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Notes in
Tissue architecture
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charlie-robert-fillet-august-march-six
Status
Last Update
Fields
Published
09/23/2024
{{c1::F-actin}} is made up of {{c2::G-actin monomers}}
Published
09/23/2024
{{c1::actin}} is a {{c2::microfilament}}
Published
09/23/2024
{{c1::actin}} is essential for cell {{c2::movements}}
Published
09/23/2024
{{c1::Phalloidin}} binds and {{c3::stabilizes}} {{c2::actin}} filaments
Published
09/23/2024
{{c1::Cytochalasin}} caps filament {{c2::plus end}}, preventing polymerization there
Published
09/23/2024
{{c1::Latrunculin}} binds to {{c2::g-actin monomers}} and prevents their polymerization
Published
09/23/2024
{{c1::Mictrotubles}} are made up of {{c2::alpha and beta tubulin}}
Published
09/23/2024
{{c1::Microtubles}} play a large role in {{c5::{{c2::cell organization}}, {{c3::transport within a cell}}, and {{c4::cillia}}}}
Published
09/23/2024
{{c1::microtubles}} can rapidly under {{c2::assembly and disassembly}}
Published
09/23/2024
{{c1::Taxol}} binds and {{c2::stabilizes microtubles}} {{c3::preventing}} depolermization
Published
09/23/2024
{{c1::{{c3::Colchicine/colcemid}} and {{c4::Vinblastine/vincristine}}}} binds {{c2::tubulin dimers}} and prevents their polymerization
Published
09/23/2024
{{c1::Intermediate filaments}} have a high {{c2::tensile strength}}
Published
09/23/2024
The {{c1::nuclear lamina}} is formed of {{c2::intermediate filaments}}
Published
09/23/2024
{{c1::Hutchinson-Gilford Progeria Syndrome (HGPS)}} is a defect in the {{c2::nuclear lamina}} and presents as {{c3::premature aging}}
Published
09/23/2024
The {{c1::cytoskeletal filamanets}} are {{c2::microfilaments, microtubules, and intermediate filaments}}
Published
09/23/2024
{{c1::Extracellular matrix}} are made up of {{c2::proteoglycans, collagens, and multi-adhesive matrix proteins}}
Published
09/23/2024
{{c3::Collagen}} has 2 types {{c1::fibrillar}} and {{c2::nonfibrillar}}
Published
09/23/2024
{{c1::collagen}} forms a {{c2::triple helical}} structures
Published
09/23/2024
Every third amino acid in {{c1::collagen}} is {{c2::glysine}}
Published
09/23/2024
{{c1::Osteogenesis imperfecta}} is a AA mutations for {{c2::glycine}} which misfolds {{c3::collagen}}
Published
09/23/2024
{{c1::Goodpasture syndrome}} is a {{c2::type IV collagen}} mutation
Published
09/23/2024
Non collagenous proteins in the Extra cellular matrix are {{c1::{{c2::elastin}}, {{c3::fibronectin}}, and {{c4::laminin}}}}
Published
09/23/2024
{{c1::Laminin}} is defective in {{c2::muscular dystrophy}}
Published
09/23/2024
{{c1::Proteoglycans}} are core proteins with {{c2::glycosaminoglycans (GAGs)}}
Published
09/23/2024
{{c1::Proteoglycans}} form the {{c2::"ground substance"}}
Published
09/23/2024
The triple helix of collagen starts to wind at the {{c1::C}} terminal propeptide
Published
09/23/2024
If there is no {{c1::vitamin C}} then {{c2::prolyl hydroxylase}} cannot hydroxylize proline
Published
09/23/2024
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09/23/2024
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09/23/2024
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09/23/2024
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09/23/2024
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09/23/2024
{{c1::Cell adhesion molecules}} are {{c2::cadherins, integrins, selectins, Ig-superfamily}}
Published
09/23/2024
{{c1::Cadherins}} do {{c2::cell to cell}} adhesion
Published
09/23/2024
{{c1::Integrins}} do {{c2::Cell-ECM/Cell-Cell}} adhesion
Published
09/23/2024
{{c1::Selectins}} do {{c2::Cell-Cell (in the circulatory system)}} adhesion
Published
09/23/2024
{{c1::Ig-superfamily}} does {{c2::all varieties}} of adhesion
Status
Last Update
Fields