X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (18392) 18392
Publication (2275) 2275
Newsletter (1103) 1103
Book Chapter (227) 227
Book Review (159) 159
Magazine Article (39) 39
Conference Proceeding (34) 34
Newspaper Article (26) 26
Government Document (25) 25
Dissertation (18) 18
Book / eBook (11) 11
Web Resource (11) 11
Reference (9) 9
Streaming Video (2) 2
Data Set (1) 1
Journal / eJournal (1) 1
Presentation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (13368) 13368
index medicus (5874) 5874
female (5019) 5019
male (4223) 4223
ataxia-telangiectasia (3733) 3733
animals (3708) 3708
ataxia telangiectasia mutated proteins (3636) 3636
dna damage (3611) 3611
ataxia telangiectasia (2953) 2953
adult (2720) 2720
middle aged (2511) 2511
cell biology (2480) 2480
oncology (2378) 2378
dna repair (2371) 2371
biochemistry & molecular biology (2370) 2370
protein-serine-threonine kinases - metabolism (2316) 2316
cancer (2272) 2272
phosphorylation (2247) 2247
cell cycle proteins - metabolism (2182) 2182
hereditary hemorrhagic telangiectasia (2160) 2160
mice (2112) 2112
mutation (1945) 1945
research (1939) 1939
dna-binding proteins - metabolism (1938) 1938
atm (1850) 1850
genetics & heredity (1816) 1816
dna (1811) 1811
protein-serine-threonine kinases - genetics (1743) 1743
ataxia telangiectasia - genetics (1741) 1741
aged (1682) 1682
genetic aspects (1548) 1548
child (1547) 1547
cell cycle proteins - genetics (1504) 1504
tumor suppressor proteins - metabolism (1459) 1459
ionizing-radiation (1454) 1454
apoptosis (1412) 1412
dna-binding proteins - genetics (1411) 1411
cell line (1392) 1392
ataxia (1391) 1391
telangiectasia, hereditary hemorrhagic - complications (1391) 1391
cell cycle (1312) 1312
double-strand breaks (1308) 1308
signal transduction (1278) 1278
dna-damage (1249) 1249
adolescent (1242) 1242
ataxia telangiectasia mutated proteins - metabolism (1131) 1131
proteins (1102) 1102
cell line, tumor (1096) 1096
article (1056) 1056
tumor suppressor proteins - genetics (1037) 1037
dna-binding proteins (1006) 1006
p53 (996) 996
tumor suppressor proteins (975) 975
tumor suppressor protein p53 - metabolism (962) 962
telangiectasia (957) 957
radiology, nuclear medicine & medical imaging (941) 941
cells, cultured (927) 927
gene (917) 917
cell cycle proteins (906) 906
repair (881) 881
telangiectasis (880) 880
ataxia telangiectasia mutated proteins - genetics (837) 837
activation (835) 835
protein (815) 815
cells (782) 782
child, preschool (782) 782
biology (770) 770
expression (761) 761
analysis (758) 758
telangiectasia, hereditary hemorrhagic - diagnosis (715) 715
mutations (714) 714
nuclear proteins - metabolism (712) 712
dna-damage response (711) 711
risk factors (687) 687
care and treatment (685) 685
telangiectasia, hereditary hemorrhagic (684) 684
deoxyribonucleic acid--dna (676) 676
genes (659) 659
histones - metabolism (646) 646
surgery (642) 642
kinases (627) 627
dna replication (626) 626
multidisciplinary sciences (625) 625
oxidative stress (624) 624
molecular sequence data (616) 616
phenotype (614) 614
telangiectasia, hereditary hemorrhagic - genetics (611) 611
gene expression (595) 595
genetic research (590) 590
health aspects (585) 585
radiation (585) 585
research article (581) 581
protein kinases - metabolism (578) 578
hela cells (574) 574
diagnosis (573) 573
breast cancer (572) 572
physiological aspects (571) 571
dna breaks, double-stranded (569) 569
homologous recombination (567) 567
saccharomyces-cerevisiae (560) 560
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (9) 9
Online Resources - Online (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Knox College (Caven) - Stacks (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (17709) 17709
French (537) 537
German (349) 349
Spanish (274) 274
Japanese (213) 213
Russian (163) 163
Italian (98) 98
Polish (90) 90
Chinese (74) 74
Korean (68) 68
Portuguese (47) 47
Dutch (35) 35
Turkish (33) 33
Danish (19) 19
Romanian (17) 17
Czech (15) 15
Hungarian (15) 15
Croatian (6) 6
Norwegian (6) 6
Slovak (6) 6
Bulgarian (4) 4
Hebrew (4) 4
Swedish (4) 4
Finnish (3) 3
Bosnian (2) 2
Greek (2) 2
Catalan (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


Clinical Genetics, ISSN 0009-9163, 2016, Volume 90, Issue 2, pp. 105 - 117
Ataxia-telangiectasia (AT) is an autosomal recessive neurodegenerative disorder with immunodeficiency and an increased risk of developing cancer, caused by... 
