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Hepatic oxylipin profiles in mouse models of Wilson disease: New insights into early hepatic manifestations

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2024-03, Vol.1869 (2), p.159446-159446, Article 159446

2024

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Assessment and Prediction of Urban Expansion Using CA-Based SLEUTH Urban Growth Model: A Case Study of Kolkata Metropolitan Area (KMA), West Bengal, India

Journal of the Indian Society of Remote Sensing, 2022-12, Vol.50 (12), p.2277-2302

2022

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Life History Responses and Gene Expression Profiles of the Nematode Pristionchus pacificus Cultured on Cryptococcus Yeasts

PloS one, 2016-10, Vol.11 (10), p.e0164881-e0164881

2016

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Urban Growth Simulations in a Medium-Sized City of Mangaluru, India, Through CA-Based SLEUTH Urban Growth Model

Journal of the Indian Society of Remote Sensing, 2023-03, Vol.51 (3), p.497-517

2023

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Identification of the periplasmic DNA receptor for natural transformation of Helicobacter pylori

Nature communications, 2019-11, Vol.10 (1), p.5357-11, Article 5357

2019

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Imaging Findings on Head Computed Tomography Scans in Victims of Intimate Partner Violence

Journal of computer assisted tomography, 2023-03, Vol.47 (2), p.307

2023

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Malignant peritoneal mesothelioma: correlation between CT imaging features and histologic subtypes

Abdominal radiology (New York), 2021-11, Vol.46 (11), p.5105-5113

2021

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Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice

PLoS genetics, 2022-03, Vol.18 (3), p.e1010114-e1010114

2022

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An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia

European journal of human genetics : EJHG, 2019-04, Vol.27 (4), p.657-662

2019

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Enhancement of weld strength of laser-welded joints of AA6061-T6 and TZM alloys via novel dual-laser warm laser shock peening

International journal of advanced manufacturing technology, 2019-09, Vol.104 (1-4), p.907-919

2019

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Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis

Brain (London, England : 1878), 2013-12, Vol.136 (Pt 12), p.3618-3624

2013

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Multidisciplinary uniform reporting for abdominal wall hernias: The key to a successful outcome

Journal of minimal access surgery, 2023-10, Vol.19 (4), p.559-560

2023

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Exceptional Tumor Regression in Diffuse Intrinsic Pontine Glioma Post-Radiotherapy: A Case Study

The American journal of case reports, 2024-09, Vol.25, p.e944869

2024

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Imaging Biomarkers of Hypothyroidism on Lung Cancer Screening CT

Current problems in diagnostic radiology, 2021-11, Vol.50 (6), p.807-810

2021

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Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

BMC medical genetics, 2019-12, Vol.20 (1), p.199-199, Article 199

2019

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Large language models in physical therapy: time to adapt and adept

Frontiers in public health, 2024-05, Vol.12, p.1364660

2024

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Dysregulated Choline, Methionine, and Aromatic Amino Acid Metabolism in Patients with Wilson Disease: Exploratory Metabolomic Profiling and Implications for Hepatic and Neurologic Phenotypes

International journal of molecular sciences, 2019-11, Vol.20 (23), p.5937

2019

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Hypomorphic PCNA mutation underlies a human DNA repair disorder

The Journal of clinical investigation, 2014-07, Vol.124 (7), p.3137-3146

2014

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Comparison of electric field modeling pipelines for transcranial direct current stimulation

Neurophysiologie clinique, 2021-08, Vol.51 (4), p.303-318

2021

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A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis

Brain (London, England : 1878), 2017-03, Vol.140 (3), p.547-554

2017

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Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genes

The journal of gene medicine, 2023-10, Vol.25 (10), p.e3513-e3513

2023

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COVID Lessons Continue: Postvaccination Somatostatin Receptor-Positive Axillary Nodes on DOTATATE Imaging

Clinical nuclear medicine, 2022-01, Vol.47 (1), p.e56-e58

2022

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Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families

Congenital anomalies, 2020-09, Vol.60 (5), p.149-150

2020

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MNS1 variant associated with situs inversus and male infertility

European journal of human genetics : EJHG, 2020-01, Vol.28 (1), p.50-55

2020

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Role of Multidetector Computed Tomography Urography in the Evaluation of Obstructive Uropathy: A Review

Curēus (Palo Alto, CA), 2023-10

2023

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Hepatic oxylipin profiles in mouse models of Wilson disease: New insights into early hepatic manifestations

Assessment and Prediction of Urban Expansion Using CA-Based SLEUTH Urban Growth Model: A Case Study of Kolkata Metropolitan Area (KMA), West Bengal, India

Life History Responses and Gene Expression Profiles of the Nematode Pristionchus pacificus Cultured on Cryptococcus Yeasts

Urban Growth Simulations in a Medium-Sized City of Mangaluru, India, Through CA-Based SLEUTH Urban Growth Model

Identification of the periplasmic DNA receptor for natural transformation of Helicobacter pylori

Imaging Findings on Head Computed Tomography Scans in Victims of Intimate Partner Violence

Malignant peritoneal mesothelioma: correlation between CT imaging features and histologic subtypes

Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice

An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia

Enhancement of weld strength of laser-welded joints of AA6061-T6 and TZM alloys via novel dual-laser warm laser shock peening

Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis

Multidisciplinary uniform reporting for abdominal wall hernias: The key to a successful outcome

Exceptional Tumor Regression in Diffuse Intrinsic Pontine Glioma Post-Radiotherapy: A Case Study

Imaging Biomarkers of Hypothyroidism on Lung Cancer Screening CT

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

Large language models in physical therapy: time to adapt and adept

Dysregulated Choline, Methionine, and Aromatic Amino Acid Metabolism in Patients with Wilson Disease: Exploratory Metabolomic Profiling and Implications for Hepatic and Neurologic Phenotypes

Hypomorphic PCNA mutation underlies a human DNA repair disorder

Comparison of electric field modeling pipelines for transcranial direct current stimulation

A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis

Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genes

COVID Lessons Continue: Postvaccination Somatostatin Receptor-Positive Axillary Nodes on DOTATATE Imaging

Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families

MNS1 variant associated with situs inversus and male infertility

Role of Multidetector Computed Tomography Urography in the Evaluation of Obstructive Uropathy: A Review

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