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Nature (London), ISSN 1476-4687, 2010, Volume 464, Issue 7290, pp. 917 - 921
The vascular endothelial growth factors (VEGFs) are major angiogenic regulators and are involved in several aspects of endothelial cell physiology(1). However,... 
TRANSPORT | LACKING | LIPID-METABOLISM | ANGIOGENESIS | PERMEABILITY | LETHALITY | MULTIDISCIPLINARY SCIENCES | MOUSE | FLT-1 | VEGF-B | RECEPTOR-1 | Neuropilin-1 - genetics | Vascular Endothelial Growth Factor B - deficiency | Oligonucleotide Array Sequence Analysis | Neuropilin-1 - metabolism | Humans | Adipose Tissue, White - metabolism | Male | Mitochondrial Proteins - genetics | Biological Transport | Mitochondria - genetics | Mitochondrial Proteins - metabolism | Myocardium - metabolism | Transcription, Genetic | Muscles - metabolism | Fatty Acids - metabolism | Cell Line | Signal Transduction | Mice, Inbred C57BL | Cells, Cultured | Gene Expression Regulation | Vascular Endothelial Growth Factor Receptor-1 - metabolism | Mitochondria - metabolism | Organ Specificity | Endothelium - cytology | Animals | Cell Nucleus - genetics | Endothelium - metabolism | Vascular Endothelial Growth Factor B - metabolism | Vascular Endothelial Growth Factor B - genetics | Adipose Tissue, Brown - metabolism | Mice | Fatty Acid Transport Proteins - genetics | Care and treatment | Physiological aspects | Genetic aspects | Diabetes | Research | Cardiovascular diseases | Vascular endothelial growth factor | Proteins | Signal transduction | Rodents | Binding sites | Genetik | Biokemi och molekylärbiologi | Cell and Molecular Biology | Biochemistry and Molecular Biology | Genetics | Cellbiologi | Cell- och molekylärbiologi | Cell Biology
Journal Article
BMC research notes, ISSN 1756-0500, 2011, Volume 4, Issue 1, pp. 90 - 90
...Authors: Maria Sobol [1,2]; Niklas Dahl [1]; Joakim Klar (corresponding author) [1] Introduction Ichthyosis prematurity syndrome (IPS) is a rare form... 
Gene mutations | Carrier proteins | Physiological aspects | Genetic aspects | Research | Health aspects | Risk factors | Ichthyosis | Proteins | Genotype & phenotype | Premature birth | Genetics | Mutation | Family medical history | Genetic testing | Manuscripts | Siblings
Journal Article
PLoS genetics, ISSN 1553-7404, 2017, Volume 13, Issue 7, p. e1006897
Journal Article
European journal of human genetics : EJHG, ISSN 1476-5438, 2017, Volume 25, Issue 7, pp. 848 - 853
Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 2014, Volume 124, Issue 11, pp. 4773 - 4780
Journal Article
BMC medical genetics, ISSN 1471-2350, 12/2012, Volume 13, Issue 1, pp. 120 - 120
Journal Article
Neurobiology of disease, ISSN 0969-9961, 2019, Volume 132, p. 104583
Dravet syndrome (DS) is an early onset refractory epilepsy typically caused by de novo heterozygous variants in SCN1A encoding the α-subunit of the neuronal... 
Chromatin architecture | Neural differentiation | Nav1.1 | Dravet syndrome | iPSC | Neurodevelopment | SCN1A | Na(v)1.1 | S-TRANSFERASE M1 | CORTICAL INTERNEURONS | STEM-CELLS | NEUROSCIENCES | HAPLOINSUFFICIENCY | ENCEPHALOPATHY | MOUSE MODEL | EPIGENETIC REGULATION | GENE-EXPRESSION | SEVERE MYOCLONIC EPILEPSY | DENTATE GYRUS
Journal Article