X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (28212) 28212
Publication (4279) 4279
Book Review (2821) 2821
Newspaper Article (414) 414
Book Chapter (379) 379
Conference Proceeding (158) 158
Newsletter (90) 90
Dissertation (39) 39
Magazine Article (26) 26
Trade Publication Article (18) 18
Book / eBook (16) 16
Reference (7) 7
Web Resource (5) 5
Data Set (1) 1
Presentation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (25233) 25233
animals (24261) 24261
zebrafish (19135) 19135
humans (7648) 7648
zebrafish - genetics (7451) 7451
developmental biology (6984) 6984
zebrafish - embryology (6365) 6365
zebrafish proteins - genetics (5863) 5863
cell biology (5486) 5486
expression (5241) 5241
gene expression (5186) 5186
zebrafish proteins - metabolism (4764) 4764
mice (4678) 4678
biochemistry & molecular biology (4574) 4574
molecular sequence data (4569) 4569
gene expression regulation, developmental (4473) 4473
analysis (4440) 4440
proteins (4270) 4270
zebrafish - metabolism (4189) 4189
genes (3993) 3993
research (3920) 3920
amino acid sequence (3767) 3767
mutation (3601) 3601
genetic aspects (3534) 3534
female (3446) 3446
multidisciplinary sciences (3323) 3323
article (3318) 3318
research article (3314) 3314
genetics & heredity (3268) 3268
signal transduction (3221) 3221
fish (3078) 3078
embryos (3061) 3061
male (3021) 3021
physiological aspects (2913) 2913
animals, genetically modified (2775) 2775
biology (2759) 2759
base sequence (2677) 2677
gene-expression (2628) 2628
gene (2520) 2520
neurosciences (2377) 2377
medicine (2359) 2359
cells (2289) 2289
in situ hybridization (2287) 2287
genetics (2243) 2243
zebrafish proteins (2222) 2222
phylogeny (2173) 2173
science (2050) 2050
embryonic development (2010) 2010
danio-rerio (1991) 1991
embryo, nonmammalian - metabolism (1955) 1955
molecular biology (1930) 1930
in-vivo (1915) 1915
protein (1872) 1872
genomics (1785) 1785
phenotype (1743) 1743
toxicology (1727) 1727
morphogenesis (1720) 1720
rna, messenger - metabolism (1719) 1719
differentiation (1718) 1718
animal structures (1708) 1708
transcription factors - genetics (1699) 1699
zebrafish - physiology (1693) 1693
vertebrates (1673) 1673
zebra fish (1639) 1639
cloning, molecular (1623) 1623
genomes (1609) 1609
brain (1574) 1574
evolution (1573) 1573
life sciences (1571) 1571
sequence homology, amino acid (1570) 1570
zoology (1556) 1556
disease models, animal (1550) 1550
genetic research (1547) 1547
identification (1508) 1508
rna, messenger - genetics (1500) 1500
rna (1473) 1473
apoptosis (1427) 1427
neurons (1383) 1383
zebrafish - growth & development (1348) 1348
transcription factors - metabolism (1336) 1336
embryonic structures (1330) 1330
cell differentiation (1306) 1306
sequence alignment (1302) 1302
embryo, nonmammalian (1301) 1301
wnt proteins (1296) 1296
gene expression profiling (1267) 1267
fishes (1257) 1257
transcription factors (1256) 1256
gene expression regulation (1245) 1245
physiology (1237) 1237
cancer (1205) 1205
mutations (1198) 1198
drosophila (1189) 1189
cell line (1180) 1180
mouse (1179) 1179
homeodomain proteins - genetics (1172) 1172
reverse transcriptase polymerase chain reaction (1170) 1170
stem cells (1142) 1142
rodents (1135) 1135
animal models (1112) 1112
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (28768) 28768
Japanese (53) 53
Chinese (52) 52
French (23) 23
Russian (4) 4
Spanish (2) 2
German (1) 1
Polish (1) 1
Portuguese (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Fitzgerald, T.W and Gerety, S.S and Jones, W.D and Van Kogelenberg, M and King, D.A and McRae, J and Morley, K.I and Parthiban, V and Al-Turki, S and Ambridge, K and Barrett, D.M and Bayzetinova, T and Clayton, S and Coomber, E.L and Gribble, S and Jones, P and Krishnappa, N and Mason, L.E and Middleton, A and Miller, R and Prigmore, E and Rajan, D and Sifrim, A and Tivey, A.R and Ahmed, M and Akawi, N and Andrews, R and Anjum, U and Archer, H and Armstrong, R and Balasubramanian, M and Banerjee, R and Baralle, D and Batstone, P and Baty, D and Bennett, C and Berg, J and Bernhard, B and Bevan, A.P and Blair, E and Blyth, M and Bohanna, D and Bourdon, L and Bourn, D and Brady, A and Bragin, E and Brewer, C and Brueton, L and Brunstrom, K and Bumpstead, S.J and Bunyan, D.J and Burn, J and Burton, J and Canham, N and Castle, B and