X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (55561) 55561
Book Review (6125) 6125
Publication (4128) 4128
Conference Proceeding (1340) 1340
Book Chapter (1277) 1277
Patent (731) 731
Dissertation (493) 493
Magazine Article (149) 149
Book / eBook (126) 126
Paper (38) 38
Report (27) 27
Government Document (24) 24
Web Resource (19) 19
Reference (9) 9
Data Set (7) 7
Trade Publication Article (7) 7
Journal / eJournal (5) 5
Newsletter (4) 4
Newspaper Article (4) 4
Microfilm (2) 2
Streaming Video (1) 1
Technical Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (36978) 36978
humans (27994) 27994
female (17426) 17426
genes, dominant (16996) 16996
male (16761) 16761
animals (12552) 12552
adult (9427) 9427
mutation (9292) 9292
pedigree (7772) 7772
middle aged (6938) 6938
genetics & heredity (6661) 6661
mice (5713) 5713
phenotype (5230) 5230
biochemistry & molecular biology (4954) 4954
child (4420) 4420
adolescent (4159) 4159
aged (3769) 3769
genetic aspects (3621) 3621
gene (3463) 3463
analysis (3452) 3452
molecular sequence data (3416) 3416
research (3393) 3393
genetics (3143) 3143
clinical neurology (3090) 3090
cell biology (2949) 2949
abridged index medicus (2935) 2935
neurosciences (2906) 2906
genes (2870) 2870
mutations (2656) 2656
child, preschool (2604) 2604
base sequence (2566) 2566
expression (2554) 2554
alleles (2474) 2474
genotype (2416) 2416
genetic linkage (2376) 2376
genes, dominant - genetics (2325) 2325
dominant species (2308) 2308
genes, recessive (2301) 2301
amino acid sequence (2272) 2272
chromosome mapping (2253) 2253
proteins (2219) 2219
studies (2175) 2175
dna mutational analysis (1967) 1967
urology & nephrology (1916) 1916
syndrome (1910) 1910
dominant (1884) 1884
disease (1758) 1758
infant (1724) 1724
cell line (1713) 1713
mutation - genetics (1686) 1686
article (1654) 1654
gene expression (1643) 1643
research article (1616) 1616
heterozygote (1587) 1587
management (1570) 1570
transfection (1570) 1570
protein (1563) 1563
ophthalmology (1556) 1556
signal transduction (1553) 1553
multidisciplinary sciences (1522) 1522
rats (1521) 1521
identification (1502) 1502
time factors (1485) 1485
family (1470) 1470
physiological aspects (1407) 1407
polymerase chain reaction (1391) 1391
autosomal dominant (1365) 1365
cells, cultured (1338) 1338
risk factors (1312) 1312
apoptosis (1260) 1260
pregnancy (1256) 1256
polycystic kidney, autosomal dominant - genetics (1248) 1248
models, genetic (1243) 1243
infant, newborn (1237) 1237
gene mutations (1233) 1233
life sciences (1233) 1233
endocrinology & metabolism (1226) 1226
medicine (1205) 1205
ecology (1164) 1164
diagnosis (1159) 1159
genetic markers (1159) 1159
business (1154) 1154
cells (1142) 1142
young adult (1120) 1120
genetic predisposition to disease (1106) 1106
phosphorylation (1102) 1102
oncology (1094) 1094
protein binding (1089) 1089
magnetic resonance imaging (1085) 1085
dna (1083) 1083
biology (1074) 1074
autosomal dominant polycystic kidney disease (1063) 1063
medicine, research & experimental (1061) 1061
genetic research (1049) 1049
disease models, animal (1038) 1038
dominant logic (1038) 1038
models, biological (1026) 1026
chromosome disorders (1017) 1017
autosomal-dominant (1011) 1011
diagnosis, differential (996) 996
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (24) 24
UTL at Downsview - May be requested (10) 10
UofT at Mississauga - Stacks (8) 8
Online Resources - Online (7) 7
Gerstein Science - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
St. Michael's College (John M. Kelly) - 3rd Floor (3) 3
Media Commons - Microtexts (2) 2
New College (Ivey) - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
UofT at Scarborough - Withdrawn (2) 2
Art - Library use only (1) 1
Criminology - Stacks (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Law (Bora Laskin) - Stacks (1) 1
OISE - Stacks (1) 1
OISE - Theses (1) 1
Robarts - Government Pubs (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
University Archives - Archives (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (52798) 52798
French (1638) 1638
German (775) 775
Swedish (748) 748
Spanish (573) 573
Japanese (565) 565
Russian (507) 507
Korean (429) 429
Chinese (406) 406
Portuguese (171) 171
Italian (111) 111
Polish (99) 99
Czech (64) 64
Dutch (64) 64
Hungarian (37) 37
Persian (33) 33
Turkish (32) 32
Croatian (20) 20
Finnish (20) 20
Romanian (16) 16
Danish (15) 15
Indonesian (15) 15
Vietnamese (15) 15
Lithuanian (13) 13
Catalan (11) 11
Slovak (10) 10
Bulgarian (9) 9
Norwegian (9) 9
Afrikaans (8) 8
Greek (7) 7
Hebrew (4) 4
Serbian (4) 4
Slovenian (4) 4
Latin (3) 3
Malay (3) 3
Arabic (2) 2
Ukrainian (2) 2
Estonian (1) 1
Macedonian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2015, Sixth edition., ISBN 1608311767, xii, 576 pages
Top experts from all over the world have been brought together by the editors, to give a world of expertise on this important subject, with a strong emphasis... 
