X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (12890) 12890
Newspaper Article (2120) 2120
Publication (1840) 1840
Book Chapter (246) 246
Book Review (157) 157
Magazine Article (81) 81
Trade Publication Article (61) 61
Conference Proceeding (50) 50
Dissertation (37) 37
Reference (30) 30
Book / eBook (25) 25
Government Document (16) 16
Web Resource (14) 14
Data Set (10) 10
Report (5) 5
Journal / eJournal (1) 1
Paper (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (7868) 7868
index medicus (5775) 5775
animals (5150) 5150
neurosciences (4165) 4165
huntington's disease (4117) 4117
huntingtons disease (4039) 4039
huntingtons-disease (3885) 3885
male (3563) 3563
huntington disease - genetics (3486) 3486
female (3152) 3152
mice (2793) 2793
adult (2033) 2033
neurodegeneration (1923) 1923
proteins (1906) 1906
mutation (1894) 1894
middle aged (1859) 1859
biochemistry & molecular biology (1806) 1806
disease models, animal (1795) 1795
clinical neurology (1763) 1763
huntington's chorea (1671) 1671
huntington disease (1659) 1659
brain (1612) 1612
huntington disease - pathology (1583) 1583
huntington disease - metabolism (1570) 1570
genetics & heredity (1559) 1559
nerve tissue proteins - genetics (1549) 1549
neurodegenerative diseases (1540) 1540
neurology (1502) 1502
nervous system diseases (1434) 1434
huntingtin protein (1413) 1413
neurons (1294) 1294
analysis (1250) 1250
research (1239) 1239
gene expression (1236) 1236
nervous system (1228) 1228
cell biology (1187) 1187
mice, transgenic (1185) 1185
huntington disease - physiopathology (1152) 1152
mutant huntingtin (1139) 1139
alzheimers-disease (1125) 1125
parkinsons-disease (1110) 1110
huntington’s disease (1077) 1077
nuclear proteins - genetics (1035) 1035
nerve tissue proteins - metabolism (1029) 1029
aged (1020) 1020
mouse model (1000) 1000
genetics (995) 995
rats (974) 974
neurons - metabolism (973) 973
huntingtin (970) 970
article (943) 943
gene (939) 939
polyglutamine (898) 898
genetic aspects (895) 895
disease (876) 876
transgenic mice (859) 859
rodents (854) 854
multidisciplinary sciences (816) 816
huntington disease - diagnosis (813) 813
alzheimer's disease (806) 806
apoptosis (797) 797
medical research (796) 796
parkinson's disease (788) 788
research article (786) 786
brain - metabolism (769) 769
oxidative stress (768) 768
genes (759) 759
trinucleotide repeats (754) 754
expression (747) 747
medicine (745) 745
brain - pathology (729) 729
gene therapy (723) 723
alzheimers disease (674) 674
nuclear proteins - metabolism (671) 671
physiological aspects (669) 669
studies (634) 634
phenotype (633) 633
biology (616) 616
psychiatry (600) 600
basal ganglia (598) 598
neurons - pathology (594) 594
gene-expression (584) 584
mental disorders (581) 581
neuroscience (579) 579
pathology (578) 578
trinucleotide repeat (578) 578
mice, inbred c57bl (577) 577
cells, cultured (567) 567
health aspects (566) 566
pathogenesis (563) 563
amyotrophic lateral sclerosis (546) 546
age (538) 538
brain research (534) 534
amyotrophic-lateral-sclerosis (531) 531
pharmacology & pharmacy (524) 524
protein (520) 520
science (519) 519
disease progression (518) 518
degeneration (512) 512
animal models (511) 511
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (12) 12
UofT at Mississauga - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
New College (Ivey) - Stacks (1) 1
Online Resources - Online (1) 1
Scarborough Hospital - Online (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
UTL at Downsview - May be requested (1) 1
UofT Schools - Stacks (1) 1
UofT at Mississauga - Novelties Reading Area (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (15207) 15207