Chandler, K and Clasper, S and Clayton-Smith, J and Cole, T and Collins, A and Collinson, M.N and Connell, F and Cooper, N and Cox, H and Cresswell, L and Cross, G and Crow, Y and D'Alessandro, M and Dabir, T and Davidson, R and Davies, S and Dean, J and Deshpande, C and Devlin, G and Dixit, A and Dominiczak, A and Donnelly, C and Donnelly, D and Douglas, A and Duncan, A and Eason, J and Edkins, S and Ellard, S and Ellis, P and Elmslie, F and Evans, K and Everest, S and Fendick, T and Fisher, R and Flinter, F and Foulds, N and Fryer, A and Fu, B and Gardiner, C and Gaunt, L and Ghali, N and Gibbons, R and Gomes Pereira, S.L and Goodship, J and Goudie, D and ... and Deciphering Dev Disorders Study and Deciphering Developmental Disorders Study and The Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 03/2015, Volume 519, Issue 7542, pp. 223 - 228
Despite three decades of successful, predominantly phenotype-driven discovery of the genetic causes of monogenic disorders(1), up to half of children with... 
INTELLECTUAL DISABILITY | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | MODEL | AUTISM SPECTRUM DISORDERS | COPY-NUMBER VARIATION | CHILDREN | Rare Diseases - genetics | Humans | Parents | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Dynamin I - genetics | Mutation, Missense - genetics | Polycomb Repressive Complex 1 - genetics | Gene Expression Regulation, Developmental | Transposases - genetics | Female | Nuclear Proteins - genetics | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Guanine Nucleotide Exchange Factors - genetics | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | United Kingdom | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Zebrafish - genetics | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Animals | Adolescent | Chromosome Aberrations | Genes, Dominant - genetics | Usage | Genomics | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Studies | Hypotheses | Genes | Developmental psychology | Families & family life | Genomes | Mutation | Children & youth | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 507, Issue 7492, pp. 371 - 375
Journal Article
Circulation, ISSN 0009-7322, 10/2014, Volume 130, Issue 15, pp. 1225 - 1235
BACKGROUND—Atrial fibrillation (AF) affects >30 million individuals worldwide and is associated with an increased risk of stroke, heart failure, and death. AF... 
Atrial fibrillation | Genetics | Zebrafish | Gene expression | Single nucleotide | Epidemiology | Polymorphism | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK-FACTORS | METAANALYSIS | VARIANTS | polymorphism | LOCI | epidemiology | atrial fibrillation | PR INTERVAL | genetics | single nucleotide | PERIPHERAL VASCULAR DISEASE | PRAVASTATIN | zebrafish | HEART-RATE | ISCHEMIC-STROKE | gene expression | ONSET | GENOME-WIDE ASSOCIATION | T-Box Domain Proteins - physiology | Humans | Middle Aged | Male | Genetic Loci - physiology | Atrial Fibrillation - physiopathology | Ubiquitin-Protein Ligases - physiology | Gene Knockdown Techniques | Repressor Proteins - physiology | Muscle Proteins | Connexin 43 - physiology | Female | Nuclear Proteins - genetics | Connexin 43 - genetics | Transcription Factors - physiology | Europe | Japan | Repressor Proteins - genetics | Atrial Fibrillation - ethnology | Genotype | Chromosome Mapping | Transcription Factors - genetics | Atrial Fibrillation - genetics | T-Box Domain Proteins - genetics | Homeodomain Proteins - genetics | Zebrafish Proteins - physiology | Animals | Genetic Predisposition to Disease - ethnology | Aged | Nuclear Proteins - physiology | Zebrafish Proteins - genetics | Homeodomain Proteins - physiology | Quantitative Trait Loci | Ubiquitin-Protein Ligases - genetics | Stroke (Disease) | Care and treatment | Usage | Analysis | Genetic transcription | Diagnosis | Nucleotides | Risk factors | Index Medicus | Abridged Index Medicus
Journal Article
Nature, ISSN 0028-0836, 05/2012, Volume 484, Issue 7397, pp. 195 - 202
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 496, Issue 7446, pp. 498 - 503
Journal Article
Nature Cell Biology, ISSN 1465-7392, 2015, Volume 17, Issue 8, pp. 1074 - 1087
Defects in primary cilium biogenesis underlie the ciliopathies, a growing group of genetic disorders. We describe a whole-genome siRNA-based reverse genetics... 
