Beta-lactamase-negative ampicillin-resistant Haemophilus influenzae type b meningitis in partially immunized immunocompetent child: a case report

por Qureshi, Majid Ali, Asad, Imran, Chaudhary, Adeel, Abuhammour, Walid
Publicado 2021

Array Comparative Genomic hybridization of breast cancer in the kingdom of Saudi Arabia

por Al-Harbi, Lina, Shokry, Ahmed, Sabir, Jamal, Chaudhary, Adeel, Dallol, Ashraf
Publicado 2014

Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly

por Imran Naseer, Muhammad, Abdulrahman Abdulkareem, Angham, Yousef Muthaffar, Osama, Chaudhary, Adeel G.
Publicado 2021

MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia

por Batarfi, Asma A., Filimban, Najlaa, Bajouh, Osama S., Dallol, Ashraf, Chaudhary, Adeel G., Bakhashab, Sherin
Publicado 2019

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and In...

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Pushparaj, Peter Natesan, Bibi, Fehmida, Chaudhary, Adeel G.
Publicado 2020

Oxidative stress and hepatitis C virus

por Paracha, Usman Zafar, Fatima, Kaneez, Alqahtani, Mohammad, Chaudhary, Adeel, Abuzenadah, Adel, Damanhouri, Ghazi, Qadri, Ishtiaq
Publicado 2013

Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi A...

por Hussein, Ibtessam Ramzi, Chaudhary, Adeel G, Bassiouni, Randa, AlQuaiti, Maha, Sogaty, Samira, Al-Qahtani, Mohammed
Publicado 2014

Sunitinib effectively reduces clonogenic acute myeloid leukemia cells in vitro

por Ahmed, Farid, Al-Oteibi, Manal, Layati, Samah, Kadi, Fatima, Chaudhary, Adeel, Gari, Mamdooh, Al-Qahtani, Mohammed
Publicado 2014

Assessment of Radiation Induced Therapeutic Effect and Cytotoxicity in Cancer Patients Based on Transcriptomic Profiling

por Karim, Sajjad, Mirza, Zeenat, Chaudhary, Adeel G., Abuzenadah, Adel M., Gari, Mamdooh, Al-Qahtani, Mohammed H.
Publicado 2016

KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring

por Homma, Noriko, Zhou, Ruyun, Naseer, Muhammad Imran, Chaudhary, Adeel G, Al-Qahtani, Mohammed H, Hirokawa, Nobutaka
Publicado 2018

Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Jan, Mohammed Mohammed, Chaudhary, Adeel G., Al-Qahtani, Mohammad H.
Publicado 2020

Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia

por Alharazy, Shatha, Naseer, Muhammad Imran, Alissa, Eman, Robertson, Margaret Denise, Lanham-New, Susan, Chaudhary, Adeel G.
Publicado 2021

Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia

por Alharazy, Shatha, Alissa, Eman, Lanham-New, Susan, Naseer, Muhammad Imran, Chaudhary, Adeel G., Robertson, M Denise
Publicado 2021

Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia

por Alharazy, Shatha, Robertson, M Denise, Lanham-New, Susan, Naseer, Muhammad Imran, Chaudhary, Adeel G, Alissa, Eman
Publicado 2021

Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability

por Karim, Sajjad, Hussein, Ibtessam Ramzi, Schulten, Hans-Juergen, Alsaedi, Saad, Mirza, Zeenat, Al-Qahtani, Mohammed, Chaudhary, Adeel
Publicado 2023

Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia

por Naseer, Muhammad Imran, Faheem, Muhammad, Al-Quaiti, Maha Mohsin, Chaudhary, Adeel G, Hirokawa, Nobutaka, Al-Qahtani, Mohammed H
Publicado 2014

Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family

por Naseer, Muhammad Imran, Rasool, Mahmood, Abdulkareem, Angham Abdulrahman, Chaudhary, Adeel G., Zaidi, Syed Kashif, Al-Qahtani, Mohammad H.
Publicado 2019

Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic...

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Jan, Mohammed M., Chaudhary, Adeel G., Alharazy, Shatha, AlQahtani, Mohammad H.
Publicado 2020

Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Muthaffar, Osama Yousef, Sogaty, Sameera, Alkhatabi, Hiba, Almaghrabi, Sarah, Chaudhary, Adeel G.
Publicado 2021

Molecular docking of resveratrol with known protein structures as well as high-throughput meta-data analyses uncork the “French Paradox” and its potential “Druggable” targets in hu...

por Pushparaj, Peter Natesan, Mirza, Zeenat, Karim, Sajjad, Gauthaman, Kalamegam, Narasimhan, Kothandaraman, Abuzenadah, Adel, Gari, Mamdooh, Chaudhary, Adeel, Alqahtani, Mohammed
Publicado 2014