X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3071) 3071
Publication (640) 640
Book Chapter (29) 29
Book Review (23) 23
Conference Proceeding (12) 12
Dissertation (2) 2
Government Document (2) 2
Magazine Article (2) 2
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (1601) 1601
humans (1574) 1574
index medicus (1525) 1525
biochemistry & molecular biology (776) 776
ankyrin (769) 769
mice (735) 735
molecular sequence data (715) 715
proteins (699) 699
amino acid sequence (630) 630
ankyrin repeat (615) 615
cell biology (587) 587
ankyrins - genetics (560) 560
male (502) 502
female (469) 469
mutation (461) 461
ankyrins - metabolism (436) 436
protein binding (400) 400
gene expression (382) 382
research (349) 349
genetic aspects (334) 334
expression (333) 333
rats (330) 330
article (325) 325
multidisciplinary sciences (314) 314
base sequence (311) 311
genes (306) 306
neurosciences (305) 305
signal transduction (304) 304
genetics & heredity (299) 299
analysis (285) 285
protein (285) 285
research article (285) 285
protein structure, tertiary (258) 258
physiological aspects (246) 246
cell line (243) 243
binding sites (227) 227
models, molecular (224) 224
ankyrins (221) 221
gene (221) 221
cells, cultured (216) 216
sequence homology, amino acid (205) 205
membrane proteins - genetics (189) 189
medicine (187) 187
cells (186) 186
ankyrin repeats (183) 183
activation (182) 182
neurons (181) 181
cloning, molecular (178) 178
biology (177) 177
drosophila (174) 174
spectrin (173) 173
cytoskeleton (172) 172
identification (172) 172
genetics (171) 171
phosphorylation (169) 169
ankyrins - chemistry (166) 166
science (166) 166
membrane proteins - metabolism (165) 165
binding (163) 163
phenotype (163) 163
adult (162) 162
ankyrin repeat - genetics (158) 158
mice, inbred c57bl (158) 158
mice, knockout (157) 157
sequence alignment (157) 157
biophysics (151) 151
life sciences (148) 148
hematology (145) 145
transcription factors (145) 145
rna, messenger - genetics (143) 143
rna, messenger - metabolism (143) 143
gene expression regulation (142) 142
genomes (141) 141
ankyrin repeat protein (140) 140
developmental biology (139) 139
localization (138) 138
genomics (134) 134
protein conformation (132) 132
transfection (131) 131
membrane proteins (130) 130
physiology (129) 129
phylogeny (126) 126
ankyrin-g (125) 125
gene-expression (123) 123
cancer (122) 122
apoptosis (121) 121
polymerase chain reaction (119) 119
carrier proteins - genetics (117) 117
health aspects (117) 117
mutations (117) 117
recombinant fusion proteins - metabolism (117) 117
biochemistry (114) 114
molecular biology (114) 114
spectrin - genetics (114) 114
carrier proteins - metabolism (113) 113
crystal-structure (113) 113
genetic research (113) 113
nervous system (112) 112
dna (111) 111
middle aged (111) 111
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3046) 3046
Japanese (11) 11
Chinese (8) 8
French (7) 7
Russian (4) 4
Spanish (4) 4
German (2) 2
Italian (2) 2
Polish (2) 2
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Neuroscience, ISSN 1097-6256, 08/2014, Volume 17, Issue 9, pp. 1156 - 1163
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, p. e0133037
Background The use of next-generation sequencing enables a rapid analysis of many genes associated with sudden cardiac death in diseases like Brugada Syndrome.... 
NA(V)1.5 | ANKYRIN-G | COMMON POLYMORPHISM | MULTIDISCIPLINARY SCIENCES | COMPOUND | SUDDEN CARDIAC DEATH | PHENOTYPE | NOISE | LONG-QT SYNDROME | MUTATIONS | RIGHT-VENTRICULAR CARDIOMYOPATHY/DYSPLASIA | Brugada Syndrome - genetics | Brugada Syndrome - diagnosis | Genetic Testing | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Male | Calsequestrin - genetics | Death, Sudden, Cardiac | Genetic Variation | A Kinase Anchor Proteins - genetics | gamma Catenin | Desmoplakins - genetics | Clinical Decision-Making | Adult | Female | Retrospective Studies | NAV1.5 Voltage-Gated Sodium Channel - genetics | Arrhythmias, Cardiac - genetics | Desmoglein 2 - genetics | Penetrance | Potassium Channels, Inwardly Rectifying - genetics | Sequence Analysis, DNA | Ryanodine Receptor Calcium Release Channel - genetics | Pedigree | Ankyrins - genetics | High-Throughput Nucleotide Sequencing | Cohort Studies | Cardiac arrhythmia | Copy number | Genes | Insertion | Ryanodine receptors | Genetic screening | Gene sequencing | Complexity | Proteins | Clonal deletion | Defibrillators | Genetic analysis | Electrocardiography | Deletion | Potassium channels (voltage-gated) | Heart diseases | Ion channels (cyclic nucleotide-gated) | Potassium channels (inwardly-rectifying) | Decision making | Data processing | Genetic diversity | Patients | Coronary artery disease | Substrates | Diseases | Genetic variance | KCNQ1 protein | Mutation | Variation | Malalties | Heart | Aspectes genètics | Arítmia | Arrhythmia | Cor | Genetic aspects
Journal Article
Nature, ISSN 0028-0836, 06/2010, Volume 465, Issue 7298, pp. 632 - 636
Journal Article
Forensic Science International, ISSN 0379-0738, 12/2018, Volume 293, pp. 70 - 76
Cases of sudden cardiac death (SCD) in young and apparently healthy individuals represent a devastating event in affected families. Hereditary arrhythmia... 
Genetics | Massive parallel sequencing | Sudden cardiac death | Arrhythmia syndromes | Sudden death | BRUGADA SYNDROME | VARIANTS | MEDICINE, LEGAL | UNEXPLAINED DEATH | EUROPEAN-SOCIETY | HYPERTROPHIC CARDIOMYOPATHY | RECOMMENDATIONS | MOLECULAR AUTOPSY | CARDIAC DEATH | EPIDEMIOLOGY | CHANNELOPATHIES | Cardiac Myosins - genetics | Humans | Connectin - genetics | Myosin Heavy Chains - genetics | Infant | Male | Death, Sudden, Cardiac - etiology | Sequence Analysis, DNA | Genetic Variation | Young Adult | Cardiomyopathies - genetics | Channelopathies - genetics | Calcium Channels, L-Type - genetics | Dystrophin - genetics | Hypertrophy, Left Ventricular - pathology | Ankyrins - genetics | Forensic Genetics | Adult | Female | High-Throughput Nucleotide Sequencing | alpha Catenin - genetics | Microfilament Proteins - genetics | Arrhythmia | Demographic aspects | Cardiac arrest | Causes of | Youth | Genetic aspects | Teenagers | Health aspects | Death of | Heart | Cardiac arrhythmia | Cardiomyopathy | Epilepsy | Genes | Cardiovascular disease | Family medical history | Genetic screening | Gene sequencing | Analgesics | Autopsy | Genetic analysis | Deoxyribonucleic acid--DNA | Genetic disorders | Forensic science | Legal medicine | Mortality | Preventive medicine | Disease prevention | Studies | Pathology | Sleep | Genetic counseling | Death
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2015, Volume 96, Issue 2, pp. 245 - 257
Journal Article
Human Mutation, ISSN 1059-7794, 11/2009, Volume 30, Issue 11, pp. 1486 - 1511
Journal Article