JOUBERT-SYNDROME | RPGRIP1 | TRANSPORT | CENTRIOLE BIOGENESIS | PROTEIN | C-ELEGANS | MUTATIONS | PHOTORECEPTOR CELLS | MASTER REGULATOR | PRIMARY CILIA | CELL BIOLOGY | Humans | Pregnancy Proteins - genetics | Databases, Genetic | Suppressor Factors, Immunologic - genetics | Photoreceptor Cells - ultrastructure | Pregnancy Proteins - metabolism | Ellis-Van Creveld Syndrome - genetics | Cerebellum - abnormalities | Genetic Testing - methods | Suppressor Factors, Immunologic - metabolism | Membrane Proteins - deficiency | Transfection | RNA Interference | HEK293 Cells | Kidney Diseases, Cystic - genetics | Genomics - methods | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Caenorhabditis elegans - metabolism | Cilia - pathology | Caenorhabditis elegans - genetics | Membrane Proteins - genetics | Mice, Inbred C57BL | Abnormalities, Multiple | Genetic Markers | Eye Abnormalities - genetics | Cilia - metabolism | Zebrafish - genetics | Cilia - genetics | Mice, Knockout | Proteins - genetics | Caenorhabditis elegans - ultrastructure | Phenotype | Animals | Cerebellar Diseases - genetics | Ciliary Motility Disorders - pathology | Proteins - metabolism | Photoreceptor Cells - metabolism | Zebrafish - metabolism | Retina - abnormalities | High-Throughput Nucleotide Sequencing | Ciliary Motility Disorders - metabolism | Mutation | Ciliary Motility Disorders - genetics | RNA | Cilia and ciliary motion | Genetic research | Biosynthesis | Genetic aspects | Research | Gene expression | Properties | Index Medicus | reverse genetics | cilia | ciliopathies | Joubert syndrome | whole-genome siRNA screen | Jeune syndrome
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2015, Volume 47, Issue 8, pp. 926 - 932
Dominant optic atrophy (DOA)(1,2) and axonal peripheral neuropathy (Charcot-Marie-Tooth type 2, or CMT2)(3) are hereditary neurodegenerative disorders most... 
MEMBRANE-FUSION | MITOCHONDRIAL FUSION | OUTER-MEMBRANE | RECRUITMENT | ZEBRAFISH | OPA1 | MITOFUSIN-2 | GENETICS & HEREDITY | DYNAMICS | CARRIER PROTEIN | MOTONEURONS | Humans | Optic Atrophy, Autosomal Dominant - metabolism | Embryo, Nonmammalian - metabolism | Phosphate Transport Proteins - metabolism | Cercopithecus aethiops | Embryo, Nonmammalian - embryology | Male | Mitochondrial Proteins - genetics | Zebrafish - embryology | Charcot-Marie-Tooth Disease - genetics | RNA Interference | Mitochondrial Proteins - metabolism | HEK293 Cells | Muscle Proteins - metabolism | Female | Membrane Proteins - metabolism | Optic Atrophy, Autosomal Dominant - pathology | Phosphate Transport Proteins - genetics | Charcot-Marie-Tooth Disease - metabolism | Microscopy, Electron, Transmission | Genetic Predisposition to Disease - genetics | Animals, Genetically Modified | Membrane Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Sequence Analysis, DNA | Mitochondrial Membranes - metabolism | Muscle Proteins - genetics | Microscopy, Confocal | Exome - genetics | Animals | Pedigree | Embryo, Nonmammalian - ultrastructure | Zebrafish - metabolism | Optic Atrophy, Autosomal Dominant - genetics | Saccharomyces cerevisiae Proteins - metabolism | Protein Binding | Mutation | COS Cells | Development and progression | Genetic aspects | Optic atrophy | Gene mutations | Identification and classification | Health aspects | Proteins | Neurodegeneration | Genes | Neurological disorders | Index Medicus
Journal Article