X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (256) 256
index medicus (193) 193
dyskeratosis-congenita (142) 142
dyskeratosis congenita (124) 124
male (123) 123
telomerase (115) 115
mutation (93) 93
female (86) 86
hematology (85) 85
dyskeratosis congenita - genetics (81) 81
mutations (75) 75
telomeres (74) 74
adult (69) 69
aplastic-anemia (62) 62
animals (54) 54
oncology (54) 54
cancer (53) 53
bone marrow (52) 52
child (51) 51
genetic aspects (51) 51
telomerase - genetics (51) 51
telomere (51) 51
adolescent (46) 46
article (46) 46
transplantation (45) 45
research (42) 42
telomere - genetics (42) 42
middle aged (41) 41
child, preschool (39) 39
nuclear proteins - genetics (39) 39
stem cells (39) 39
dyskeratosis congenita - therapy (38) 38
pediatrics (38) 38
cell biology (37) 37
cell cycle proteins - genetics (37) 37
chromosomes (37) 37
dyskeratosis congenita - diagnosis (37) 37
disease (36) 36
dyskeratosis congenita - complications (36) 36
telomere - metabolism (35) 35
bone-marrow failure (34) 34
gene (33) 33
telomerase - metabolism (33) 33
mortality (32) 32
bone marrow failure (31) 31
dyskeratosis (31) 31
dyskeratosis congenita - pathology (31) 31
genetics & heredity (31) 31
risk factors (31) 31
aging (30) 30
hematopoietic stem cells (30) 30
pulmonary fibrosis (30) 30
diagnosis (29) 29
health aspects (29) 29
reverse-transcriptase (29) 29
aged (28) 28
proteins (28) 28
care and treatment (27) 27
mice (27) 27
telomere length (27) 27
analysis (26) 26
genetics (26) 26
biochemistry & molecular biology (25) 25
bone-marrow-transplantation (25) 25
immunology (25) 25
length (25) 25
abnormalities (24) 24
aplastic anemia (24) 24
diamond-blackfan anemia (24) 24
fanconi-anemia (24) 24
genetic predisposition to disease (24) 24
medicine (24) 24
rna (24) 24
anemia (23) 23
biology (23) 23
epithelial cells (23) 23
senescence (23) 23
abridged index medicus (22) 22
dkc1 (21) 21
hoyeraal-hreidarsson-syndrome (21) 21
leukemia (21) 21
physiological aspects (21) 21
young adult (21) 21
dna (20) 20
idiopathic pulmonary-fibrosis (20) 20
infant (20) 20
multidisciplinary sciences (20) 20
pedigree (20) 20
genes (19) 19
hematopoietic stem cell transplantation (19) 19
medicine, general & internal (19) 19
neoplasms - genetics (19) 19
pathology (19) 19
phenotype (19) 19
syndrome (19) 19
telomere - physiology (19) 19
age (18) 18
cell proliferation (18) 18
component (18) 18
genome-wide association (18) 18
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 2011, Volume 2011, pp. 480 - 486
Journal Article
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/2018, Volume 183, Issue 1, pp. 110 - 118
Journal Article
Hematology/Oncology Clinics of North America, ISSN 0889-8588, 04/2009, Volume 23, Issue 2, pp. 215 - 231
Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome characterized clinically by the triad of abnormal nails, reticular skin pigmentation,... 
Bone marrow failure | TERT | DKC1 | TERC | TINF2 | Dyskeratosis congenita | Telomere
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2011, Volume 48, Issue 5, pp. 327 - 333
Dyskeratosis congenita (DC) is a premature ageing syndrome characterised by short telomeres. An X-linked form of DC is caused by mutations in DKC1 which... 
