X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
dnm1 (39) 39
index medicus (26) 26
cell biology (16) 16
humans (15) 15
mitochondria (13) 13
mitochondria - metabolism (13) 13
yeast (13) 13
animals (12) 12
dynamin (11) 11
saccharomyces-cerevisiae (11) 11
fusion (10) 10
mutation (10) 10
division (9) 9
gtp phosphohydrolases - metabolism (9) 9
mitochondrial proteins - metabolism (9) 9
fission (8) 8
gtpase (8) 8
mitochondrial dna (8) 8
biochemistry & molecular biology (7) 7
drp1 (7) 7
mitochondrial dynamics (7) 7
multidisciplinary sciences (7) 7
proteins (7) 7
article (6) 6
dogs (6) 6
fis1 (6) 6
fungal proteins - genetics (6) 6
mitochondria - ultrastructure (6) 6
mitochondrial proteins - genetics (6) 6
protein (6) 6
wd repeat protein (6) 6
apoptosis (5) 5
cell division (5) 5
dnm1 mutation (5) 5
fungal proteins - metabolism (5) 5
gene (5) 5
gtp phosphohydrolases - genetics (5) 5
peroxisomes - metabolism (5) 5
saccharomyces cerevisiae - metabolism (5) 5
saccharomyces cerevisiae proteins - metabolism (5) 5
biological sciences (4) 4
dog diseases - genetics (4) 4
dynamin i - genetics (4) 4
dynamin-related protein (4) 4
dynamins (4) 4
dynamins - metabolism (4) 4
epilepsy (4) 4
exercise (4) 4
female (4) 4
genetic aspects (4) 4
labrador retriever (4) 4
male (4) 4
mammalian-cells (4) 4
mitochondria - physiology (4) 4
mitochondrial division (4) 4
mitochondrial fission (4) 4
mitochondrial fusion (4) 4
mitochondrial proteins (4) 4
outer-membrane (4) 4
pcr (4) 4
phenotype (4) 4
physiological aspects (4) 4
saccharomyces cerevisiae - cytology (4) 4
saccharomyces cerevisiae - genetics (4) 4
saccharomyces cerevisiae proteins - genetics (4) 4
sequencing (4) 4
veterinary sciences (4) 4
yeasts (4) 4
adaptor proteins, signal transducing (3) 3
adolescent (3) 3
budding yeast (3) 3
carrier proteins - metabolism (3) 3
cells (3) 3
clinical neurology (3) 3
cloning, molecular (3) 3
deletion (3) 3
disruption (3) 3
dnm1 gene (3) 3
dnm1 protein (3) 3
dynamin i (3) 3
dynamin i - metabolism (3) 3
dynamin-related gtpase (3) 3
exercise-induced collapse (3) 3
fzo1 (3) 3
fzo1 gene (3) 3
fzo1 protein (3) 3
genes, fungal (3) 3
genetic disorders (3) 3
gtp phosphohydrolases - chemistry (3) 3
gtp phosphohydrolases - physiology (3) 3
guanosine triphosphate - metabolism (3) 3
infant (3) 3
mdv1 (3) 3
microscopy, electron (3) 3
mitochondrial dynamics - physiology (3) 3
mitophagy (3) 3
models, biological (3) 3
molecular biology (3) 3
molecular sequence data (3) 3
mutations (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


CIENCIA RURAL, ISSN 0103-8478, 09/2014, Volume 44, Issue 9, pp. 1629 - 1631
The exercise-induced collapse (EIC) is a hereditary disease characterized by muscle weakness, impaired locomotion and collapse after intense exercise. This... 
mutation | AGRONOMY | STRENUOUS EXERCISE | dogs | exercise | DNM1 MUTATION | DNM1 | sequencing
Journal Article
by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
Journal Article
Pesquisa Veterinária Brasileira, ISSN 0100-736X, 05/2015, Volume 35, Issue 5, pp. 486 - 490
Resumo:O colapso induzido pelo exercício (EIC) é considerado uma síndrome autossômica recessiva que afeta principalmente cães da raça Labrador Retriever. A... 
Labrador Retriever | sequenciamento | exercício | DNM1 | PCR | Cães
Journal Article
Ciencia Rural, ISSN 0103-8478, 09/2014, Volume 44, Issue 9, pp. 1629 - 1631
O colapso induzido pelo exercício (EIC) é uma enfermidade hereditária caracterizada por fraqueza muscular, dificuldade de locomoção e colapso após atividade... 
Exercise | Mutation | Sequencing | DNM1 | Dogs | AGRONOMY
Journal Article
Ciência Rural, ISSN 1678-4596, 09/2014, Volume 44, Issue 9, pp. 1629 - 1631
O colapso induzido pelo exercício (EIC) é uma enfermidade hereditária caracterizada por fraqueza muscular, dificuldade de locomoção e colapso após atividade... 
exercício | sequenciamento | mutação | cães | DNM1
Journal Article
BBA - Molecular Cell Research, ISSN 0167-4889, 10/2015, Volume 1853, Issue 10, pp. 2766 - 2774
Mitochondria fulfill central cellular functions including energy metabolism, iron-sulfur biogenesis, and regulation of apoptosis and calcium homeostasis.... 
Atg32 | Ubiquitination | Mgm1 | Mitophagy | Mitochondrial dynamics | Dnm1 | COMPLEX | PROTEIN | FUSION | INNER MEMBRANE | AUTOPHAGIC DEGRADATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | STRESS-RESPONSE | Dnml | CELL BIOLOGY | YEAST | TOR | FISSION | Mgml | MTDNA MUTATIONS | Sulfur compounds | Biosynthesis | Mitochondrial DNA
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 11/1999, Volume 147, Issue 4, pp. 699 - 706
Journal Article
Autophagy, ISSN 1554-8627, 05/2017, Volume 13, Issue 5, pp. 980 - 981
Mitochondrial autophagy (mitophagy) is thought to be a multi-step pathway wherein mitochondria are first divided into small fragments, which are subsequently... 
mitophagy | autophagy | DNM1L | mitochondria | Dnm1 | mitochondrial division | CELL BIOLOGY | Animals | Mitochondrial Proteins - metabolism | Humans | Autophagy - physiology | Mitochondria - metabolism | Autophagosomes - metabolism | Mitochondrial Degradation - physiology | Mitochondrial Dynamics - physiology
Journal Article
Journal Article
Journal of Sichuan University (Medical Science Edition), ISSN 1672-173X, 05/2018, Volume 49, Issue 3, pp. 347 - 351
Journal Article
PESQUISA VETERINARIA BRASILEIRA, ISSN 0100-736X, 05/2015, Volume 35, Issue 5, pp. 486 - 490
The exercise-induced collapse (EIC) is considered an autosomal recessive syndrome that mainly affects Labrador Retriever dogs. The disease is characterized by... 
Labrador Retriever | MUTATION | exercise | VETERINARY SCIENCES | Dog | DNM1 | PCR | sequencing
Journal Article