Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bader Almuzzaini

Showing results (11-20 of 29) with videos related to

Pageof 3
Sort By:
European Journal of Medical Genetics|August 18, 2019
A classification system for split-hand/ foot malformation (SHFM): A proposal based on 3 pedigrees with WNT10B mutationsMalak A Al Ghamdi, Mohammad M Al-Qattan, Ali Hadadi, et al.
Scientific Reports|July 17, 2020
The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohortMaha Al Ammari, Mohammed AlBalwi, Khizra Sultana, et al.
European Journal of Clinical Pharmacology|July 23, 2020
Blood pressure-lowering activity of statins: a systematic literature review and meta-analysis of placebo-randomized controlled trialsJahad Alghamdi, Abdulziz Alqadi, Adel Alharf, et al.
Genes|September 28, 2021
Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation SequencingMamoon Rashid, Abdulrahman Alasiri, Mohammad A Al Balwi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 30, 2016
In β-actin knockouts, epigenetic reprogramming and rDNA transcription inactivation lead to growth and proliferation defectsBader Almuzzaini, Aishe A Sarshad, Aldwin S Rahmanto, et al.
Saudi Pharmaceutical Journal : SPJ : the Official Publication of the Saudi Pharmaceutical Society|May 3, 2024
Pharmacological p38 MAPK inhibitor SB203580 enhances AML stem cell line KG1a chemosensitivity to daunorubicin by promoting late apoptosis, cell growth arrest in S-phase, and miR-328-3p upregulationSara Bahattab, Ali Assiri, Yazeid Alhaidan, et al.
Genomics|May 22, 2021
Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type AMuhammad Umair, Oliva Palander, Muhammad Bilal, et al.
Annals of Clinical and Translational Neurology|May 21, 2020
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delayAbdulaziz Asiri, Essra Aloyouni, Muhammad Umair, et al.
Genome Medicine|October 29, 2017
Nuclear Wiskott-Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cellsNikolai V Kuznetsov, Bader Almuzzaini, Joanna S Kritikou, et al.
Plos One|May 5, 2022
Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profilingSabine Matou-Nasri, Maria Najdi, Nouran Abu AlSaud, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
European Journal of Medical Genetics|August 18, 2019
A classification system for split-hand/ foot malformation (SHFM): A proposal based on 3 pedigrees with WNT10B mutationsMalak A Al Ghamdi, Mohammad M Al-Qattan, Ali Hadadi, et al.
Scientific Reports|July 17, 2020
The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohortMaha Al Ammari, Mohammed AlBalwi, Khizra Sultana, et al.
European Journal of Clinical Pharmacology|July 23, 2020
Blood pressure-lowering activity of statins: a systematic literature review and meta-analysis of placebo-randomized controlled trialsJahad Alghamdi, Abdulziz Alqadi, Adel Alharf, et al.
Genes|September 28, 2021
Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation SequencingMamoon Rashid, Abdulrahman Alasiri, Mohammad A Al Balwi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 30, 2016
In β-actin knockouts, epigenetic reprogramming and rDNA transcription inactivation lead to growth and proliferation defectsBader Almuzzaini, Aishe A Sarshad, Aldwin S Rahmanto, et al.
Saudi Pharmaceutical Journal : SPJ : the Official Publication of the Saudi Pharmaceutical Society|May 3, 2024
Pharmacological p38 MAPK inhibitor SB203580 enhances AML stem cell line KG1a chemosensitivity to daunorubicin by promoting late apoptosis, cell growth arrest in S-phase, and miR-328-3p upregulationSara Bahattab, Ali Assiri, Yazeid Alhaidan, et al.
Genomics|May 22, 2021
Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type AMuhammad Umair, Oliva Palander, Muhammad Bilal, et al.
Annals of Clinical and Translational Neurology|May 21, 2020
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delayAbdulaziz Asiri, Essra Aloyouni, Muhammad Umair, et al.
Genome Medicine|October 29, 2017
Nuclear Wiskott-Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cellsNikolai V Kuznetsov, Bader Almuzzaini, Joanna S Kritikou, et al.
Plos One|May 5, 2022
Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profilingSabine Matou-Nasri, Maria Najdi, Nouran Abu AlSaud, et al.
Pageof 3