French (51) 51
Japanese (50) 50
Spanish (49) 49
German (48) 48
Chinese (21) 21
Russian (19) 19
Polish (11) 11
Czech (5) 5
Swedish (4) 4
Dutch (3) 3
Norwegian (3) 3
Turkish (3) 3
Croatian (2) 2
Hebrew (2) 2
Hungarian (2) 2
Portuguese (2) 2
Slovak (2) 2
Danish (1) 1
Italian (1) 1
Korean (1) 1
Serbian (1) 1
Slovenian (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Biomedicine & Pharmacotherapy, ISSN 0753-3322, 2016, Volume 84, pp. 514 - 525
Graphical abstract 
Internal Medicine | Medical Education | Huntington’s disease | Apoptotic markers | Mitochondrial dysfunction | Histopathology | Chrysin | 3-Nitropropionic acid | Huntington's disease | MEDICINE, RESEARCH & EXPERIMENTAL | TOXIN | NEURONAL CELL-DEATH | FLAVONOIDS | MODEL | QUINOLINIC ACID | PROPOLIS | INHIBITION | PHARMACOLOGY & PHARMACY | HUNTINGTONS-DISEASE | BRAIN | MODULATION | Up-Regulation | Mitochondrial Swelling - drug effects | Rats, Wistar | Apoptosis - drug effects | Basal Ganglia - metabolism | Huntington Disease - psychology | Mitochondrial Diseases - metabolism | Motor Activity - drug effects | Male | Postural Balance - drug effects | Dose-Response Relationship, Drug | Mitochondrial Diseases - psychology | Proto-Oncogene Proteins c-bcl-2 - metabolism | Neuroprotective Agents - pharmacology | Time Factors | bcl-Associated Death Protein - metabolism | Behavior, Animal - drug effects | Flavonoids - pharmacology | Huntington Disease - physiopathology | bcl-2-Associated X Protein - genetics | Disease Models, Animal | Biomarkers - metabolism | bcl-Associated Death Protein - genetics | Mitochondrial Diseases - prevention & control | Huntington Disease - prevention & control | Down-Regulation | bcl-2-Associated X Protein - metabolism | Basal Ganglia - pathology | Maze Learning - drug effects | Huntington Disease - metabolism | Animals | Signal Transduction - drug effects | Nitro Compounds | Propionates | Oxidative Stress - drug effects | Mitochondrial Diseases - physiopathology | Nerve Degeneration | Proto-Oncogene Proteins c-bcl-2 - genetics | Basal Ganglia - drug effects | Genes | Apoptosis | Antioxidants | Flavonoids | Enzyme inhibitors | Flavones | RNA | Bioflavonoids | Genetic research | Superoxide
Journal Article
by Imanishi, Tadashi and Itoh, Takeshi and Suzuki, Yutaka and O'Donovan, Claire and Fukuchi, Satoshi and Koyanagi, Kanako O and Barrero, Roberto A and Tamura, Takuro and Yamaguchi-Kabata, Yumi and Tanino, Motohiko and Yura, Kei and Miyazaki, Satoru and Ikeo, Kazuho and Homma, Keiichi and Kasprzyk, Arek and Nishikawa, Tetsuo and Hirakawa, Mika and Thierry-Mieg, Jean and Thierry-Mieg, Danielle and Ashurst, Jennifer and Jia, Libin and Nakao, Mitsuteru and Thomas, Michael A and Mulder, Nicola and Karavidopoulou, Youla and Jin, Lihua and Kim, Sangsoo and Yasuda, Tomohiro and Lenhard, Boris and Eveno, Eric and Suzuki, Yoshiyuki and Yamasaki, Chisato and Takeda, Jun-Ichi and Gough, Craig and Hilton, Phillip and Fujii, Yasuyuki and Sakai, Hiroaki and Tanaka, Susumu and Amid, Clara and Bellgard, Matthew and de Fatima Bonaldo, Maria and Bono, Hidemasa and Bromberg, Susan K and Brookes, Anthony J and Bruford, Elspeth and Carninci, Piero and Chelala, Claude and Couillault, Christine and de Souza, Sandro J and Debily, Marie-Anne and Devignes, Marie-Dominique and Dubchak, Inna and Endo, Toshinori and Estreicher, Anne and Eyras, Eduardo and Fukami-Kobayashi, Kaoru and Gopinath, Gopal R and Graudens, Esther and Hahn, Yoonsoo and Han, Michael and Han, Ze-Guang and Hanada, Kousuke and Hanaoka, Hideki and Harada, Erimi and Hashimoto, Katsuyuki and Hinz, Ursula and Hirai, Momoki and