X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5527) 5527
Newspaper Article (704) 704
Newsletter (129) 129
Book Chapter (45) 45
Magazine Article (15) 15
Web Resource (11) 11
Dissertation (6) 6
Publication (4) 4
Trade Publication Article (3) 3
Book / eBook (1) 1
Conference Proceeding (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
neutropenia (4063) 4063
humans (4021) 4021
female (2333) 2333
male (2307) 2307
oncology (1638) 1638
hematology (1564) 1564
chemotherapy (1455) 1455
adult (1416) 1416
middle aged (1312) 1312
patients (1175) 1175
cancer (1135) 1135
aged (1073) 1073
mutation (989) 989
neutropenia - genetics (815) 815
child (761) 761
infections (738) 738
research (732) 732
animals (730) 730
leukemia (709) 709
neutropenia - chemically induced (701) 701
pediatrics (689) 689
adolescent (668) 668
care and treatment (611) 611
immunology (611) 611
treatment outcome (611) 611
cancer therapies (594) 594
clinical trials (593) 593
child, preschool (586) 586
toxicity (581) 581
neutrophils (571) 571
genetic aspects (555) 555
infant (545) 545
health aspects (538) 538
analysis (535) 535
anemia (503) 503
medicine (496) 496
bone marrow (492) 492
risk factors (477) 477
drug dosages (462) 462
infectious diseases (456) 456
severe congenital neutropenia (455) 455
mice (451) 451
colony-stimulating factor (447) 447
research article (446) 446
pharmacology & pharmacy (433) 433
medical research (428) 428
neutropenia - congenital (416) 416
children (406) 406
medicine & public health (401) 401
stem cells (401) 401
antineoplastic combined chemotherapy protocols - therapeutic use (390) 390
lymphomas (390) 390
blood (388) 388
survival (386) 386
neutropenia - complications (383) 383
antineoplastic combined chemotherapy protocols - adverse effects (380) 380
drug therapy (378) 378
multidisciplinary sciences (377) 377
aged, 80 and over (375) 375
therapy (373) 373
young adult (370) 370
diagnosis (365) 365
disease (364) 364
metastasis (364) 364
mortality (364) 364
genotype (350) 350
retrospective studies (350) 350
mutations (342) 342
studies (329) 329
gene (328) 328
science (323) 323
tumors (317) 317
proteins (308) 308
transplantation (302) 302
expression (301) 301
neutropenia - etiology (299) 299
prognosis (299) 299
genetics & heredity (289) 289
thrombocytopenia (285) 285
diarrhea (281) 281
fever (277) 277
febrile neutropenia (276) 276
abridged index medicus (272) 272
breast cancer (271) 271
apoptosis (265) 265
leukocytes (265) 265
medicine, experimental (265) 265
phenotype (262) 262
infection (258) 258
medical prognosis (255) 255
pharmacokinetics (255) 255
laboratories (254) 254
microbiology (251) 251
fda approval (250) 250
granulocyte colony-stimulating factor - therapeutic use (250) 250
granulocyte colony-stimulating factor (249) 249
antibiotics (247) 247
syndrome (245) 245
genetic disorders (243) 243
neutropenia - immunology (242) 242
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6309) 6309
Japanese (45) 45
French (28) 28
Chinese (24) 24
German (17) 17
Spanish (17) 17
Russian (11) 11
Polish (7) 7
Turkish (5) 5
Hungarian (4) 4
Swedish (4) 4
Korean (3) 3
Hebrew (2) 2
Italian (2) 2
Afrikaans (1) 1
Croatian (1) 1
Danish (1) 1
Dutch (1) 1
Portuguese (1) 1
Romanian (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9258
Background: The Notch pathway is essential for proper epidermal differentiation during embryonic skin development. Moreover, skin specific loss of Notch... 
