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Association of IL-17F rs2397084 (E126G), rs11465553 (V155I) and rs763780 (H161R) variants with rheumatoid arthritis and their effects on the stability of protein

PloS one, 2023-09, Vol.18 (9), p.e0285874-e0285874

2023

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Phylogenetic analysis of promoter regions of human Dolichol kinase (DOLK) and orthologous genes using bioinformatics tools

Open life sciences, 2023-05, Vol.18 (1), p.20220591-20220591

2023

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Exploring the Associations and Molecular Impacts of miR-146a/rs2910164 and miR-196a2/rs185070757 with Rheumatoid Arthritis in a Pakistani Population

Lifestyle genomics, 2023-01, Vol.16 (1), p.139-150

2023

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Association of IL-17F rs2397084 variants with rheumatoid arthritis and their effects on the stability of protein

PloS one, 2023-09, Vol.18 (9), p.e0285874

2023

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Association of IL-17F rs2397084

PloS one, 2023-09, Vol.18 (9), p.e0285874

2023

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Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a Pakistani Cohort

Genetics Research, 2021, Vol.2021, p.5544198-5

2021

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Association of IL-17F rs2397084 (E126G), rs11465553 (V155I) and rs763780 (H161R) variants with rheumatoid arthritis and their effects on the stability of protein

PloS one, 2023-01, Vol.18 (9)

2023

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Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic Dysfunction

Genes, 2021-11, Vol.12 (12), p.1915

2021

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Sero-prevalence of Brucellosis in Cattle and Related Human Population in District Malakand, Khyber Pakhtunkhwa, Pakistan

Acta microbiologica bulgarica, 2023-09, Vol.39 (3), p.324-329

2023

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Screening for Deleterious non-synonymous SNPs in Human CCL21 Gene using in-silico analysis

NUST Journal of Natural Sciences, 2022-02, Vol.6 (2)

2022

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A Mutation in the Thyroid Hormone Receptor Alpha Gene

The New England journal of medicine, 2012-01, Vol.366 (3), p.243-249

2012

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Treatment-Resistant Mood Disorders

Pakistan journal of medical sciences, 2024-10, Vol.40 (9), p.2141-2148

2024

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Genetic Characterization of SURMOUNT-1 Trial to Understand Tirzepatide-driven Weight Reduction

Obesity (Silver Spring, Md.), 2023-11, Vol.31, p.28-28

2023

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Solubilization of direct black 2 in mixed micellar media: insights from spectroscopic and conductometric measurements

Journal of dispersion science and technology, 2023-05, Vol.44 (6), p.1044-1053

2023

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Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis

The Journal of clinical investigation, 2016-03, Vol.126 (3), p.992-996

2016

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Open Dataset for Predicting Pilgrim Activities for Crowd Management During Hajj Using Wearable Sensors

IEEE access, 2024-01, Vol.12, p.1-1

2024

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Impact of COVID Pandemic and Hybrid teaching on Final year MBBS students' End of clerkship Exam performance

Pakistan journal of medical sciences, 2022-02, Vol.38 (1), p.113-117

2022

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Neonatal Outcomes of Very Low Birth Weight and Very Preterm Neonates: An International Comparison

The Journal of pediatrics, 2016-10, Vol.177, p.144-152.e6

2016

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Moving up without moving forward! Managing career plateau in COVID-19: a dual serial mediations

Management research review, 2022-03, Vol.45 (4), p.470-485

2022

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Performance of Ni-Sr/MgO-ZrO2 catalyst for CO2 reforming of methane: Effect of Sr addition

AIP Conference Proceedings, 2022, Vol.2610 (1)

2022

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Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia

The Journal of clinical investigation, 2010-04, Vol.120 (4), p.1345-1354

2010

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A case report of congenital insensitivity to pain and anhidrosis

Journal of Pakistan Association of Dermatologists : JPAD, 2014-09, Vol.24 (3)

2014

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A novel, missense, mutation (P81R) in the TRH receptor gene in congenital central hypothyroidism

Endocrine Abstracts, 2015-11

2015

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A novel, missense, mutation (P81R) in the TRH receptor gene in congenital central hypothyroidism

Endocrine Abstracts, 2015-10

2015

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Association of IL-17F rs2397084 (E126G), rs11465553 (V155I) and rs763780 (H161R) variants with rheumatoid arthritis and their effects on the stability of protein

Phylogenetic analysis of promoter regions of human Dolichol kinase (DOLK) and orthologous genes using bioinformatics tools

Exploring the Associations and Molecular Impacts of miR-146a/rs2910164 and miR-196a2/rs185070757 with Rheumatoid Arthritis in a Pakistani Population

Association of IL-17F rs2397084 variants with rheumatoid arthritis and their effects on the stability of protein

Association of IL-17F rs2397084

Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a Pakistani Cohort

Association of IL-17F rs2397084 (E126G), rs11465553 (V155I) and rs763780 (H161R) variants with rheumatoid arthritis and their effects on the stability of protein

Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic Dysfunction

Sero-prevalence of Brucellosis in Cattle and Related Human Population in District Malakand, Khyber Pakhtunkhwa, Pakistan

Screening for Deleterious non-synonymous SNPs in Human CCL21 Gene using in-silico analysis

A Mutation in the Thyroid Hormone Receptor Alpha Gene

Treatment-Resistant Mood Disorders

Genetic Characterization of SURMOUNT-1 Trial to Understand Tirzepatide-driven Weight Reduction

Solubilization of direct black 2 in mixed micellar media: insights from spectroscopic and conductometric measurements

Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis

Open Dataset for Predicting Pilgrim Activities for Crowd Management During Hajj Using Wearable Sensors

Impact of COVID Pandemic and Hybrid teaching on Final year MBBS students' End of clerkship Exam performance

Neonatal Outcomes of Very Low Birth Weight and Very Preterm Neonates: An International Comparison

Moving up without moving forward! Managing career plateau in COVID-19: a dual serial mediations

Performance of Ni-Sr/MgO-ZrO2 catalyst for CO2 reforming of methane: Effect of Sr addition

Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia

A case report of congenital insensitivity to pain and anhidrosis

A novel, missense, mutation (P81R) in the TRH receptor gene in congenital central hypothyroidism

A novel, missense, mutation (P81R) in the TRH receptor gene in congenital central hypothyroidism

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