Search research articles
Contact Us
Filters
Showing results (931-940 of 1,192) with videos related to
Page
of 120
Sort By:
Hemoglobin
|
May 2, 2019
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study
Alexandra 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 telangiectasia
Bassam 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 Emiratis
Charu 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 Trial
Shahla 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 mice
K 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 inhibitor
M 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 cancer
H 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 gene
F 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 vectors
Mei 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 stature
Sally Badawi, Divya Saro Varghese, Anjana Raj, et al.
Page
of 120
Search research articles
Search
Showing results (931-940 of 1,192) with videos related to
Sort By:
Page
of 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 Study
Alexandra 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 telangiectasia
Bassam 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 Emiratis
Charu 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 Trial
Shahla 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 mice
K 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 inhibitor
M 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 cancer
H 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 gene
F 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 vectors
Mei 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 stature
Sally Badawi, Divya Saro Varghese, Anjana Raj, et al.
Page
of 120