-3157

2017

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Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features

Human mutation, 2012-04, Vol.33 (4), p.728-740

2012

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HTS driven by fluorescence lifetime detection of FRET identifies activators and inhibitors of cardiac myosin

Ocular Tolerability and Efficacy of Ebastine Colloidal Formulation in Allergic Conjunctivitis

TREATMENT OF CONSTITUTIONAL PRECOCIOUS PUBERTY WITH MEDROXYPROGESTERONE ACETATE

Placental Transfusion as an Intrauterine Phenomenon in Deliveries Complicated by Foetal Distress

Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis

Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads

Biodegradable in situ Gel for Subcutaneous Administration of Simvastatin for Osteoporosis

Reproductive outcomes in individuals with chromosomal reciprocal translocations

Rapid Response to Syphilis Outbreak among Female Sex Workers

High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Abstract MP215: Endothelial Colony Forming Cell Derived Exosomes Promote Angiogenesis And Cardiac Repair Post Myocardial Infarction

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

A new alternative for a transjugular intrahepatic portosystemic shunt: EUS-guided creation of an intrahepatic portosystemic shunt (with video)

Application of chromosomal microarray in the evaluation of abnormal prenatal findings

Common variants at 30 loci contribute to polygenic dyslipidemia

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

P–553 Women with molar pregnancies have a genetic susceptibility to aneuploid miscarriages

Discovery, Structure–Activity Relationships, and In Vivo Evaluation of Novel Aryl Amides as Brain Penetrant Adaptor Protein 2‑Associated Kinase 1 (AAK1) Inhibitors for the Treatment of Neuropathic Pain

Copy number alterations involving 59 ACMG‐recommended secondary findings genes

Identification by Mass Spectrometry and Functional Characterization of Two Phosphorylation Sites of KCNQ2/KCNQ3 Channels

Air and fluid leak tests after NOTES procedures: a pilot study in a live porcine model (with videos)

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3

Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features

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