X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (419) 419
Publication (34) 34
Conference Proceeding (14) 14
Book Chapter (5) 5
Dissertation (5) 5
Book / eBook (4) 4
Book Review (2) 2
Government Document (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
hbf (252) 252
humans (183) 183
hematology (120) 120
index medicus (116) 116
female (93) 93
adult (82) 82
male (76) 76
hemoglobin (66) 66
fetal hemoglobin (62) 62
thalassemia (57) 57
beta-thalassemia (56) 56
fetal hemoglobin - genetics (55) 55
hydroxyurea (50) 50
adolescent (47) 47
expression (46) 46
beta-thalassemia - genetics (44) 44
child (44) 44
fetal hemoglobin - analysis (41) 41
fetal hemoglobin - metabolism (41) 41
mutation (40) 40
sickle cell anemia (40) 40
hemic and lymphatic diseases (39) 39
anemia (38) 38
sickle cell disease (38) 38
biochemistry & molecular biology (34) 34
child, preschool (34) 34
fetal-hemoglobin (34) 34
disease (33) 33
middle aged (33) 33
bcl11a (31) 31
haplotypes (31) 31
β-thalassemia (31) 31
anemia, sickle cell - genetics (27) 27
hereditary persistence (25) 25
phenotype (24) 24
globins - genetics (23) 23
pregnancy (23) 23
anemia, sickle cell - blood (21) 21
animals (21) 21
flow cytometry (21) 21
infant (21) 21
polymorphism, single nucleotide (21) 21
beta-thalassemia - blood (20) 20
genetics & heredity (20) 20
genome-wide association (20) 20
genotype (20) 20
hba (20) 20
hbf induction (20) 20
hbs1l-myb (20) 20
young adult (20) 20
analysis (19) 19
oncology (19) 19
medicine, research & experimental (18) 18
pediatrics (18) 18
sickle-cell-anemia (18) 18
aged (17) 17
children (17) 17
congenital, hereditary, and neonatal diseases and abnormalities (17) 17
erythropoiesis (17) 17
fetuses (17) 17
gamma-globins - genetics (17) 17
globin (17) 17
hydroxyurea - therapeutic use (17) 17
alpha-thalassemia (16) 16
anemia, sickle cell - drug therapy (16) 16
beta-globins - genetics (16) 16
carrier proteins - genetics (16) 16
gene (16) 16
gene expression (16) 16
haplotype (16) 16
hbf levels (16) 16
medical laboratory technology (16) 16
fetal hemoglobin - biosynthesis (15) 15
nuclear proteins - genetics (15) 15
sio (15) 15
alleles (14) 14
beta-thalassemia - drug therapy (14) 14
f-cells (14) 14
gene therapy (14) 14
heterozygote (14) 14
infant, newborn (14) 14
engineering, electrical & electronic (13) 13
erythrocytes (13) 13
medicine (13) 13
adults (12) 12
genetic aspects (12) 12
hbf4-sio2 (12) 12
homozygote (12) 12
hplc (12) 12
hydroxyurea - administration & dosage (12) 12
medicine & public health (12) 12
original (12) 12
sickle-cell-disease (12) 12
thalassemia - blood (12) 12
base sequence (11) 11
cells, cultured (11) 11
chromatography, high pressure liquid (11) 11
fetal-hemoglobin levels (11) 11
hemoglobinopathy (11) 11
intermedia (11) 11
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (423) 423
Japanese (5) 5
Turkish (4) 4
Chinese (3) 3
German (3) 3
Italian (2) 2
French (1) 1
Korean (1) 1
Persian (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Clinical Biochemistry, ISSN 0009-9120, 03/2019, Volume 65, pp. 24 - 28
Objective: The aims of this study were to establish the reference intervals for HbA2 and HbF in a Guizhou population of reproductive age, and to determine the... 
Cut-off value | Reference interval | HbF | HbA | β-thalassemia
Journal Article
Clinical Chemistry and Laboratory Medicine, ISSN 1434-6621, 08/2018, Volume 56, Issue 9, pp. 1507 - 1513
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 2008, Volume 49, Issue 27, pp. 4272 - 4275
HBF 4–SiO 2 efficiently catalyses the thia-Michael addition to α,β-unsaturated carbonyl compounds and finds application in the one-pot synthesis of... 
