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R Ali

Showing results (931-940 of 1,192) with videos related to

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Hemoglobin|May 2, 2019
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort StudyAlexandra Kolliopoulou, Stavroula Siamoglou, Anne John, et al.
Plos One|October 25, 2011
Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasiaBassam R Ali, Imen Ben-Rebeh, Anne John, et al.
Annals of Human Genetics|September 24, 2020
Association of variants in PTPN22, CTLA-4, IL2-RA, and INS genes with type 1 diabetes in EmiratisCharu Sharma, Bassam R Ali, Wael Osman, et al.
Cureus|January 8, 2025
Tranexamic Acid in Pregnant Women With Placenta Previa: A Double-Blind, Multicenter Randomized Clinical TrialShahla Alalaf, Ariana K Jawad, Namir G Al-Tawil, et al.
Gene Therapy|November 25, 2011
Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient miceK S Balaggan, Y Duran, A Georgiadis, et al.
Molecular Immunology|December 27, 2005
Biological and molecular docking studies on coagulin-H: Human IL-2 novel natural inhibitorM Ahmed Mesaik, Zaheer-Ul-Haq, Shahnaz Murad, et al.
British Journal of Cancer|January 19, 2013
Astronomical algorithms for automated analysis of tissue protein expression in breast cancerH R Ali, M Irwin, L Morris, et al.
The British Journal of Dermatology|October 31, 2012
An investigation of rheumatoid arthritis loci in patients with early-onset psoriasis validates association of the REL geneF R Ali, A Barton, R L I Smith, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Frontiers in Cell and Developmental Biology|December 11, 2023
Unveiling the pathogenic mechanisms of NPR2 missense variants: insights into the genotype-associated severity in acromesomelic dysplasia and short statureSally Badawi, Divya Saro Varghese, Anjana Raj, et al.
Pageof 120

Showing results (931-940 of 1,192) with videos related to

Sort By:
Pageof 120
Hemoglobin|May 2, 2019
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort StudyAlexandra Kolliopoulou, Stavroula Siamoglou, Anne John, et al.
Plos One|October 25, 2011
Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasiaBassam R Ali, Imen Ben-Rebeh, Anne John, et al.
Annals of Human Genetics|September 24, 2020
Association of variants in PTPN22, CTLA-4, IL2-RA, and INS genes with type 1 diabetes in EmiratisCharu Sharma, Bassam R Ali, Wael Osman, et al.
Cureus|January 8, 2025
Tranexamic Acid in Pregnant Women With Placenta Previa: A Double-Blind, Multicenter Randomized Clinical TrialShahla Alalaf, Ariana K Jawad, Namir G Al-Tawil, et al.
Gene Therapy|November 25, 2011
Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient miceK S Balaggan, Y Duran, A Georgiadis, et al.
Molecular Immunology|December 27, 2005
Biological and molecular docking studies on coagulin-H: Human IL-2 novel natural inhibitorM Ahmed Mesaik, Zaheer-Ul-Haq, Shahnaz Murad, et al.
British Journal of Cancer|January 19, 2013
Astronomical algorithms for automated analysis of tissue protein expression in breast cancerH R Ali, M Irwin, L Morris, et al.
The British Journal of Dermatology|October 31, 2012
An investigation of rheumatoid arthritis loci in patients with early-onset psoriasis validates association of the REL geneF R Ali, A Barton, R L I Smith, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Frontiers in Cell and Developmental Biology|December 11, 2023
Unveiling the pathogenic mechanisms of NPR2 missense variants: insights into the genotype-associated severity in acromesomelic dysplasia and short statureSally Badawi, Divya Saro Varghese, Anjana Raj, et al.
Pageof 120