Computational approaches for discovering significant microRNAs, microRNA-mRNA regulatory pathways, and therapeutic protein targets in endometrial cancer.

Autor: Ajabnoor G; Department of Clinical Biochemistry, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Alsubhi F; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Shinawi T; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia., Habhab W; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Albaqami WF; Department of Science, Prince Sultan Military College of Health Sciences, Dhahran, Saudi Arabia., Alqahtani HS; Department of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dammam, Saudi Arabia., Nasief H; Department of Obstetrics and Gynecology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Bondagji N; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Obstetrics and Gynecology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Elango R; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Shaik NA; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Banaganapalli B; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.

Publikováno v: Frontiers in genetics [Front Genet] 2023 Jan 10; Vol. 13, pp. 1105173. Date of Electronic Publication: 2023 Jan 10 (Print Publication: 2022).

Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches.

Autor: Sahly NN; Department of Obstetrics and Gynecology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Banaganapalli B; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Sahly AN; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Jeddah, Saudi Arabia., Aligiraigri AH; Department of Hematology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Nasser KK; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia., Shinawi T; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia., Mohammed A; Department of Biology, College of Science, University of Jeddah, Jeddah, Saudi Arabia., Alamri AS; Department of Clinical Laboratories Sciences, College of Applied Medical Sciences, Taif University, Taif, Saudi Arabia.; Centre of Biomedical Sciences Research (CBSR), Deanship of Scientific Research, Taif University, Saudi Arabia., Bondagji N; Department of Obstetrics and Gynecology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Elango R; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Shaik NA; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.

Publikováno v: Systems biology in reproductive medicine [Syst Biol Reprod Med] 2021 Jun; Vol. 67 (3), pp. 209-220. Date of Electronic Publication: 2021 Mar 08.

Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women.

Autor: Ajabnoor GMA; Department of Clinical Biochemistry, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Mohammed NA; Department of Clinical Biochemistry, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Banaganapalli B; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Abdullah LS; Department of Pathology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Bondagji ON; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Mansouri N; Department of Gynecology and Obstetrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Sahly NN; Department of Gynecology and Obstetrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Vaidyanathan V; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Bondagji N; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Gynecology and Obstetrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Elango R; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Shaik NA; Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.

Publikováno v: Frontiers in genetics [Front Genet] 2018 Dec 14; Vol. 9, pp. 552. Date of Electronic Publication: 2018 Dec 14 (Print Publication: 2018).

Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent‐reported measures.

Autor: Alrayes, Nuha^1,2 (AUTHOR) nalrayes@kau.edu.sa, Issa, Noha M.^3,4 (AUTHOR), Alghubayshi, Omar Y.⁵ (AUTHOR), Al‐Amaa, Jumana Y.^2,3 (AUTHOR), Alsabban, Ashwaq Hassan⁶ (AUTHOR), Al Shaer, Dalal Sameer³ (AUTHOR), Alyoubi, Reem Abdullah⁷ (AUTHOR), Nasser, Khalidah K.^1,2 (AUTHOR), Alkhiary, Yaser M.⁸ (AUTHOR)

Publikováno v: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-20. 20p.

Histopathological Patterns of Testicular Biopsy in Male Infertile Patients: A Cross-sectional Study.

Autor: VEERAMACHANENI, LEELA RANI¹ l_gopikonda@yahoo.com, THIRUKOVELA, JAGDISH², GOSAIN, RATNA³, KATE, MADHURI SHREESH⁴, GOPIKONDA, SHREYA SRI⁵

Publikováno v: Journal of Clinical & Diagnostic Research. Dec2023, Vol. 17 Issue 12, p16-19. 4p.