Heterogeneous catalyst | Thiol | α,β-Unsaturated carbonyl | HBF 4–SiO 2 | Benzothiazepines | Thia-Michael addition | SiO | HBF | HBF4-SiO2 | thiol | HCLO4-SIO2 | CHEMISTRY, ORGANIC | GREEN | SOLVENT | MERCAPTANS | heterogeneous catalyst | EPOXIDE RINGS | THIOLS | KETONES | alpha,beta-unsaturated carbonyl | benzothiazepines | 1,4-ADDITION | thia-Michael addition | CONJUGATE ADDITION | MAGNESIUM PERCHLORATE
Journal Article
Materials Letters, ISSN 0167-577X, 06/2015, Volume 157, pp. 53 - 56
Abstract A simple approach is explored to synthesize orthorhombic MoO 3 (α-MoO 3 ) nanobelts using sodium molybdate (Na 2 MoO 4 ) and fluoboric acid (HBF 4 ).... 
h-MoO 3 nanorods | Adsorption | HBF 4 | α-MoO 3 nanobelts | Formation mechanism
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 05/2010, Volume 51, Issue 21, pp. 2872 - 2874
The synthesis of symmetrical 2,6-disubstituted 4-fluorotetrahydropyran derivatives has been achieved using HBF ·OEt via a tandem allylation and Prins... 
4-Fluorotetrahydropyrans | Diastereoselective | HBF | Allyltrimethylsilane | OEt | Prins cyclization
Journal Article
by Han, WP and Huang, L and Li, YY and Han, YY and Li, D and An, BQ and Huang, SW
CLINICAL BIOCHEMISTRY, ISSN 0009-9120, 03/2019, Volume 65, pp. 24 - 28
Objective: The aims of this study were to establish the reference intervals for HbA(2 ) and HbF in a Guizhou population of reproductive age, and to determine... 
HbA | Cut-off value | Reference interval | MEDICAL LABORATORY TECHNOLOGY | beta-thalassemia | HbF
Journal Article
American journal of hematology, ISSN 0361-8609, 11/2016, Volume 91, Issue 11, pp. 1118 - 1122
Fetal hemoglobin (HbF) levels are higher in the Arab-Indian (AI) β-globin gene haplotype of sickle cell anemia compared with African-origin haplotypes. To... 
whole genome sequencing | RNA sequencing | erythroid progenitors | ANTXR1 | HbF
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 03/2019, Volume 65, pp. 24 - 28
The aims of this study were to establish the reference intervals for HbA2 and HbF in a Guizhou population of reproductive age, and to determine the cut-off... 
HbA2 | Cut-off value | Reference interval | HbF | β-thalassemia
Journal Article
Acta Haematologica Polonica, ISSN 0001-5814, 2018, Volume 49, Issue 1, pp. 1 - 8
Journal Article
Applied Organometallic Chemistry, ISSN 0268-2605, 03/2019, Volume 33, Issue 3
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 09/2010, Volume 51, Issue 37, pp. 4827 - 4829
A variety of alkenes undergo smooth amidation with nitriles in the presence of HBF ·OEt at room temperature under mild conditions to afford the corresponding... 
α-Aryl ethyl amides | Nitriles | Ritter amidation | Alkenes | HBF | OEt
Journal Article
Hematology, ISSN 1024-5332, 03/2016, pp. 1 - 5
Fetal hemoglobin (HbF) modulates the phenotype of sickle cell anemia (SCA) by inhibiting deoxy sickle hemoglobin (HbS) polymerization. HbF genes are... 
HbF | Sickle cell anemia | BCL11A gene
Journal Article
Journal of Biomolecular Structure and Dynamics, ISSN 0739-1102, 2019, Volume 37, Issue 14, pp. 3848 - 3857
Journal Article
Iranian Biomedical Journal, ISSN 1028-852X, 07/2015, Volume 19, Issue 3, pp. 177 - 182
Journal Article
Blood, ISSN 0006-4971, 03/2011, Volume 117, Issue 12, pp. 3435 - 3444
With the aim of finding small molecules that stimulate erythropoiesis earlier than erythropoietin and that enhance erythroid colony-forming unit (CFU-E)... 
HBF REACTIVATION | FETAL-HEMOGLOBIN | DIAMOND-BLACKFAN ANEMIA | GENE-EXPRESSION | C-KIT | RECEPTOR | CFU-E | HYPOXIA | HEMATOLOGY | KIT-LIGAND | ERYTHROID PROGENITORS | Red Cells, Iron, and Erythropoiesis
Journal Article
HAEMATOLOGICA, ISSN 0390-6078, 08/2019, Volume 104, Issue 9, pp. 1720 - 1730
The complex, frequently devastating, multi-organ pathophysiology of sickle cell disease has a single root cause: polymerization of deoxygenated sickle... 
IN-VITRO | RISK-FACTORS | GAMMA-GLOBIN SYNTHESIS | DNA-DAMAGE | GENE-EXPRESSION | SUBCUTANEOUS DECITABINE | HBF INDUCTION | HEREDITARY PERSISTENCE | HISTONE DEACETYLASE INHIBITORS | HEMATOLOGY | FETAL-HEMOGLOBIN-SYNTHESIS | Review
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.