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Piezos are large transmembrane proteins conserved among various species, all having between 24 and 36 predicted transmembrane domains. Additionally we are shipping Family with Sequence Similarity 38, Member B Antibodies (57) and many more products for this protein.
we report the developmental phenotypic spectrum of familial Gordon syndrome in one family due to the previously characterized PIEZO2 mutation c.8057G>A.
Enterochromaffin cells in the human and mouse small bowel GI epithelium selectively express the mechanosensitive ion channel Piezo2, and also that activation of Piezo2 by force leads to inward currents, 5-HT (show DDC ELISA Kits) release and an increase in mucosal secretion
The Piezo2 convert a variety of mechanical stimuli into channel activation and subsequent inactivation, and what molecules and mechanisms modulate Piezo function.
we report a consanguineous family with three siblings who showed short stature, scoliosis, gross motor impairment, and a progressive form of contractures involving the distal joints that is distinct from that found in patients with domina Recessive mutations in PIEZO2 thus appear to cause a progressive phenotype that overlaps with, while being mostly distinct from that associated with dominant mutations in the same gene
Sensory ataxia and proprioception defect with dorsal column involvement together with arthrogryposis, myopathy, scoliosis and progressive respiratory failure may represent a distinct clinical phenotype, and indicate recessive mutations in PIEZO2
We identified homozygous loss of function variants in PIEZO2 as the underlying cause for an autosomal-recessive distal muscular atrophy with arthrogryposis, kyphoscoliosis, and neonatal respiratory insufficiency distinct from previously described dominant PIEZO2 diseases.
Our results show that PIEZO2 is a determinant of mechanosensation in humans.
Transgenic mouse lines lacking Piezo2 in proprioceptive neurons showed severely uncoordinated body movements.
Whole-exome sequencing revealed a novel heterozygous mutation c.4456G>C (p.A1486P) of PIEZO2.
family of mechanically activated channels that counts only two members in human, piezo1 (show PIEZO1 ELISA Kits) and 2, has emerged recently. [review]
experiments demonstrate a role for Pericentrin (show PCNT ELISA Kits) in modulating Piezo2 activity and membrane expression in somatosensory neurons
Piezo2 is an airway stretch sensor; Piezo2-mediated mechanotransduction within various airway-innervating sensory neurons is critical for establishing efficient respiration at birth and maintaining normal breathing in adult mice
Astrocytes in optic nerve head express multiple mechanosensitive channels, in particular Piezo1 (show PIEZO1 ELISA Kits) and 2. The expression of putative mechanosensitive channels in these cells may contribute to their responsiveness to traumatic or glaucomatous injury.
mice lacking Piezo2 in both adult sensory neurons and Merkel cells exhibit a profound loss of touch sensation
engineered mice deficient in Piezo2 in the skin, but not in sensory neurons, show that Merkel-cell mechanosensitivity completely depends on Piezo2
data indicate that the Epac1 (show RAPGEF3 ELISA Kits)-Piezo2 axis has a role in the development of mechanical allodynia during neuropathic pain
piezo2 sensitization may contribute to PKA- and PKC-mediated mechanical hyperalgesia.
overexpression of Piezo1 (show PIEZO1 ELISA Kits) or Piezo2 induced 2 kinetically distinct mechanically activated (MA) currents; Piezos are expressed in several tissues; propose that Piezos are components of MA cation channels
Piezos are large transmembrane proteins conserved among various species, all having between 24 and 36 predicted transmembrane domains. 'Piezo' comes from the Greek 'piesi,' meaning 'pressure.' The PIEZO2 protein has a role in rapidly adapting mechanically activated (MA) currents in somatosensory neurons (Coste et al., 2010
family with sequence similarity 38, member B
, family with sequence similarity 38, member B2
, protein PIEZO2