X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4052) 4052
Book Review (450) 450
Publication (221) 221
Book / eBook (16) 16
Book Chapter (15) 15
Conference Proceeding (2) 2
Magazine Article (2) 2
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (3580) 3580
humans (3497) 3497
trisomy (2586) 2586
female (2407) 2407
male (1836) 1836
adult (1140) 1140
genetics & heredity (1049) 1049
karyotyping (1017) 1017
pregnancy (830) 830
middle aged (686) 686
infant, newborn (619) 619
in situ hybridization, fluorescence (616) 616
trisomy - genetics (607) 607
chromosome aberrations (583) 583
oncology (556) 556
down syndrome (524) 524
aged (515) 515
infant (493) 493
animals (487) 487
pathology (422) 422
trisomy 21 (421) 421
phenotype (416) 416
child (396) 396
mosaicism (391) 391
mice (390) 390
child, preschool (381) 381
aneuploidy (379) 379
hematology (375) 375
abnormalities, multiple - genetics (374) 374
translocation, genetic (368) 368
down syndrome - genetics (358) 358
adolescent (357) 357
obstetrics & gynecology (356) 356
down syndrome - pathology (343) 343
chromosome disorders (335) 335
chromosomes (325) 325
abridged index medicus (321) 321
trisomy - pathology (308) 308
prenatal diagnosis (285) 285
abnormalities, multiple - pathology (279) 279
cytogenetics (272) 272
abnormalities (266) 266
analysis (247) 247
chromosome deletion (246) 246
diagnosis (242) 242
chromosomes, human, pair 18 (241) 241
chromosomes, human, pair 8 (241) 241
pediatrics (240) 240
chromosome banding (236) 236
disease models, animal (220) 220
aged, 80 and over (219) 219
prognosis (216) 216
trisomy - diagnosis (214) 214
in-situ hybridization (192) 192
cancer (191) 191
genetic aspects (190) 190
neurosciences (188) 188
syndrome (183) 183
research (180) 180
gestational age (178) 178
leukemia (176) 176
cytogenetic analysis (171) 171
bone marrow - pathology (167) 167
down's syndrome (165) 165
genes (165) 165
down-syndrome (161) 161
ultrasonography, prenatal (161) 161
cell biology (160) 160
gene (158) 158
chromosome aberrations - pathology (154) 154
translocation (153) 153
comparative genomic hybridization (152) 152
chromosomes, human, 13-15 (151) 151
fetuses (151) 151
fish (150) 150
chromosomes, human, pair 13 (149) 149
trisomy 18 (149) 149
children (148) 148
genetics (147) 147
monosomy (144) 144
retrospective studies (144) 144
expression (142) 142
tumors (142) 142
chromosome aberrations - genetics (137) 137
leukemia, lymphocytic, chronic, b-cell - genetics (137) 137
mutation (137) 137
chromosomes, human, 16-18 (135) 135
chromosomes, human, pair 7 (133) 133
prenatal-diagnosis (133) 133
gene expression (132) 132
immunohistochemistry (131) 131
article (130) 130
chromosomes, human, pair 12 (129) 129
fetus (128) 128
down syndrome - complications (122) 122
cells, cultured (121) 121
chromosomes, human, pair 18 - genetics (118) 118
risk factors (118) 118
biochemistry & molecular biology (117) 117
leukemia, myeloid, acute - genetics (117) 117
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (12) 12
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Robarts - Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
OISE - Stacks (1) 1
Providence Healthcare - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3816) 3816
French (66) 66
German (47) 47
Russian (30) 30
Japanese (25) 25
Chinese (23) 23
Spanish (22) 22
Italian (17) 17
Polish (13) 13
Czech (5) 5
Hungarian (5) 5
Korean (4) 4
Romanian (2) 2
Croatian (1) 1
Dutch (1) 1
Portuguese (1) 1
Ukrainian (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, 2010, Volume 5, Issue 5, pp. e10659 - e10659
Down syndrome (DS, trisomy 21) is the most common chromosomal disorder and the leading genetic cause of intellectual disability in humans. In DS, triplication... 
DEMENTIA | CATARACTS | DEPOSITION | MULTIDISCIPLINARY SCIENCES | HYPOTHESIS | PEOPLE | PROTEIN-PRECURSOR | CRYSTALLIN | CDNA | EXPRESSION | LOCUS | Down Syndrome - metabolism | Humans | Middle Aged | Cataract - pathology | Child, Preschool | Eye Proteins - chemistry | Molecular Sequence Data | Lens, Crystalline - ultrastructure | Male | Lens, Crystalline - pathology | Alzheimer Disease - pathology | Young Adult | Light | Amyloid beta-Peptides - metabolism | Brain - ultrastructure | Protein Structure, Quaternary | Aged, 80 and over | Adult | Female | Scattering, Radiation | Child | Amino Acid Sequence | Down Syndrome - pathology | Aging - pathology | Eye Proteins - metabolism | Adolescent | Alzheimer Disease - metabolism | Brain - pathology | Aged | Amyloid beta-Peptides - chemistry | Aging - metabolism | Cataracts | Brain | Neurosciences | Trisomy | Peptides | Laboratories | Pathogenesis | Cognitive ability | Accumulation | Medical schools | Proteins | Genotype & phenotype | Down's syndrome | Etiology | Surgery | Aging | Genetics | Alzheimer's disease | Age | Enzyme-linked immunosorbent assay | Enzymes | Phenotypes | Incubation | Neurodegenerative diseases | Complications | Light scattering | Down syndrome | Gene expression | Amyloid precursor protein | Children & youth | Pathology | Neurology | Hypotheses | Womens health | Chromosome 21 | Alzheimers disease | Protein interaction | Lenses | Dementia | Index Medicus
Journal Article
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 7/2018, Volume 55, Issue 7, pp. 5962 - 5975
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 05/2016, Volume 40, Issue 5, pp. 676 - 688
Hepatosplenic T-cell lymphoma (HSTCL) is a rare type of lymphoma. Patients have a poor prognosis, and there is no standard of care. We evaluated 28 HSTCL... 
