الأبحاث

محمد السيد محمد الأسرج

مدرس

كلية العلوم علم الحيوان

Meta‐analysis of the demographic and prognostic significance of gastrointestinal symptoms in COVID‐19 patients

Wiley Publishing Asia Pty Ltd 2022

Patient derived organoids confirm that PI3K/AKT signalling is an escape pathway for radioresistance and a target for therapy in rectal cancer

Frontiers 2022

Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa

Emory University 2022

New missense variants in RELT causing hypomineralised amelogenesis imperfecta

Blackwell Publishing Ltd 2020

البحث الكامل الملخص

LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

Elsevier 2019

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes

1-16 2018

The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5

Nature Portfolio 2018

البحث الكامل الملخص

Use of a gene-based case-control association approach in exome sequencing data to elucidate the molecular basis of a mendelian phenotype

2017

Use of a gene-based case-control association approach in exome sequencing data to elucidate the molecular basis of a mendelian phenotype

2017

Homozygous Single Base Deletion in TUSC3 Causes Intellectual Disability with Developmental Delay in an Omani Family

! 2016 Wiley Periodicals, Inc. 2016

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Human Genetics

Molecular Biology

Ophthalmology

Zoology