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Assessing the Impact of Drought Stress on Hemp (Cannabis sativa L.) Fibers. [PDF]
Materials (Basel)Kwiatkowska E +4 more
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Barns rett til å bli hørt : ved omsorgsovertakelse
, 2007 Marianne Aasland Gisholt
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Characterization of adenosinergic system in Rett syndrome
, 2015 Catarina Miranda Lourenço
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Current Opinion in Genetics & Development, 1996
RET mutations have been identified as the underlying cause of two congenital diseases that predominately affect tissues of neural crest origin: the MEN 2 cancer syndromes and a proportion of cases of dominantly inherited Hirschsprung disease, a disorder of gut development.
Y F, Mak, B A, Ponder
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RET mutations have been identified as the underlying cause of two congenital diseases that predominately affect tissues of neural crest origin: the MEN 2 cancer syndromes and a proportion of cases of dominantly inherited Hirschsprung disease, a disorder of gut development.
Y F, Mak, B A, Ponder
openaire +2 more sources
2006
The human RET (REarranged during transfection) gene maps on chromosome 10q11.2 and codes for a single pass transmembrane protein.The intracellular portion features a typical tyrosine kinase domain.RET is expressed primarily in peripheral enteric, sympathetic and sensory neurons, and in central motor, dopaminergic and noradrenergic neurons.
VECCHIO, GIANCARLO +2 more
openaire +3 more sources
The human RET (REarranged during transfection) gene maps on chromosome 10q11.2 and codes for a single pass transmembrane protein.The intracellular portion features a typical tyrosine kinase domain.RET is expressed primarily in peripheral enteric, sympathetic and sensory neurons, and in central motor, dopaminergic and noradrenergic neurons.
VECCHIO, GIANCARLO +2 more
openaire +3 more sources