X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (7093) 7093
Newsletter (1659) 1659
Publication (1043) 1043
Newspaper Article (113) 113
Book Chapter (91) 91
Book Review (62) 62
Dissertation (36) 36
Conference Proceeding (14) 14
Magazine Article (14) 14
Book / eBook (9) 9
Web Resource (7) 7
Reference (3) 3
Government Document (2) 2
Transcript (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (5045) 5045
fanconi's anemia (3383) 3383
index medicus (2641) 2641
female (2008) 2008
research (1828) 1828
fanconi anemia - genetics (1660) 1660
cancer (1659) 1659
male (1609) 1609
fanconi anemia (1535) 1535
dna repair (1448) 1448
genetic aspects (1328) 1328
fanconi-anemia (1327) 1327
animals (1265) 1265
oncology (1147) 1147
dna damage (1098) 1098
child (1080) 1080
mutation (1037) 1037
genetics & heredity (1011) 1011
hematology (1006) 1006
dna (993) 993
adult (955) 955
biochemistry & molecular biology (946) 946
cell biology (877) 877
child, preschool (727) 727
anemia (700) 700
proteins (697) 697
adolescent (692) 692
article (657) 657
homologous recombination (654) 654
reports (647) 647
genetic research (635) 635
mice (630) 630
genes (556) 556
fanconi anemia - metabolism (551) 551
transplantation (534) 534
analysis (516) 516
cell line (507) 507
fanconi anemia - pathology (503) 503
fanconi anemia - complications (501) 501
fanconi anemia - therapy (497) 497
breast cancer (476) 476
middle aged (473) 473
care and treatment (468) 468
health aspects (459) 459
repair (451) 451
fanconi syndrome (440) 440
medical research (426) 426
hematopoietic stem cells (423) 423
infant (416) 416
pediatrics (411) 411
protein (402) 402
risk factors (396) 396
stem cells (392) 392
genetic predisposition to disease (390) 390
hemic and lymphatic diseases (387) 387
universities and colleges (384) 384
gene (383) 383
oncology, experimental (377) 377
deoxyribonucleic acid--dna (372) 372
cells, cultured (370) 370
medicine, experimental (368) 368
cells (366) 366
breast neoplasms - genetics (365) 365
nuclear proteins - genetics (365) 365
dna-binding proteins - genetics (364) 364
pathway (361) 361
fanconi anemia - diagnosis (348) 348
dna replication (347) 347
chromosome aberrations (346) 346
mutations (340) 340
bone marrow (339) 339
genomic instability (337) 337
dna-binding proteins - metabolism (326) 326
fanconi-anemia pathway (323) 323
brca2 (322) 322
cell line, tumor (321) 321
fanconi anemia complementation group proteins (321) 321
fanconi anemia complementation group proteins - genetics (319) 319
fanconi anemia complementation group d2 protein - metabolism (318) 318
fanconi anemia complementation group proteins - metabolism (318) 318
genetics (315) 315
diagnosis (313) 313
double-strand breaks (308) 308
physiological aspects (304) 304
leukemia (302) 302
molecular sequence data (297) 297
apoptosis (295) 295
phenotype (291) 291
protein binding (287) 287
cross-link repair (281) 281
aged (280) 280
brca1 (280) 280
dna-repair (278) 278
genomics (268) 268
cell cycle (267) 267
gene mutations (259) 259
gene expression (255) 255
risk (251) 251
medicine, research & experimental (250) 250
toxicology (250) 250
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (8531) 8531
French (90) 90
Spanish (63) 63
Japanese (61) 61
German (60) 60
Chinese (34) 34
Italian (24) 24
Polish (23) 23
Russian (23) 23
Portuguese (19) 19
Czech (12) 12
Croatian (8) 8
Turkish (8) 8
Dutch (5) 5
Hungarian (5) 5
Romanian (5) 5
Hebrew (4) 4
Korean (4) 4
Slovak (4) 4
Persian (3) 3
Catalan (2) 2
Serbian (2) 2
Swedish (2) 2
Danish (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2280 - 14
Defects in DNA repair can cause various genetic diseases with severe pathological phenotypes. Fanconi anemia ( FA) is a rare disease characterized by bone... 
UBIQUITINATION | DAMAGE RESPONSE | CHROMATIN | CROSS-LINK REPAIR | HUMAN-CELLS | MULTIDISCIPLINARY SCIENCES | SENSITIVITY | HOMOLOGOUS RECOMBINATION | BRCA1 | ENRICHMENT ANALYSIS | ASSOCIATION | Genetic Therapy | Ubiquitin-Specific Proteases - genetics | Fanconi Anemia Complementation Group D2 Protein - genetics | Fanconi Anemia - metabolism | Humans | DNA Repair - physiology | DNA Repair - genetics | Fanconi Anemia Complementation Group C Protein - genetics | Fanconi Anemia Complementation Group A Protein - genetics | Fanconi Anemia Complementation Group D2 Protein - deficiency | Fanconi Anemia Complementation Group A Protein - metabolism | Fanconi Anemia Complementation Group Proteins - metabolism | Ubiquitination | Fanconi Anemia Complementation Group G Protein - genetics | Ubiquitin-Specific Proteases - deficiency | Fanconi Anemia Complementation Group G Protein - deficiency | BRCA1 Protein - metabolism | Fanconi Anemia - genetics | Ubiquitin-Specific Proteases - metabolism | Chromosomal Instability | Rad51 Recombinase - metabolism | Cell Line | Fanconi Anemia Complementation Group Proteins - deficiency | Fanconi Anemia Complementation Group Proteins - genetics | Fanconi Anemia Complementation Group G Protein - metabolism | Gene Knockout Techniques | Fanconi Anemia Complementation Group C Protein - metabolism | Fanconi Anemia Complementation Group D2 Protein - metabolism | Fanconi Anemia Complementation Group A Protein - deficiency | CRISPR-Cas Systems | Fanconi Anemia Complementation Group C Protein - deficiency | Fanconi Anemia - therapy | DNA Damage | Histones - metabolism | Mutation
Journal Article
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 2011, Volume 2011, Issue 1, pp. 492 - 497
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 | NATIONAL-CANCER-INSTITUTE | SEVERE APLASTIC-ANEMIA | IMMUNOLOGY | CHRONIC HEALTH CONDITIONS | BIALLELIC MUTATIONS | FANCONI-ANEMIA | TRANSPLANTATION | hematopoietic cell transplant | CHILDHOOD-CANCER | INSTITUTE/PEDIATRIC BLOOD | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | 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
Molecular Cell, ISSN 1097-2765, 01/2017, Volume 65, Issue 2, pp. 247 - 259
Monoubiquitination and deubiquitination of FANCD2:FANCI heterodimer is central to DNA repair in a pathway that is defective in the cancer predisposition... 
