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American Journal of Hematology
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May 18, 2016
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia
Vinod Vathipadiekal, Abdulrahman Alsultan, Kristin Baltrusaitis, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Marlene Tejeda, John J Farrell, Congcong Zhu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Bilcag Akgun, Seung Hoan Choi, John J Farrell, et al.
American Journal of Hematology
|
May 30, 2012
A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype
Abdulrahman Alsultan, Duyen A Ngo, John J Farrell, et al.
Blood Cells, Molecules & Diseases
|
June 11, 2016
Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia
Elmutaz M Shaikho, Alawi H Habara, Abdulrahman Alsultan, et al.
Genome Research
|
February 25, 2022
An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns
Bowen Jin, John A Capra, Penelope Benchek, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
September 29, 2022
Transmission of Carbapenem-Resistant Klebsiella pneumoniae in US Hospitals
Courtney L Luterbach, Liang Chen, Lauren Komarow, et al.
Blood Cells, Molecules & Diseases
|
March 8, 2013
Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype
Duyen Ngo, Harold Bae, Martin H Steinberg, et al.
Life Science Alliance
|
February 28, 2024
A comparative study of structural variant calling in WGS from Alzheimer's disease families
John S Malamon, John J Farrell, Li Charlie Xia, et al.
British Journal of Haematology
|
January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes
Zhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 76) with videos related to
Sort By:
Page
of 8
American Journal of Hematology
|
May 18, 2016
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia
Vinod Vathipadiekal, Abdulrahman Alsultan, Kristin Baltrusaitis, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Marlene Tejeda, John J Farrell, Congcong Zhu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Basic Science and Pathogenesis
Bilcag Akgun, Seung Hoan Choi, John J Farrell, et al.
American Journal of Hematology
|
May 30, 2012
A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype
Abdulrahman Alsultan, Duyen A Ngo, John J Farrell, et al.
Blood Cells, Molecules & Diseases
|
June 11, 2016
Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia
Elmutaz M Shaikho, Alawi H Habara, Abdulrahman Alsultan, et al.
Genome Research
|
February 25, 2022
An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns
Bowen Jin, John A Capra, Penelope Benchek, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
September 29, 2022
Transmission of Carbapenem-Resistant Klebsiella pneumoniae in US Hospitals
Courtney L Luterbach, Liang Chen, Lauren Komarow, et al.
Blood Cells, Molecules & Diseases
|
March 8, 2013
Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype
Duyen Ngo, Harold Bae, Martin H Steinberg, et al.
Life Science Alliance
|
February 28, 2024
A comparative study of structural variant calling in WGS from Alzheimer's disease families
John S Malamon, John J Farrell, Li Charlie Xia, et al.
British Journal of Haematology
|
January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes
Zhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Page
of 8