itch$41178$ - significado y definición. Qué es itch$41178$
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Qué (quién) es itch$41178$ - definición

PROTEIN-CODING GENE IN THE SPECIES HOMO SAPIENS
ITCH (biology); ITCH (gene)
  • MAPK8 regulates JUNB protein turnover by the phosphorylation of ITCH and a conformational change. Importantly, this regulatory process controls the balance of T helper 2 cytokine production by negatively regulating JUNB turnover and Interleukin 4 transcription.

Grain itch         
SKIN CONDITION CAUSED BY MITES
Barley itch; Mattress itch; Prairie itch; Straw itch; Grain mites; Harvest itch; Cheyletus eruditus; Tyrophagus neiswanderi
Grain itch is a cutaneous condition caused by several types of mites, and characterized by intense pruritus.
Pruritus         
  • [[Swimmer's itch]]
  • [[Scabies]] is one cause of itching.
  • A [[chipmunk]] scratching itself.
  • [[Athlete's foot]] (showing the toes from below plus the front part of the sole)
SENSATION THAT CAUSES THE DESIRE OR REFLEX TO SCRATCH
Itchiness; Itching; Pruritus; Pruritis; Yeuk; Itch cycle; Pruritic; Skin itch; Anogenital pruritus; Generalised pruritus of unknown aetiology; Methylamphetamine-induced pruritus; Puritis; Itches; Chronic pruritus of unknown origin; Itchy skin
·noun Itching.
itching         
  • [[Swimmer's itch]]
  • [[Scabies]] is one cause of itching.
  • A [[chipmunk]] scratching itself.
  • [[Athlete's foot]] (showing the toes from below plus the front part of the sole)
SENSATION THAT CAUSES THE DESIRE OR REFLEX TO SCRATCH
Itchiness; Itching; Pruritus; Pruritis; Yeuk; Itch cycle; Pruritic; Skin itch; Anogenital pruritus; Generalised pruritus of unknown aetiology; Methylamphetamine-induced pruritus; Puritis; Itches; Chronic pruritus of unknown origin; Itchy skin
see itch

Wikipedia

ITCH

ITCH is a HECT domain E3 ubiquitin ligase that is ablated in non-agouti-lethal 18H (aka Itchy) mice. Itchy mice develop a severe immunological phenotype after birth that includes hyperplasia of lymphoid and hematopoietic cells, and stomach and lung inflammation. In humans ITCH deficiency causes altered physical growth, craniofacial morphology defects, defective muscle development, and aberrant immune system function. ITCH contains a C2 domain, proline-rich region, WW domains, HECT domain, and multiple amino acids that are phosphorylated and ubiquitinated.