Stem cell transplant | Hepatosplenic T-cell lymphoma | Prognostic factors | SURGERY | stem cell transplant | ENTITY | hepatosplenic T-cell lymphoma | GRANULAR LYMPHOCYTIC-LEUKEMIA | BONE-MARROW | prognostic factors | THERAPIES | PATHOLOGY | PERIPHERAL-BLOOD INVOLVEMENT | SEZARY-SYNDROME | TUMORS | Immunohistochemistry | Humans | Middle Aged | Child, Preschool | Male | Receptors, Antigen, T-Cell, alpha-beta - immunology | Receptors, Antigen, T-Cell, gamma-delta - genetics | Isochromosomes | Young Adult | Time Factors | Aged, 80 and over | Liver Neoplasms - pathology | Child | Genetic Predisposition to Disease | Liver Neoplasms - genetics | Risk Factors | Splenic Neoplasms - genetics | In Situ Hybridization, Fluorescence | Liver Neoplasms - immunology | Receptors, Antigen, T-Cell, gamma-delta - immunology | Bone Marrow Examination | Chromosomes, Human, Pair 7 | Lymphoma, T-Cell - drug therapy | Phenotype | Trisomy - genetics | Adolescent | Therapeutics | Biomarkers, Tumor - genetics | Hepatomegaly - pathology | Chromosomes, Human, Pair 8 - genetics | Lymphoma, T-Cell - immunology | Splenic Neoplasms - immunology | United States | Splenomegaly - pathology | Liver Neoplasms - mortality | Splenic Neoplasms - mortality | Adult | Female | Retrospective Studies | Splenic Neoplasms - drug therapy | Biomarkers, Tumor - analysis | Kaplan-Meier Estimate | Liver Neoplasms - drug therapy | Proportional Hazards Models | Lymphoma, T-Cell - genetics | Receptors, Antigen, T-Cell, alpha-beta - genetics | Disease-Free Survival | Splenic Neoplasms - pathology | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Bone Marrow - pathology | Lymphoma, T-Cell - pathology | Aged | Lymphoma, T-Cell - mortality | Index Medicus
Journal Article
Human Pathology, ISSN 0046-8177, 2015, Volume 50, pp. 109 - 117
Summary Hepatosplenic T-cell lymphoma (HSTCL) is a rare T-cell lymphoma commonly associated with cytopenias. The pathogenesis of cytopenias in patients with... 
Pathology | Fluorescence in situ hybridization (FISH) | Hepatosplenic T-cell lymphoma | Myelodysplasia | Pancytopenia | Trisomy 8 | ABNORMALITIES | PATHOLOGY | Splenic Neoplasms - therapy | Humans | Middle Aged | Child, Preschool | Liver Neoplasms - complications | Male | Lymphoma, T-Cell - complications | Neutropenia - etiology | Thrombocytopenia - genetics | Young Adult | Time Factors | Neutropenia - mortality | Aged, 80 and over | Liver Neoplasms - pathology | Neutropenia - blood | Child | Genetic Predisposition to Disease | Liver Neoplasms - genetics | Risk Factors | Splenic Neoplasms - genetics | In Situ Hybridization, Fluorescence | Thrombocytopenia - pathology | Bone Marrow Examination | Phenotype | Trisomy - genetics | Lymphoma, T-Cell - therapy | Adolescent | Neutropenia - therapy | Thrombocytopenia - mortality | Biomarkers, Tumor - genetics | Myelodysplastic Syndromes - pathology | Chromosomes, Human, Pair 8 - genetics | Prognosis | Liver Neoplasms - therapy | Liver Neoplasms - mortality | Splenic Neoplasms - mortality | Splenic Neoplasms - complications | Neutropenia - pathology | Adult | Female | Thrombocytopenia - therapy | Neutropenia - genetics | Thrombocytopenia - etiology | Kaplan-Meier Estimate | Lymphoma, T-Cell - genetics | Myelodysplastic Syndromes - complications | Thrombocytopenia - blood | Platelet Count | Splenic Neoplasms - pathology | Bone Marrow - pathology | Lymphoma, T-Cell - pathology | Lymphocyte Count | Aged | Myelodysplastic Syndromes - genetics | Lymphoma, T-Cell - mortality | Fluorescence | Non-Hodgkin's lymphomas | T cells | Analysis | Laboratories | Biopsy | Colleges & universities | Bone marrow | Lymphomas | Patients | Methods | Index Medicus
Journal Article
The Journal of Comparative Neurology, ISSN 0021-9967, 10/2007, Volume 504, Issue 4, pp. 329 - 345
Journal Article