core complex | RING E3 | Fanconi anemia | FANCD2 | deubiquitination | FANCB | enzyme mechanism | monoubiquitination | DNA repair | NUCLEAR ACCUMULATION | MONOUBIQUITINATED FANCD2 | TARGETED DISRUPTION | COMPLEX | DNA-REPAIR PATHWAY | CROSS-LINK REPAIR | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEINS | DAMAGE | COMPLEMENTATION GROUP-B | LIGASE | CELL BIOLOGY | Fanconi Anemia Complementation Group D2 Protein - genetics | Fanconi Anemia - metabolism | Humans | Multiprotein Complexes | Protein Multimerization | Substrate Specificity | Fanconi Anemia Complementation Group A Protein - metabolism | DNA-Binding Proteins - metabolism | Fanconi Anemia Complementation Group Proteins - metabolism | Ubiquitination | Transfection | Time Factors | Fanconi Anemia - genetics | Ubiquitin-Specific Proteases - metabolism | Recombinant Proteins - metabolism | Cell Line | Fanconi Anemia Complementation Group Proteins - genetics | Nuclear Proteins - metabolism | Fanconi Anemia Complementation Group G Protein - metabolism | DNA - metabolism | Inhibitor of Differentiation Protein 2 - metabolism | DNA - genetics | Fanconi Anemia Complementation Group C Protein - metabolism | Fanconi Anemia Complementation Group D2 Protein - metabolism | Protein Binding | Fanconi Anemia Complementation Group L Protein - metabolism | Fanconi Anemia Complementation Group E Protein - metabolism | Ubiquitin | Chemotherapy | Ligases | Genomics | Research institutes | Cancer | Fanconi's anemia | Proteins | Medical research | Molecular genetics | Medicine, Experimental
Journal Article
British Journal of Haematology, ISSN 0007-1048, 05/2017, Volume 177, Issue 4, pp. 526 - 542
The inherited bone marrow failure syndromes ( IBMFS ) typically present with significant cytopenias in at least one haematopoietic cell lineage that may... 
Fanconi anaemia | Shwachman Diamond syndrome | dyskeratosis congenita | Diamond Blackfan anaemia | inherited bone marrow failure | HOYERAAL-HREIDARSSON-SYNDROME | ACUTE MYELOGENOUS LEUKEMIA | SOMATIC MOSAICISM | FANCONI-ANEMIA | C-MPL MUTATIONS | CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA | CROSS-LINK REPAIR | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | APLASTIC-ANEMIA | Exocrine Pancreatic Insufficiency - genetics | Bone Marrow Diseases - diagnosis | Humans | Exocrine Pancreatic Insufficiency - diagnosis | Dyskeratosis Congenita - genetics | Genetic Counseling | Neutropenia - congenital | Anemia, Aplastic - diagnosis | Neutropenia - diagnosis | Dyskeratosis Congenita - diagnosis | Fanconi Anemia - genetics | Genomics - methods | Hemoglobinuria, Paroxysmal - diagnosis | Neutropenia - genetics | Anemia, Aplastic - genetics | Telomere - genetics | Blood Platelet Disorders - genetics | Hemoglobinuria, Paroxysmal - genetics | Lipomatosis - genetics | Blood Platelet Disorders - diagnosis | Anemia, Diamond-Blackfan - diagnosis | Bone Marrow Diseases - genetics | Fanconi Anemia - diagnosis | Ribosomes - genetics | Anemia, Diamond-Blackfan - genetics | Lipomatosis - diagnosis | DNA Repair-Deficiency Disorders - genetics | Genetic research | Genomics | Fanconi's anemia | Dyskeratosis | Anemia | Diamonds | Disorders | Health risks | Cell lineage | Biology | Patients | Genetic screening | Gene sequencing | Pancytopenia | Bone marrow | Diagnostic systems | Genetic counselling | Cancer
Journal Article
Journal Article
2007, Monographs in human genetics, ISBN 9783805582773, Volume 15
Web Resource
2006, Medical intelligence unit (Unnumbered), ISBN 9780387319728, 121
Aims to give research students a platform for further investigation and act as a source of information regarding experimental design. This work contains... 
Fanconi Anemia | Genetic aspects | genetics | Molecular aspects | Fanconi's anemia | Medicine | Human Genetics | Molecular Medicine | Biomedicine | Immunology
Book