X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (17125) 17125
Book Review (2730) 2730
Publication (1725) 1725
Book Chapter (307) 307
Conference Proceeding (66) 66
Dissertation (36) 36
Magazine Article (24) 24
Book / eBook (20) 20
Web Resource (12) 12
Government Document (9) 9
Reference (3) 3
Journal / eJournal (2) 2
Streaming Video (2) 2
Data Set (1) 1
Paper (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (12886) 12886
humans (12575) 12575
male (6460) 6460
female (5053) 5053
animals (4102) 4102
mutation (3081) 3081
genetics & heredity (2786) 2786
adult (2489) 2489
mice (2296) 2296
child (2272) 2272
biochemistry & molecular biology (2046) 2046
apoptosis (1991) 1991
genetic diseases, x-linked (1864) 1864
genetic diseases, x-linked - genetics (1691) 1691
pedigree (1684) 1684
adolescent (1576) 1576
phenotype (1540) 1540
expression (1534) 1534
child, preschool (1502) 1502
gene (1501) 1501
immunology (1501) 1501
genetic aspects (1476) 1476
cell biology (1447) 1447
middle aged (1394) 1394
x-linked agammaglobulinemia (1346) 1346
infant (1342) 1342
x chromosome (1284) 1284
old medline (1276) 1276
proteins (1261) 1261
mutations (1239) 1239
research (1230) 1230
oncology (1125) 1125
severe combined immunodeficiency (1098) 1098
genetics (1051) 1051
analysis (1036) 1036
molecular sequence data (1020) 1020
genes (1013) 1013
x-linked inhibitor of apoptosis protein - metabolism (988) 988
genetic linkage (978) 978
pediatrics (975) 975
neurosciences (973) 973
x-linked adrenoleukodystrophy (973) 973
x-linked inhibitor (966) 966
abridged index medicus (965) 965
gene expression (949) 949
article (916) 916
clinical neurology (896) 896
apoptosis - drug effects (859) 859
cell line, tumor (848) 848
base sequence (834) 834
xiap (788) 788
activation (777) 777
cancer (765) 765
aged (757) 757
syndrome (754) 754
genes, x-linked (753) 753
dna mutational analysis (740) 740
disease (736) 736
protein (726) 726
signal transduction (719) 719
leukemia, hairy cell (711) 711
lymphatic diseases (697) 697
medicine, research & experimental (683) 683
family (680) 680
amino acid sequence (678) 678
research article (676) 676
x-linked (670) 670
x-linked inhibitor of apoptosis protein (643) 643
health aspects (637) 637
hematology (636) 636
endocrinology & metabolism (630) 630
diagnosis (628) 628
infant, newborn (628) 628
multidisciplinary sciences (627) 627
intellectual disability - genetics (624) 624
x-linked inhibitor of apoptosis protein - genetics (621) 621
genetic diseases, x-linked - diagnosis (614) 614
physiological aspects (594) 594
young adult (594) 594
cells (587) 587
mental retardation, x-linked - genetics (582) 582
identification (572) 572
medicine (572) 572
mutation - genetics (568) 568
pathology (566) 566
cells, cultured (565) 565
ophthalmology (557) 557
cell line (530) 530
polymerase chain reaction (517) 517
disease models, animal (511) 511
genotype (507) 507
genetic research (490) 490
gene mutations (488) 488
medicine & public health (486) 486
caspases - metabolism (480) 480
nf-kappa-b (470) 470
immunodeficiency (469) 469
care and treatment (457) 457
nuclear proteins - genetics (453) 453
chromosomes, human, x - genetics (449) 449
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (12) 12
Online Resources - Online (9) 9
Collection Dvlpm't (Acquisitions) - Vendor file (4) 4
Holland Bloorview Kids Rehabilitation - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
UTL at Downsview - May be requested (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (15906) 15906
French (372) 372
German (255) 255
Chinese (172) 172
Spanish (164) 164
Italian (142) 142
Japanese (121) 121
Russian (72) 72
Polish (50) 50
Portuguese (36) 36
Czech (33) 33
Dutch (29) 29
Korean (27) 27
Romanian (19) 19
Turkish (15) 15
Hungarian (11) 11
Swedish (7) 7
Serbian (5) 5
Danish (4) 4
Finnish (3) 3
Norwegian (3) 3
Hebrew (2) 2
Indonesian (2) 2
Bulgarian (1) 1
Lithuanian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


JAMA Ophthalmology, ISSN 2168-6165, 09/2018, Volume 136, Issue 9, pp. e182640 - e182640
Journal Article
Genetics of mental retardation, 12/2005
Mental retardation can follow any of the biological, environmental and psychological events that are capable of producing deficits in cognitive functions.... 
genetic | mental retardation | chromosomal abnormalities | X-linked
Journal
01/2014
Background: Recurrent spontaneous abortion (RSA) is one of the most common health complications with a strong genetic component. Several genetic disorders were... 