HUMAN EPITHELIAL-CELLS | IN-VITRO | MOUSE KERATINOCYTES | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | GROWTH | IGM(+) B-CELLS | MICE | T-CELL | EXPRESSION | THYMIC STROMAL LYMPHOPOIETIN | Dermatitis, Atopic - genetics | Skin - metabolism | Humans | Receptor, Notch2 - genetics | Receptors, Notch - genetics | Myeloproliferative Disorders - genetics | Granulocyte Colony-Stimulating Factor - genetics | Dermatitis, Atopic - mortality | Flow Cytometry | Receptors, Cytokine - metabolism | Receptors, Cytokine - genetics | Granulocyte Colony-Stimulating Factor - metabolism | Skin - pathology | Immunoglobulins | Cytokines - metabolism | Mice, Inbred C57BL | Receptors, Notch - physiology | Mice, Transgenic | Survival Rate | Signal Transduction - genetics | Dermatitis, Atopic - physiopathology | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Receptor, Notch2 - physiology | Animals | Mice, Nude | Models, Biological | Survival Analysis | Myeloproliferative Disorders - physiopathology | Signal Transduction - physiology | Mice | Skin - physiopathology | Receptor, Notch1 - genetics | Myeloproliferative Disorders - mortality | Receptor, Notch1 - physiology | Embryonic development | Psoriasis | Atopic dermatitis | Bone marrow | Transplantation | Skin | B cells | Syngeneic grafts | Pathogenesis | Bone marrow transplantation | Homeostasis | Lichen planus | Inactivation | Dermatitis | Thymus | Signal transduction | Embryogenesis | Biomedical materials | Immunology | Granulocytes | Granulocyte colony-stimulating factor | Lymphocytes | Rodents | Biocompatibility | Drug dosages | Osteopenia | Neutropenia | Spleen | Repressing | Deactivation | Cytokines | Developmental biology | Dermatology | Leukocytes (eosinophilic) | Neutrophils | Keratinocytes | Breast cancer | Gene expression | Myeloproliferative diseases | Hemopoiesis | Signaling | Thymic stromal lymphopoietin | Stem cells | Mast cells | Infiltration | Notch protein | Hematopoietic system | Mutation | Eosinophils
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2015, Volume 96, Issue 2, pp. 258 - 265
Journal Article
American journal of human genetics, ISSN 0002-9297, 2015, Volume 96, Issue 2, pp. 245 - 257
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2016, Volume 99, Issue 1, pp. 174 - 187
Journal Article
PLoS genetics, ISSN 1553-7404, 2009, Volume 5, Issue 1, p. e1000360
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2014, Volume 9, Issue 1, p. e85362
Systemic mastocytosis with associated hematologic clonal non-mast cell disease (SM-AHNMD) is a rare and heterogeneous subtype of SM and few studies on this... 
CRITERIA | KITD816V | POLYCYTHEMIA-VERA | LINEAGE DISEASES | MULTIDISCIPLINARY SCIENCES | Prognosis | Cell Count | Hematologic Neoplasms - mortality | Humans | Middle Aged | Male | Mastocytosis, Systemic - diagnosis | Mastocytosis, Systemic - genetics | Neutropenia - complications | Neutropenia - diagnosis | Monocytes - pathology | Neutropenia - mortality | Aged, 80 and over | Adult | Female | Proto-Oncogene Proteins c-kit - genetics | Hematologic Neoplasms - complications | Neutropenia - genetics | Proto-Oncogene Proteins c-cbl - genetics | Hematologic Neoplasms - diagnosis | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | DNA-Binding Proteins - genetics | Mastocytosis, Systemic - mortality | Adolescent | Survival Analysis | Aged | Hematologic Neoplasms - genetics | Mutation | Mastocytosis, Systemic - complications | Medical research | Mast cell disease | Analysis | Patient outcomes | Medicine, Experimental | Hemoglobin | Bones | Genetic aspects | Density | Splenomegaly | Mastocytosis | Disease | Laboratories | Liver | Leukemia | Multivariate analysis | Defects | Variables | Chronic myelomonocytic leukemia | Lesions | Neutropenia | Enlargement | Cell survival | Hematology | Patients | Survival | Studies | Monocytes | Medical prognosis | Tryptase | Bone mineral density | Blood diseases | Ascites | Tumors
Journal Article
PLoS computational biology, ISSN 1553-7358, 2019, Volume 15, Issue 1, p. e1006664
Cancer development is driven by series of events involving mutations, which may become fixed in a tumor via genetic drift and selection... 
