X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (7209) 7209
Publication (663) 663
Newsletter (178) 178
Book Chapter (41) 41
Book Review (33) 33
Newspaper Article (16) 16
Conference Proceeding (15) 15
Magazine Article (15) 15
Dissertation (5) 5
Book / eBook (1) 1
Reference (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (5801) 5801
female (2687) 2687
fetal hemoglobin (2349) 2349
fetal hemoglobin - analysis (2032) 2032
adult (1844) 1844
male (1843) 1843
hematology (1553) 1553
index medicus (1308) 1308
fetal hemoglobin - genetics (1185) 1185
pregnancy (1076) 1076
infant, newborn (1063) 1063
animals (1048) 1048
child (965) 965
adolescent (867) 867
globins - genetics (866) 866
fetal hemoglobin - biosynthesis (784) 784
fetal hemoglobin - metabolism (774) 774
fetal-hemoglobin (765) 765
child, preschool (685) 685
anemia, sickle cell - blood (653) 653
anemia (646) 646
hemoglobin (627) 627
sickle cell anemia (624) 624
middle aged (613) 613
infant (611) 611
hydroxyurea (563) 563
thalassemia - genetics (550) 550
biochemistry & molecular biology (532) 532
anemia, sickle cell - genetics (524) 524
thalassemia (523) 523
mutation (516) 516
sickle cell disease (471) 471
beta-thalassemia (458) 458
heterozygote (430) 430
hemoglobins (429) 429
beta-thalassemia - genetics (426) 426
thalassemia - blood (426) 426
disease (418) 418
mice (387) 387
hemoglobins - analysis (384) 384
erythropoiesis (381) 381
anemia, sickle cell - drug therapy (378) 378
genes (378) 378
expression (367) 367
hydroxyurea - therapeutic use (352) 352
phenotype (350) 350
hemic and lymphatic diseases (338) 338
base sequence (332) 332
hemoglobinopathies - genetics (316) 316
homozygote (307) 307
pediatrics (307) 307
research (301) 301
erythrocytes (300) 300
pedigree (298) 298
erythrocytes - metabolism (289) 289
globins - biosynthesis (286) 286
genotype (280) 280
medicine, research & experimental (266) 266
hemoglobins, abnormal - analysis (262) 262
aged (260) 260
blood (260) 260
genetics & heredity (259) 259
gene expression (255) 255
cells, cultured (253) 253
hereditary persistence (243) 243
molecular sequence data (241) 241
gene expression regulation (237) 237
children (236) 236
anemia, sickle cell - complications (235) 235
gestational age (231) 231
haplotypes (231) 231
oncology (231) 231
article (228) 228
hemoglobins - metabolism (226) 226
beta-thalassemia - blood (217) 217
blood transfusion (217) 217
oxygen - blood (217) 217
erythrocyte count (216) 216
sickle-cell-anemia (216) 216
research article (208) 208
hydrogen-ion concentration (206) 206
chromatography, high pressure liquid (205) 205
analysis (202) 202
hemoglobins, abnormal - genetics (200) 200
amino acid sequence (197) 197
hemoglobins - biosynthesis (196) 196
hemoglobin a - analysis (195) 195
multidisciplinary sciences (193) 193
alpha-thalassemia (191) 191
beta-globins - genetics (190) 190
blood protein electrophoresis (190) 190
electrophoresis (189) 189
young adult (188) 188
hemoglobin a2 - analysis (184) 184
dna (183) 183
medicine, general & internal (182) 182
promoter regions, genetic (179) 179
genetic aspects (175) 175
sickle-cell-disease (174) 174
age factors (170) 170
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6597) 6597
German (191) 191
French (154) 154
Italian (109) 109
Russian (98) 98
Spanish (65) 65
Japanese (59) 59
Polish (53) 53
Chinese (39) 39
Portuguese (18) 18
Czech (14) 14
Dutch (6) 6
Hungarian (6) 6
Turkish (6) 6
Slovak (5) 5
Swedish (5) 5
Bulgarian (4) 4
Romanian (4) 4
Danish (3) 3
Norwegian (3) 3
Croatian (2) 2
Hebrew (2) 2
Arabic (1) 1
Finnish (1) 1
Greek (1) 1
Korean (1) 1
Serbian (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


12/2010
Objective : Hemoglobin F augmentation is another approach to treat sickle cell disease (SCD). This study evaluates the efficacy and impact of Hydroxyurea (HU)... 