Linkage | X-linked | Recurrent spontaneous abortion
Web Resource
2017, First edition., Human diseases and conditions collection, ISBN 9781944749743, xii, 71 pages
Book
Internal Medicine Journal, ISSN 1444-0903, 09/2017, Volume 47, Issue S5, pp. 39 - 39
Journal Article
JOURNAL OF CLINICAL IMMUNOLOGY, ISSN 0271-9142, 08/2018, Volume 38, Issue 6, pp. 638 - 641
Journal Article
JOURNAL OF PEDIATRICS, ISSN 0022-3476, 05/2012, Volume 160, Issue 5, pp. 756 - 756
Journal Article
Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 2019
Background: Thrombocytopenia is a serious issue for all patients with classical Wiskott-Aldrich syndrome (WAS) and X-linked thrombocytopenia (XLT) because it... 
Wiskott-Aldrich syndrome | X-linked thrombocytopenia | gene therapy | platelets
Journal Article
12/2010
We herein report the joint occurrence of an autistic disorder (AD) and X-linked hypophosphatemia. X-linked hypophosphatemia (XLH), an X-linked dominant... 
genetics | Autistic disorder | X-linked hypophosphatemia | Syndromal autism spectrum disorders
Web Resource
Nature Reviews Cancer, ISSN 1474-175X, 08/2010, Volume 10, Issue 8, pp. 561 - 574
The realization that alterations in inhibitor of apoptosis (IAP) proteins are found in many types of human cancer and are associated with chemoresistance,... 
INDUCED CELL-DEATH | TUMOR-NECROSIS-FACTOR | X-LINKED INHIBITOR | ONCOLOGY | STRUCTURAL BASIS | UBIQUITIN-PROTEIN LIGASE | PANCREATIC-CANCER | ALPHA-DEPENDENT APOPTOSIS | DOWN-REGULATION | TNF-ALPHA | COMPARATIVE GENOMIC HYBRIDIZATION
Journal Article
CLINICAL CANCER RESEARCH, ISSN 1078-0432, 06/2012, Volume 18, Issue 11, pp. 3163 - 3169
Purpose: Bcl-2 is a critical regulator of apoptosis that is overexpressed in the majority of small cell lung cancers (SCLC). Nativoclax (ABT-263) is a potent... 
CARCINOMA-CELLS | CIRCULATING TUMOR-CELLS | X-LINKED INHIBITOR | PROGNOSTIC-FACTORS | SOLID TUMORS | ONCOLOGY | BCL-2 FAMILY INHIBITOR | CLINICAL-EFFICACY | GENE-EXPRESSION | APOPTOSIS PROTEIN XIAP | SMALL-MOLECULE INHIBITOR
Journal Article
Metabolism: clinical and experimental, ISSN 0026-0495, 03/2019
Early diagnosis, optimal therapeutic management and regular follow up of children with X-linked hypophosphatemia (XLH) determine their long term outcomes and... 
Journal Article
Survey of Ophthalmology, ISSN 0039-6257, 2019
A 45-year-old white woman presented with chronic bilateral, painless, progressive, peripheral vision loss. She was found to have bilateral optic atrophy and... 
optic neuropathy | X-linked | Carrier | adrenoleukodystrophy | multiple sclerosis
Journal Article
Reproductive BioMedicine Online, ISSN 1472-6483, 04/2019, Volume 38, pp. e52 - e53
Journal Article
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, ISSN 0884-0431, 10/2017, Volume 32, Issue 10, pp. 2062 - 2073
Fibroblast growth factor 23 (FGF23) is the causative factor of X-linked hypophosphatemia (XLH), a genetic disorder effecting 1:20,000 that is characterized by... 
1,25D | osteomalacia | fibroblast growth factor 23 | X-linked hypophosphatemia | phosphate
Journal Article
Pediatric Neurology, ISSN 0887-8994, 06/2019
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.