COLONY-STIMULATING-FACTOR | FACTOR-RECEPTOR | PASSENGER MUTATIONS | EVOLUTION | SEVERE CONGENITAL NEUTROPENIA | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | SENSITIVITY | ACUTE MYELOID-LEUKEMIA | G-CSF | CANCER | SOMATIC MUTATIONS | Cell Cycle - genetics | Congenital Bone Marrow Failure Syndromes | Humans | Computational Biology | Leukocyte Elastase - genetics | Mutation Rate | Mutation - genetics | Myelodysplastic Syndromes - etiology | Neutropenia - congenital | Selection, Genetic - genetics | Neutropenia - complications | Receptors, Colony-Stimulating Factor - genetics | Hematologic Neoplasms - genetics | Models, Genetic | Myelodysplastic Syndromes - genetics | Neutropenia - genetics | Neutropenia - physiopathology | Epigenetic inheritance | Care and treatment | Genetic aspects | Gene mutations | Health aspects | Neutropenia | Pediatrics | Leukemia | Positive selection | Biology | Mutation rates | Malignancy | Population genetics | Myelodysplastic syndrome | Engineering | Granulocytes | Granulocyte colony-stimulating factor | Bone marrow | Genetics | Colony-stimulating factor | Mathematical models | Genetic drift | Sequences | Congenital diseases | Hematology | Myeloid leukemia | Fetuses | Neutrophils | Preventive medicine | Two phase | Progenitor cells | Hemopoiesis | Mutants | Applied mathematics | Stem cells | Drift | Mutation | Leukocytes (granulocytic) | Acute myeloid leukemia | Age composition | Cancer
Journal Article
Leukemia & lymphoma, ISSN 1029-2403, 2015, Volume 57, Issue 3, pp. 520 - 536
...). With the growing availability of clinical genetic testing, there is an increasing appreciation that a number of genetic predisposition syndromes may underlie apparent de novo presentations of MDS/AML... 
bone marrow failure | clonal hematopoiesis | genetic predisposition | aplastic anemia | familial MDS/AML | Genetic predisposition | Bone marrow failure | Aplastic anemia | Clonal hematopoiesis | Familial MDS/AML | FAMILIAL PLATELET DISORDER | PRIMARY LYMPHEDEMA | SEVERE CONGENITAL NEUTROPENIA | SHWACHMAN-DIAMOND SYNDROME | FANCONI-ANEMIA | ACQUIRED APLASTIC-ANEMIA | ONCOLOGY | AUTOSOMAL-DOMINANT | STEM-CELL TRANSPLANTATION | HEMATOLOGY | BONE-MARROW FAILURE | Age Factors | Humans | Leukemia, Myeloid, Acute - epidemiology | Signal Recognition Particle - genetics | Male | Genetic Counseling | Incidence | Myelodysplastic Syndromes - prevention & control | Thrombocytopenia - genetics | Female | CCAAT-Enhancer-Binding Proteins - genetics | Genomics - methods | Nuclear Proteins - genetics | GATA2 Transcription Factor - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Leukemia, Myeloid, Acute - prevention & control | Myelodysplastic Syndromes - epidemiology | Syndrome | Haploinsufficiency | DEAD-box RNA Helicases - genetics | Myelodysplastic Syndromes - diagnosis | Leukemia, Myeloid, Acute - diagnosis | Thrombocytopenia - diagnosis | Disease Management | Myelodysplastic Syndromes - genetics | Core Binding Factor Alpha 2 Subunit - genetics | Population Surveillance | Leukemia, Myeloid, Acute - genetics | familial MDS | AML
Journal Article
Blood, ISSN 1528-0020, 2013, Volume 121, Issue 5, pp. 822 - 829
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 1/2017, Volume 40, Issue 1, pp. 121 - 130
Journal Article