Parkinson Disease | Movement Disorders
Book
Cardiovascular Research, ISSN 0008-6363, 06/2012, Volume 94, Issue 3, pp. 408 - 417
Journal Article
Brain, ISSN 0006-8950, 03/2010, Volume 133, Issue 3, pp. 771 - 786
Journal Article
Brain, ISSN 0006-8950, 2/2008, Volume 131, Issue 2, pp. 329 - 337
Journal Article
Brain, ISSN 0006-8950, 2/2008, Volume 131, Issue 2, pp. 338 - 351
Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organization and control of apoptosis, have been linked to non-syndromic... 
Chronic progressive external ophthalmoplegia | Dominant optic atrophy | Mitochondrial encephalomyopathy | Mitochondria | mtDNA multiple deletions | PROTEIN | mitochondria | NEUROSCIENCES | chronic progressive external ophthalmoplegia | R445H MUTATION | CLINICAL NEUROLOGY | mitochondrial encephalomyopathy | PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY | HEARING-LOSS | GENE | DISEASE | dominant optic atrophy | DEAFNESS | FISSION | DELETIONS | Ophthalmoplegia, Chronic Progressive External - pathology | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Mutation, Missense | DNA Mutational Analysis - methods | Ophthalmoplegia, Chronic Progressive External - genetics | DNA, Mitochondrial - genetics | Base Sequence | Muscle, Skeletal - chemistry | Adult | Female | Optic Atrophy, Autosomal Dominant - pathology | Child | Muscle, Skeletal - ultrastructure | Models, Molecular | Fibroblasts - pathology | Mitochondrial Myopathies - pathology | Syndrome | Magnetic Resonance Imaging | Point Mutation | Mitochondrial Myopathies - genetics | GTP Phosphohydrolases - genetics | Pedigree | Optic Atrophy, Autosomal Dominant - genetics | Aged | Index Medicus | Abridged Index Medicus | GTP Phosphohydrolases | Neurons and Cognition | DNA, Mitochondrial | Life Sciences | DNA Mutational Analysis | Fibroblasts | Optic Atrophy, Autosomal Dominant | Mitochondrial Myopathies | Ophthalmoplegia, Chronic Progressive External | Muscle, Skeletal
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 1931-857X, 05/2011, Volume 300, Issue 5, pp. 1193 - 1202
Autosomal dominant polycystic kidney disease (ADPKD) caused by mutations in either the PKD1 or PKD2 gene is a major cause of end-stage renal failure. A number... 
Multitarget therapy | Autosomal dominant polycystic kidney disease | Signal transducers and activator of transcription 3 | Mammalian target of rapamycin | CANCER-CELLS | MAMMALIAN TARGET | PHYSIOLOGY | TRITERPENOIDS | POLYCYSTIC KIDNEY-DISEASE | PANCREATIC-CANCER | PLANAR CELL POLARITY | signal transducers and activator of transcription 3 | autosomal dominant polycystic kidney disease | BETA-CATENIN | mammalian target of rapamycin | CYST FORMATION | PROSTATE-CANCER | UROLOGY & NEPHROLOGY | AUTOSOMAL-DOMINANT | multitarget therapy | Renal Insufficiency - enzymology | Phosphorylation | Kidney - pathology | TOR Serine-Threonine Kinases - metabolism | Kidney - enzymology | Polycystic Kidney, Autosomal Dominant - pathology | Renal Insufficiency - prevention & control | Dose-Response Relationship, Drug | Polycystic Kidney, Autosomal Dominant - genetics | Polycystic Kidney, Autosomal Dominant - enzymology | STAT3 Transcription Factor - metabolism | Cytoprotection | Disease Models, Animal | Renal Insufficiency - genetics | Kidney - drug effects | Cells, Cultured | Curcumin - pharmacology | Polycystic Kidney, Autosomal Dominant - prevention & control | TRPP Cation Channels - deficiency | TRPP Cation Channels - genetics | Mice, Knockout | Organ Size - drug effects | Animals | Signal Transduction - drug effects | Renal Insufficiency - pathology | Ribosomal Protein S6 - metabolism | Cell Proliferation - drug effects | Mice | Turmeric | Care and treatment | Gene mutations | Cellular signal transduction | Genetic aspects | Research | Health aspects | Risk factors | Polycystic kidney disease | Signal transduction | Kidney diseases | Cysts | Correlation analysis | Rodents | Index Medicus
Journal Article
Kidney International, ISSN 0085-2538, 10/2015, Volume 88, Issue 4, pp. 676 - 683
Journal Article
Kidney International, ISSN 0085-2538, 07/2015, Volume 88, Issue 1, pp. 17 - 27
Journal Article