Sickle cell anemia | Hydroxyurea | Sickle cell disease | Fetal hemoglobin
Web Resource
BLOOD, ISSN 0006-4971, 10/2009, Volume 114, Issue 18, pp. 3935 - 3937
Sardinian beta-thalassemia patients all are homozygotes for the same null allele in the beta-globin gene, but the clinical manifestations are extremely... 
FETAL-HEMOGLOBIN LEVELS | BCL11A | PHENOTYPE | HBS1L-MYB | HEMATOLOGY
Journal Article
Blood, ISSN 0006-4971, 04/2019, Volume 133, Issue 17, pp. 1865 - 1875
New treatments directly targeting polymerization of sickle hemoglobin (HbS), the proximate event in the pathophysiology of sickle cell disease (SCD), are... 
HEREDITARY PERSISTENCE | HEMATOLOGY | GARDOS CHANNEL BLOCKER | HEMOLYSIS | GBT440 | FETAL-HEMOGLOBIN | 103 | Clinical Trials and Observations
Journal Article
by Brook A and Sneyd R and Gurung R
Heart, ISSN 1355-6037, 06/2017, Volume 103, Issue 11, p. A108
Journal Article
JOURNAL OF PERINATOLOGY, ISSN 0743-8346, 06/2018, Volume 38, Issue 6, pp. 693 - 695
Objective To assess the effect of blood transfusions in neonates on partial pressure of oxygen in arterial blood (PaO2), arterial hemoglobin oxygen saturation... 
OXYGEN-SATURATION | FETAL-HEMOGLOBIN | INFANTS | PEDIATRICS | OBSTETRICS & GYNECOLOGY
Journal Article
Meta Gene, ISSN 2214-5400, 02/2017, Volume 11, pp. 172 - 177
The aim of this study was to identify, in people with sickle cell anemia (SCA), adenosine deaminase ( ; c. 22G > A; rs73598374) polymorphism, and correlating... 
Adenosine | Hemoglobin S | Hydroxycarbamide | Fetal hemoglobin
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2015, Volume 24, Issue 1, pp. R102 - R110
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 08/2017, Volume 18, Issue 1
Increase of the expression of [gamma]-globin gene and high production of fetal hemoglobin (HbF) in [beta]-thalassemia patients is widely accepted as associated... 
Thalassemia | Genetic aspects | Research | Analysis | Genetic polymorphisms | Fetal hemoglobin
Journal Article
Experimental Biology and Medicine, ISSN 1535-3702, 11/2009, Volume 234, Issue 11, pp. 1374 - 1382
Journal Article
INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, ISSN 0971-4502, 01/2018, Volume 34, Issue 1, pp. 185 - 187
Journal Article
Annals of hematology, ISSN 0939-5555, 09/2019, pp. 1 - 9
Sickle cell anemia (SCA) is an autosomal recessive monogenic disease with significant clinical variability. Cerebrovascular disease, particularly ischemic... 
Hemoglobin | Stroke | Sickle cell anemia
Journal Article
Science translational medicine, ISSN 1946-6234, 07/2019, Volume 11, Issue 503, p. eaaw3768
Reactivation of fetal hemoglobin (HbF) is being pursued as a treatment strategy for hemoglobinopathies. Here, we evaluated the therapeutic potential of... 
MEDICINE, RESEARCH & EXPERIMENTAL | CHIMERISM | GLOBIN | HEMATOPOIETIC STEM-CELLS | FETAL-HEMOGLOBIN | DISEASE | GENE-THERAPY | SEQ | TRANSPLANTATION | CELL BIOLOGY
Journal Article