Hishiki, Teruyoshi and Hopkinson, Ian and Imbeaud, Sandrine and Inoko, Hidetoshi and Kanapin, Alexander and Kaneko, Yayoi and Kasukawa, Takeya and Kelso, Janet and Kersey, Paul and Kikuno, Reiko and Kimura, Kouichi and Korn, Bernhard and Kuryshev, Vladimir and Makalowska, Izabela and Makino, Takashi and Mano, Shuhei and Mariage-Samson, Regine and Mashima, Jun and Matsuda, Hideo and Mewes, Hans-Werner and Minoshima, Shinsei and Nagai, Keiichi and Nagasaki, Hideki and Nagata, Naoki and Nigam, Rajni and Ogasawara, Osamu and Ohara, Osamu and Ohtsubo, Masafumi and Okada, Norihiro and Okido, Toshihisa and Oota, Satoshi and Ota, Motonori and Ota, Toshio and ... and Tidigare Institutioner (före 2005) and KTH and Bioteknologi
PLoS Biology, ISSN 1544-9173, 2004, Volume 2, Issue 6, pp. 856 - 875
The human genome sequence defines our inherent biological potential; the realization of the biology encoded therein requires knowledge of the function of each... 
MESSENGER-RNAS | COMPLETE GENOME SEQUENCE | LARGE PROTEINS | DROSOPHILA-MELANOGASTER | UNTRANSLATED REGIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGY | SUBCELLULAR-LOCALIZATION | FUNCTIONAL ANNOTATION | EXPRESSED SEQUENCE TAGS | HUNTINGTONS-DISEASE | SINGLE NUCLEOTIDE POLYMORPHISMS | Protein Structure, Tertiary | Computational Biology - methods | Alternative Splicing - genetics | Humans | DNA, Complementary - genetics | Databases, Genetic | Genes - genetics | Open Reading Frames - genetics | Microsatellite Repeats - genetics | Polymorphism, Genetic | Genes - physiology | Polymorphism, Single Nucleotide | Internet | Genome, Human | Proteins | Genomics | Genetics | Biology | Genomes | Gene expression | Polymorphism | Gens | ADN | Computer Science | Other | Gene Therapy | Bioinformatics | Homo (Human) | Computational Biology | human genetics | RNA | Alternative Splicing | single nucleotide polymorphism | structure analysis | gene location | gene deletion | protein structure | genetic transcription | genome analysis | protein | gene mapping | Biochemistry and Molecular Biology | Microsatellite Repeats | Biological Sciences | biology | gene insertion | gene | Tertiary | physiology | article | RNA analysis | Naturvetenskap | genetic analysis | qualitative analysis | prediction | metabolism | genetic polymorphism | Genes | Open Reading Frames | alternative RNA splicing | reliability | Genetic | gene identification | international cooperation | open reading frame | genetic database | protein tertiary structure | Single Nucleotide | Complementary | data base | complementary DNA | cellular distribution | genetics | Databases | insertion sequences | sequence analysis | Natural Sciences | human | gene structure | phenotype | validation process | gene cassette | gene sequence | gene function | genetic variability | gene locus | nucleotide sequence | genome | controlled study | Biokemi och molekylärbiologi | Biologiska vetenskaper | DNA | organization | molecular cloning | microsatellite DNA | methodology
Journal Article
Human molecular genetics, ISSN 0964-6906, 04/2016, Volume 25, Issue 1, pp. R18 - R26
The concept of orphan drugs for treatment of orphan genetic diseases is perceived enthusiastically at present, and this is leading to research investment on... 
NONSENSE-MUTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | DUCHENNE MUSCULAR-DYSTROPHY | MICE | THERAPIES | CYSTIC-FIBROSIS | SUPPRESSION | ANTISENSE OLIGONUCLEOTIDES | HUNTINGTONS-DISEASE | ATALUREN | MOLECULAR-MECHANISMS | Gene Targeting | Humans | Rare Diseases - drug therapy | Genetic Diseases, Inborn - drug therapy | Invited Reviews
Journal Article
Journal Article