Synonymer & Information om | Engelska ordet FIBRIL


FIBRIL

1

Antal bokstäver

6

Är palindrom

Nej

9
BR
BRI
FI
FIB
IB
IBR
IL

58

16

152

83
BF
BFI
BI
BIF
BIL


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Exempel på hur man kan använda FIBRIL i en mening

  • Amino acids are bound together to form a triple helix of elongated fibril known as a collagen helix.
  • A myofibril (also known as a muscle fibril or sarcostyle) is a basic rod-like organelle of a muscle cell.
  • In solar physics, a spicule, also known as a fibril or mottle, is a dynamic jet of plasma in the Sun's chromosphere about 300 km in diameter.
  • ECM stiffness was also noted to influence cytoskeletal stiffness, fibronectin fibril assembly, the strength of integrin-cytoskeletal interactions, morphology and motility rate, all of which were known influence cell migration.
  • By taking hexapeptides (six amino acid-long fragments) of a protein of interest and selecting the lowest energy match to a structure similar to that of a known fibril forming hexapeptide, RosettaDesign was able to identify peptides twice as likely to form fibrils as are random proteins.
  • Upon in vitro activation with the pharmacological agent phorbol myristate acetate (PMA), Interleukin 8 (IL-8) or lipopolysaccharide (LPS), neutrophils release granule proteins and chromatin to form an extracellular fibril matrix known as NET through an active process.
  • FACIT collagen (Fibril Associated Collagens with Interrupted Triple helices) is a type of collagen and also a proteoglycan that have two or more triple-helical domains that connect to collagen fibrils and share protein domains with non-collagen matrix molecules.
  • In this case, dermatopontin indicated as domain unfolding of a Fn molecule due to the binding site for anastellin (the only known protein that induce superfibronectin formation) on Fn is located between III_(2-3) and III_(12-14) inside the interaction site, which is the important binding site for the Fn fibril formation.
  • The familial amyloid neuropathies (or familial amyloidotic neuropathies, neuropathic heredofamilial amyloidosis, familial amyloid polyneuropathy) are a rare group of autosomal dominant diseases wherein the autonomic nervous system and/or other nerves are compromised by protein aggregation and/or amyloid fibril formation.
  • The capacity of taxifolin to stimulate fibril formation and promote stabilization of fibrillar forms of collagen can be used in medicine.
  • Mutation in PLOD2 alters the structure of telopeptide lysyl hydroxylase and prevents fibril formation of collagen type 1.
  • Mimiviruses also possess fibril structures on the capsid as well as genes encoding proteins for nucleotide synthesis and various metabolisms that are not found in other viruses.


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