X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (35) 35
index medicus (35) 35
animals (27) 27
genetics & heredity (24) 24
genetic aspects (18) 18
genetics (18) 18
mutation (18) 18
zebrafish (15) 15
article (14) 14
female (14) 14
research (14) 14
proteins (13) 13
male (12) 12
genes (11) 11
mice (11) 11
phenotype (11) 11
child (10) 10
life sciences (10) 10
zebrafish - genetics (10) 10
child, preschool (9) 9
gene mutations (9) 9
mutations (9) 9
autism (8) 8
molecular sequence data (8) 8
pedigree (8) 8
syndrome (8) 8
zebrafish - embryology (8) 8
adult (7) 7
cell biology (7) 7
genotype & phenotype (7) 7
microcephaly - genetics (7) 7
risk factors (7) 7
signal transduction (7) 7
adolescent (6) 6
amino acid sequence (6) 6
biochemistry & molecular biology (6) 6
diagnosis (6) 6
gene expression (6) 6
genomics (6) 6
infant (6) 6
intellectual disability (6) 6
mental-retardation (6) 6
multidisciplinary sciences (6) 6
physiological aspects (6) 6
abnormalities, multiple - genetics (5) 5
base sequence (5) 5
gene expression regulation, developmental (5) 5
intellectual disability - genetics (5) 5
membrane proteins - genetics (5) 5
young adult (5) 5
zebrafish proteins - genetics (5) 5
abnormalities (4) 4
abnormalities, multiple (4) 4
alleles (4) 4
analysis (4) 4
association (4) 4
biology (4) 4
brain - pathology (4) 4
defects (4) 4
dna (4) 4
embryos (4) 4
exome - genetics (4) 4
gene deletion (4) 4
genetic research (4) 4
health aspects (4) 4
identification and classification (4) 4
medicine (4) 4
mice, inbred c57bl (4) 4
mouse (4) 4
mutation, missense - genetics (4) 4
pediatrics (4) 4
proteins - genetics (4) 4
report (4) 4
rna, messenger - genetics (4) 4
rodents (4) 4
schizophrenia (4) 4
sequence alignment (4) 4
transcription factors - genetics (4) 4
abnormalities, multiple - pathology (3) 3
adaptor proteins, signal transducing - genetics (3) 3
angiogenesis (3) 3
binding sites (3) 3
cell proliferation (3) 3
cells (3) 3
cells, cultured (3) 3
centrosomal protein (3) 3
child development disorders, pervasive - genetics (3) 3
children (3) 3
chromosomes, human, pair 16 - genetics (3) 3
de-novo mutations (3) 3
developmental biology (3) 3
dna copy number variations (3) 3
dna copy number variations - genetics (3) 3
dna-binding proteins - genetics (3) 3
electroporation (3) 3
endothelial-cells (3) 3
exons - genetics (3) 3
expression (3) 3
gene (3) 3
genes, recessive (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatrics, ISSN 0031-4005, 04/2016, Volume 137, Issue 4, pp. 1 - 1
  Autism and autism spectrum disorders represent a group of neurodevelopmental disorders of acute clinical and pathomechanistic heterogeneity. Wong et al... 
Biomarkers | Autism | Mitochondria | Genes
Journal Article
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2014, Volume 111, Issue 42, pp. E4468 - E4477
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2012, Volume 44, Issue 4, pp. 450 - 455
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2009, Volume 41, Issue 3, pp. 359 - 364
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2007, Volume 39, Issue 7, pp. 875 - 881
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2015, Volume 10, Issue 10, pp. e0139614 - e0139614
The endothelial receptor tyrosine kinase (RTK) Tie1 was discovered over 20 years ago, yet its precise function and mode of action remain enigmatic. To shed... 
3-DIMENSIONAL EXTRACELLULAR MATRICES | GROWTH-FACTOR RECEPTOR | LETHALITY | MULTIDISCIPLINARY SCIENCES | ENDOTHELIAL-CELLS | VESSEL DEVELOPMENT | RAC1 | ANGIOPOIETIN-2 | EXPRESSION | RECEPTOR TYROSINE KINASE | VASCULAR MORPHOGENESIS | Human Umbilical Vein Endothelial Cells | Phosphorylation | Humans | Receptor, TIE-1 - metabolism | Zebrafish - embryology | Blood Vessels - embryology | Morphogenesis | Laminin | Angiopoietin-1 - physiology | Proto-Oncogene Proteins c-akt - metabolism | Protein Structure, Tertiary | Mutagenesis, Site-Directed | Proteoglycans | Neovascularization, Physiologic - genetics | Zebrafish Proteins - metabolism | p21-Activated Kinases - metabolism | Phosphothreonine - metabolism | Zebrafish - genetics | Protein Interaction Mapping | Neovascularization, Physiologic - physiology | Animals | Endothelium, Vascular - metabolism | Collagen | Signal Transduction - physiology | Protein Processing, Post-Translational | Enzyme Activation | Drug Combinations | rac1 GTP-Binding Protein - metabolism | Tyrosine | Cells | Endothelium | Pediatrics | Motility | AKT protein | Biology | Activation | Feedback loops | Kinases | Phosphatase | Defects | Proteins | Angiogenesis | Signal transduction | Rodents | Tubes | Protein-tyrosine kinase receptors | Physiology | Cardiology | Protein-tyrosine kinase | Threonine | Blood vessels | p21-activated kinase | Zebrafish | Rac1 protein | Pharmacology | Embryos | Botulinum toxin | Substrates | Endothelial cells | Mode of action | Medicine | Signaling | Ligands | Umbilical vein | Cancer | Guanosinetriphosphatase | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2013, Volume 93, Issue 5, pp. 798 - 811
Journal Article