ataxia‐telangiectasia | heterozygote | risk factor | ATM protein | ataxia-telangiectasia | VARIANTS | FANCONI-ANEMIA | RADIATION | CARRIERS | XERODERMA-PIGMENTOSUM | BREAST-CANCER RISK | FAMILIES | GENETICS & HEREDITY | RADIOSENSITIVITY | EXPRESSION | ATM GENE-MUTATIONS | Myocardial Ischemia - genetics | Gastrointestinal Neoplasms - genetics | Humans | Middle Aged | Breast Neoplasms - etiology | Genetic Counseling | Gastrointestinal Neoplasms - pathology | Life Expectancy | Adult | Female | Ataxia Telangiectasia - complications | Myocardial Ischemia - diagnosis | Ataxia Telangiectasia - diagnosis | Gene Expression | Genetic Predisposition to Disease | Risk Factors | Gastrointestinal Neoplasms - diagnosis | Evidence-Based Medicine | Gastrointestinal Neoplasms - etiology | Myocardial Ischemia - pathology | Breast Neoplasms - genetics | Myocardial Ischemia - etiology | Breast Neoplasms - pathology | Ataxia Telangiectasia - pathology | Ataxia Telangiectasia - genetics | Heterozygote | Breast Neoplasms - diagnosis | Mutation | Ataxia Telangiectasia Mutated Proteins - genetics | Practice Guidelines as Topic | Nervous system diseases | Oncology, Experimental | Mortality | Practice guidelines (Medicine) | Ataxia | Ataxia telangiectasia | Research | Heart diseases | Health aspects | Risk factors | Cancer | Hormone replacement therapy | Breast cancer | Health risk assessment
Journal Article
Science, ISSN 0036-8075, 10/2010, Volume 330, Issue 6003, pp. 517 - 521
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 04/2017, Volume 101, Issue 4, pp. 927 - 947
Decreased ATM expression leads to accumulation of cytosolic DNA and neuroinflammation. Mutations in the ataxia‐telangiectasia (A‐T)‐mutated (ATM) gene give... 
ataxia‐telangiectasia | autoinflammatory | innate immunity | cGAS/STING | Innate immunity | Ataxia-telangiectasia | Autoinflammatory | OXIDATIVE STRESS | DEPENDENT PHOSPHORYLATION | AUTOPHOSPHORYLATION SITES | ATAXIA-TELANGIECTASIA GENE | DEFICIENT MICE | IMMUNOLOGY | CELL BIOLOGY | ataxia-telangiectasia | MUTANT MICE | NEURONAL DEATH | IN-VIVO | MOUSE MODEL | MRN COMPLEX | HEMATOLOGY | Amino Acid Sequence | Microglia - metabolism | Ataxia Telangiectasia Mutated Proteins - chemistry | Nerve Degeneration - genetics | Rats | NF-kappa B - metabolism | DNA - metabolism | DNA Repair - genetics | Longevity | Mutation, Missense - genetics | Protein Transport | Phenotype | Animals | Cell Nucleus - metabolism | Interferon-beta - metabolism | Cell Death | Brain - pathology | DNA Damage - genetics | Inflammation - genetics | Microglia - pathology | Ataxia Telangiectasia - genetics | Cytosol - metabolism | Ataxia Telangiectasia Mutated Proteins - genetics | Cerebellum | Brain | Spinal cord | Animal models | Phosphorylation | DNA damage | Proline | Amino acids | Activation | Leucine | Accumulation | Oocytes | Atrophy | Missense mutation | Neurodegeneration | Animal tissues | Ataxia | Paralysis | Damage accumulation | Deoxyribonucleic acid--DNA | Translocation | Motor neurons | Immunodeficiency | Missense mutant | Inflammation | IL-1β | Gene expression | Microglia | Life span | Ataxia telangiectasia | Ataxia telangiectasia mutated protein | Interferon | Mutation | Cytoplasm | Tumors | Cancer
Journal Article
Molecular Cell, ISSN 1097-2765, 06/2017, Volume 66, Issue 6, pp. 801 - 817
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 07/2017, Volume 12, Issue 1, pp. 126 - 7
Journal Article
Leukemia, ISSN 0887-6924, 10/2017, Volume 31, Issue 10, pp. 2048 - 2056
Recent developments in sequencing technologies led to the discovery of a novel form of genomic instability, termed chromothripsis. This catastrophic genomic... 
REARRANGEMENT | RECOMBINATION | RESPONSES | CELLS | ONCOLOGY | DNA-DAMAGE | FREQUENCY | BREAKS | MATURE | HEMATOLOGY | Genomic Instability | Humans | Neoplasm Proteins - physiology | Transcriptome | Child, Preschool | Male | DNA Repair - genetics | Telomere Shortening - genetics | Neoplasms - genetics | Female | Neoplasm Proteins - genetics | Ataxia Telangiectasia - complications | Child | In Situ Hybridization, Fluorescence | Chromosomes, Human - ultrastructure | Sequence Analysis, DNA | Ataxia Telangiectasia Mutated Proteins - physiology | Chromothripsis | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Sequence Analysis, RNA | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Adolescent | RNA, Neoplasm - genetics | Ataxia Telangiectasia - genetics | Ataxia Telangiectasia Mutated Proteins - deficiency | Neoplasm Proteins - deficiency | DNA, Neoplasm - genetics | Mutation | Ataxia Telangiectasia Mutated Proteins - genetics | Genome, Human | Precursor Cell Lymphoblastic Leukemia-Lymphoma - etiology | Usage | Gene mutations | Ataxia telangiectasia | Genetic aspects | Research | Nucleotide sequencing | Acute lymphocytic leukemia | DNA sequencing | Leukemia | DNA damage | Fluorescence | Genomes | DNA repair | Gene sequencing | Genomic instability | Fluorescence in situ hybridization | Ataxia | Tumorigenesis | Catastrophic events | Repair | Chromosomes | Deoxyribonucleic acid--DNA | Acute lymphatic leukemia | Stability | Lymphatic leukemia | Double-strand break repair | Ribonucleic acid--RNA | Patients | Telomeres | Ataxia telangiectasia mutated protein | Tumors
Journal Article
Nature Neuroscience, ISSN 1097-6256, 2013, Volume 16, Issue 12, pp. 1745 - 1753
Journal Article