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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 | 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 | Computational Biology | 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