HUMAN-DISEASE | GENE | H/ACA | CHROMOSOME INACTIVATION | GENETICS & HEREDITY | MUTATIONS | IDIOPATHIC PULMONARY-FIBROSIS | HUMAN BREAST-CANCER | IDENTIFICATION | APLASTIC-ANEMIA | RNA COMPONENT | X Chromosome Inactivation - genetics | Humans | Infant | Male | Pulmonary Fibrosis - genetics | Dyskeratosis Congenita - genetics | Dyskeratosis Congenita - mortality | RNA - genetics | Telomerase - genetics | Cell Cycle Proteins - genetics | Telomerase - metabolism | Dyskeratosis Congenita - metabolism | Pulmonary Fibrosis - metabolism | Telomere - metabolism | Genetic Linkage - genetics | Nuclear Proteins - genetics | Child | Infant, Newborn | RNA - metabolism | Telomere - genetics | Cell Cycle Proteins - metabolism | Nuclear Proteins - metabolism | Pulmonary Fibrosis - pathology | Mutation - genetics | Phenotype | Pedigree | Adolescent | Dyskeratosis Congenita - pathology | Regulatory Elements, Transcriptional - genetics | Gene mutations | Epithelial cells | Abnormalities | Physiological aspects | Genetic aspects | Research | Telomerase | Health aspects | Enzymes | Genes | Mortality | Genomes | Family medical history | Defects | Studies | Proteins | Pulmonary fibrosis | Bone marrow | Mutation | Charitable foundations | Telomere Biology | dyskeratosis congenita | genetics | dyskerin | pulmonary fibrosis | haematology (incl blood transfusion) | respiratory medicine | 1506
Journal Article
Journal Article
Journal Article
International Journal of Oral & Maxillofacial Surgery, ISSN 0901-5027, 2015, Volume 45, Issue 6, pp. 760 - 763
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2017, Volume 23, Issue 9, pp. 1422 - 1428
Abstract Patients with inherited bone marrow failure syndromes (IBMFS) such as Fanconi anemia (FA), dyskeratosis congenita (DC), and Diamond Blackfan anemia... 
Hematology, Oncology and Palliative Medicine | Late effects | Dyskeratosis congenita | Pediatric allogeneic hematopoietic cell transplant | Fanconi anemia | Diamond Blackfan anemia | Inherited bone marrow failure syndromes | LONG-TERM SURVIVORS | Pediatric allogeneic | 4 DECADES | NATIONAL-CANCER-INSTITUTE | IMMUNOLOGY | CHRONIC HEALTH CONDITIONS | BIALLELIC MUTATIONS | FANCONI-ANEMIA | TRANSPLANTATION | hematopoietic cell transplant | INSTITUTE/PEDIATRIC BLOOD | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | APLASTIC-ANEMIA | Bone Marrow Diseases - diagnosis | Humans | Anemia, Diamond-Blackfan - immunology | Hemoglobinuria, Paroxysmal - pathology | Anemia, Diamond-Blackfan - mortality | Dyskeratosis Congenita - mortality | Anemia, Aplastic - therapy | Fanconi Anemia - mortality | Transplantation, Homologous | Hemoglobinuria, Paroxysmal - immunology | Anemia, Aplastic - diagnosis | Bone Marrow Diseases - therapy | Dyskeratosis Congenita - diagnosis | Dyskeratosis Congenita - therapy | Anemia, Diamond-Blackfan - therapy | Hemoglobinuria, Paroxysmal - diagnosis | Child | Anemia, Aplastic - pathology | Hematopoietic Stem Cell Transplantation | International Cooperation | Bone Marrow Diseases - pathology | Consensus Development Conferences as Topic | Anemia, Diamond-Blackfan - diagnosis | Consensus | Fanconi Anemia - diagnosis | Bone Marrow Diseases - immunology | Survival Analysis | Fanconi Anemia - immunology | Fanconi Anemia - therapy | Hemoglobinuria, Paroxysmal - therapy | Dyskeratosis Congenita - immunology | Anemia, Aplastic - immunology | Pediatrics | Conferences, meetings and seminars | Immunodeficiency | Bone marrow | Genetic aspects | Transplantation | Medical screening | Conferences and conventions | Hematopoietic stem cells | Fanconi's anemia | Medical research | Epidemiology | Diseases | Medicine, Experimental | Children | dyskeratosis congenita | pediatric allogeneic hematopoietic cell transplant | late effects | inherited bone marrow failure syndromes
Journal Article
Journal Article