X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (17) 17
mutation (10) 10
genes (9) 9
humans (9) 9
saudi arabia (9) 9
thalassemia (9) 9
mutations (8) 8
genetic aspects (7) 7
hemoglobin (7) 7
beta-thalassemia - genetics (6) 6
female (6) 6
male (6) 6
population (6) 6
proteins (6) 6
alpha-globins - genetics (5) 5
alpha-thalassemia - genetics (5) 5
amino acids (5) 5
biochemistry & molecular biology (5) 5
bioinformatics (5) 5
gene (5) 5
medicine (5) 5
polymorphism (5) 5
single-nucleotide polymorphism (5) 5
analysis (4) 4
biotechnology & applied microbiology (4) 4
genetic research (4) 4
genetics (4) 4
globin genes (4) 4
identification (4) 4
medicine, general & internal (4) 4
prevalence (4) 4
research (4) 4
saudi population (4) 4
sickle-cell-disease (4) 4
single nucleotide polymorphisms (4) 4
studies (4) 4
susceptibility (4) 4
adolescent (3) 3
adult (3) 3
allele (3) 3
alleles (3) 3
arabia (3) 3
beta-thalassemia (3) 3
biology (3) 3
biology and life sciences (3) 3
blood transfusion (3) 3
care and treatment (3) 3
child (3) 3
deoxyribonucleic acid--dna (3) 3
dna (3) 3
dna sequencing (3) 3
eastern province (3) 3
engineering, biomedical (3) 3
gene mutations (3) 3
genetics & heredity (3) 3
genome-wide association (3) 3
genotype (3) 3
haplotypes (3) 3
health aspects (3) 3
hematology (3) 3
hemoglobin a (3) 3
heterozygote (3) 3
homozygote (3) 3
introns (3) 3
medicine, research & experimental (3) 3
metarhizium anisopliae (3) 3
microbiology (3) 3
molecular sequence data (3) 3
multidisciplinary sciences (3) 3
polymorphism, single nucleotide (3) 3
research and analysis methods (3) 3
research article (3) 3
review (3) 3
rna interference (3) 3
saudi arabia - epidemiology (3) 3
sickle cell anemia (3) 3
sickle cell disease (3) 3
spectrum (3) 3
structure-function relationships (3) 3
swiss-model (3) 3
web server (3) 3
alpha (2) 2
alpha-thalassemia (2) 2
alpha-thalassemia - epidemiology (2) 2
alpha-thalassemia - pathology (2) 2
animals (2) 2
bacteria (2) 2
base sequence (2) 2
bcl11a (2) 2
beta-globins - genetics (2) 2
beta-thalassemia - epidemiology (2) 2
beta-thalassemia - pathology (2) 2
beta-thalassemia - therapy (2) 2
beta-thalassemia patients (2) 2
biochemistry (2) 2
biosynthesis (2) 2
borderline hba (2) 2
cardiovascular disease (2) 2
carriers (2) 2
case-control studies (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 10/2017, Volume 12, Issue 10, p. e0185270
Recent studies on the variants in duplicated human alpha globin genes (HBA2 and HBA1) actively target the [alpha]-globin gene as molecular modulators for the... 
Usage | Genetic variation | Physiological aspects | Hemoglobin | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2017, Volume 12, Issue 10, pp. e0185270 - e0185270
Journal Article
BioMed Research International, ISSN 2314-6133, 01/2017, Volume 2017
  Background and Objectives. β-Thalassemia and sickle cell disease are genetic disorders characterized by reduced and abnormal β-globin chain production,... 
Thalassemia | Genotype | Care and treatment | Genetic aspects | Sickle cell anemia | Research | Haplotypes | Hospitals | Sickle cell disease | Genes | Colleges & universities | Children & youth
Journal Article
PLoS ONE, 01/2016, Volume 11, Issue 1
Background [alpha] -Thalassemia ([alpha] -thal) is a genetic disorder caused by the substitution of single amino acid or large deletions in the HBA1 and/or... 
Journal Article
Archives of medical science : AMS, ISSN 1734-1922, 01/2018, Volume 14, Issue 1, p. 230
Elevated HbA (hemoglobin A ) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However, some carriers... 
Journal Article
Journal Article
Current medical research and opinion, 02/2018, p. 1
Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A (HbA ) levels, which is found at low levels (<3%) in... 
Journal Article
Journal of Biopesticides, ISSN 0974-391X, 2010, Volume 3, Issue 1, pp. 386 - 393
Journal Article
Journal Article
Journal Article
Microbial Pathogenesis, ISSN 0882-4010, 03/2018, Volume 116, pp. 351 - 355
Journal Article
Artificial Cells, Nanomedicine, and Biotechnology, ISSN 2169-1401, 12/2019, Volume 47, Issue 1, pp. 2072 - 2082
The establishment of a benign system for the nanoparticle (NPs) synthesis, is a key in nanotechnology for the environmental and health care industries.... 
zinc NPs | Phoenix dactylifera; thermophile | Bacillus haynesii | Antibacterial | green synthesis | BACTERIA | MATERIALS SCIENCE, BIOMATERIALS | ENGINEERING, BIOMEDICAL | ZINC-OXIDE | NANOCRYSTALS | thermophile | SILVER NANOPARTICLES | ANTIBACTERIAL ACTIVITY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | Phoenix dactylifera | BIOSYNTHESIS | SKIN | NANOTECHNOLOGY
Journal Article
Current Medical Research and Opinion, ISSN 0300-7995, 05/2018, Volume 34, Issue 5, pp. 945 - 951
Introduction: Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A 2 (HbA 2 ) levels, which is found at low... 
Hemoglobin A | Globin genes | Molecular diagnosis | Borderline HbA | HbA | β-Thalassemia carriers | β-Thalassemia trait | Mutation | Pre-marital screening
Journal Article
International Journal of Nephrology, ISSN 2090-214X, 01/2019, Volume 2019
Background. End-stage renal disease (ESRD) is the result of hypertensive nephrosclerosis and chronic glomerular diseases and is associated with high morbidity... 
Hypertension | Haplotypes | Pediatrics | Nephrology | African Americans | Cardiovascular disease | Epidemiology | Studies | Population | Genetics | Diabetes | Kidney diseases | Bioinformatics | Chromosomes | Polymorphism
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 06/2015, Volume 55, Issue 1, pp. 27 - 29
Journal Article