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Association mapping validates previously identified quantitative trait loci for salt tolerance in rice (Oryza sativa L.)

Molecular breeding, 2016-12, Vol.36 (12), p.1-12, Article 172

2016

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The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes

Journal of the American Society of Nephrology, 2018-08, Vol.29 (8), p.2110-2122

2018

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Mutations of KIF14 cause primary microcephaly by impairing cytokinesis

Annals of neurology, 2017-10, Vol.82 (4), p.562-577

2017

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A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family

Annals of human genetics, 2018-05, Vol.82 (3), p.171-176

2018

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A Comparison of Machine Learning Methods for the Diagnosis of Motor Faults Using Automated Spectral Feature Extraction Technique

Journal of nondestructive evaluation, 2022-06, Vol.41 (2), Article 31

2022

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Role of 1-MCP in regulating ‘Kensington Pride’ mango fruit softening and ripening

Plant growth regulation, 2016-04, Vol.78 (3), p.401-411

2016

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65 Impact of baseline anaemia on clinical outcomes following percutaneous coronary intervention in stable and acute coronary artery disease: a single centre retrospective study

Heart (British Cardiac Society), 2024-06, Vol.110 (Suppl 3), p.73-73

2024

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Charged Particles pT Spectra and the Correlation between pT and all Charged Particles at √S = 900 GeV

International journal of theoretical physics, 2019-06, Vol.58 (6), p.2027-2032

2019

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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.108-125

2020

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Identification of Environmental Compounds That May Trigger Early Female Puberty by Activating Human GnRHR and KISS1R

Endocrinology (Philadelphia), 2024-08, Vol.165 (10)

2024

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307.2: Bioprinted Immune-protective Islet-containing Tissues Successfully Regulate Blood Glucose in Rodent Models of Type 1 Diabetes

Transplantation, 2021-12, Vol.105 (12 Suppl 2), p.S23-S23

2021

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Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Genetics in medicine, 2024-04, Vol.26 (4), p.101057, Article 101057

2024

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TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

Human molecular genetics, 2020-08, Vol.29 (14), p.2435-2450

2020

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A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees

American journal of medical genetics. Part A, 2022-02, Vol.188 (2), p.498-508

2022

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Straddling interatrial embolus: a rare clinical dilemma

BMJ case reports, 2016-06, Vol.2016, p.bcr2016215136

2016

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The study of light nuclei production in different interactions at 4.2 AGeV/c

Canadian journal of physics, 2016-07, Vol.94 (7), p.693-696

2016

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A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.556-558

2018

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Efficacy of Sodium-Glucose Cotransporter-2 inhibitors in heart failure patients treated with dual angiotensin receptor blocker-neprilysin inhibitor: An updated meta-analysis

Annals of medicine and surgery, 2021-10, Vol.70, p.102796-102796, Article 102796

2021

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Electronic cigarettes: a perspective for the primary care physician

Southern medical journal (Birmingham, Ala.), 2014-10, Vol.107 (10), p.630-632

2014

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Eric E. Ekembe, Lauren Harvey and Eric Dwyer (eds): Interface between English Language Education Policies and Practice: Examples from Various Contexts: Palgrave MacMillan Cham, 2022, xix + 300 pp, USD 139.99 ISBN 978-3-031-14309-0

Language Policy, 2024, Vol.23 (2), p.221-223

Khan, Muhammad Kamal

2024

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Genetics of human Bardet-Biedl syndrome, an updates

Clinical genetics, 2016-07, Vol.90 (1), p.3-15

2016

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Assessing growth performance, morphometric traits, meat chemical composition and cholesterol content in four phenotypes of naked neck chicken

Poultry science, 2022-03, Vol.101 (3), p.101667-101667, Article 101667

2022

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Beneficial Effects of Statins on the Rates of Hepatic Fibrosis, Hepatic Decompensation, and Mortality in Chronic Liver Disease: A Systematic Review and Meta-Analysis

The American journal of gastroenterology, 2017-10, Vol.112 (10), p.1495-1505

2017

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Glutathione (GSH) improves sperm quality and testicular morphology in streptozotocin-induced diabetic mice

Asian journal of andrology, 2021-05, Vol.23 (3), p.281-287

2021

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Association mapping validates previously identified quantitative trait loci for salt tolerance in rice (Oryza sativa L.)

The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes

Mutations of KIF14 cause primary microcephaly by impairing cytokinesis

A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family

A Comparison of Machine Learning Methods for the Diagnosis of Motor Faults Using Automated Spectral Feature Extraction Technique

Role of 1-MCP in regulating ‘Kensington Pride’ mango fruit softening and ripening

65 Impact of baseline anaemia on clinical outcomes following percutaneous coronary intervention in stable and acute coronary artery disease: a single centre retrospective study

Charged Particles pT Spectra and the Correlation between pT and all Charged Particles at √S = 900 GeV

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Identification of Environmental Compounds That May Trigger Early Female Puberty by Activating Human GnRHR and KISS1R

307.2: Bioprinted Immune-protective Islet-containing Tissues Successfully Regulate Blood Glucose in Rodent Models of Type 1 Diabetes

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees

Straddling interatrial embolus: a rare clinical dilemma

The study of light nuclei production in different interactions at 4.2 AGeV/c

A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

Efficacy of Sodium-Glucose Cotransporter-2 inhibitors in heart failure patients treated with dual angiotensin receptor blocker-neprilysin inhibitor: An updated meta-analysis

Electronic cigarettes: a perspective for the primary care physician

Eric E. Ekembe, Lauren Harvey and Eric Dwyer (eds): Interface between English Language Education Policies and Practice: Examples from Various Contexts: Palgrave MacMillan Cham, 2022, xix + 300 pp, USD 139.99 ISBN 978-3-031-14309-0

Genetics of human Bardet-Biedl syndrome, an updates

Assessing growth performance, morphometric traits, meat chemical composition and cholesterol content in four phenotypes of naked neck chicken

Beneficial Effects of Statins on the Rates of Hepatic Fibrosis, Hepatic Decompensation, and Mortality in Chronic Liver Disease: A Systematic Review and Meta-Analysis

Glutathione (GSH) improves sperm quality and testicular morphology in streptozotocin-induced diabetic mice

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