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2,019 Possible Causes for helix

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  • Influenza

    These studies indicated that an amphipathic helix is found in this region, associated with the inner membrane leaflet.[] -helix and close the channel.[] Note that K235 (blue) and D269 (red) form a salt bridge in ICV HEF that connects helix 230 with loop 270.[]

  • Skin Infection

    A particular localized form known as “chiclero ulcer” affects the helix of one ear and is caused by Leishmania braziliensis or Leishmania mexicana .[]

  • Sunburn

    In the twisting double helix of DNA, four molecules called nucleotides form regular cross-links: Adenosine binds to thymine (AT), and cytosine binds to guanine (CG).[]

  • Dementia

    Johnson, CEO, Global Helix LLC, in Brain Trust magazine, December 2014 issue[]

  • Osteoporosis

    Kulterer et al . [ 64 ] identified the expression of ID4 (encoding inhibitor of DNA binding dominant negative helix-loop-helix protein), CRYAB (alpha-crystallin B chain),[] This may be due to differences in helix formation or cross-linking of collagen, challenging the concept that mineral and matrix composition are normal in osteoporosis and[]

  • Infectious Mononucleosis

    Undeleted strains bound to an undeleted probe migrate low in the gel, while deleted strains migrated high in the gel because of the large malformation of the DNA helix.[] […] homoduplexes) migrate according to size in a polyacrylamide gel, whereas heteroduplexes with base pair differences will migrate more slowly due to malformations in the DNA helix[]

  • Hedera Helix

    Hedera helix subsp. helix , juvenile foliage; Bremerhaven, Germany Hedera helix subsp. helix , adult foliage & flowers; Friedhof St.[] […] f. poetarum Nome [ modifica ] Hedera helix L.[] "RHS Plant Selector - Hedera helix 'Caecilia ' ". Retrieved 21 June 2013. "RHS Plantfinder - Hedera helix 'Ceridwen ' ". Retrieved 2 March 2018.[]

  • Saethre-Chotzen Syndrome

    We have evaluated TWIST, a basic helix-loop-helix transcription factor, as a candidate gene for this condition because its expression pattern and mutant phenotypes in Drosophila[] Abstract Saethre-Chotzen syndrome (ACS III) is an autosomal dominant craniosynostosis syndrome recently ascribed to mutations in the TWIST gene, a basic helix-loop-helix ([] It is caused by mutations in the TWIST gene encoding a basic Helix-Loop-Helix transcription factor.[]

  • Monilethrix

    In these hair keratins, the helix termination motif, HTM, was the only site in which mutations were located.[] The gene segment encoding the helix termination motif region of keratin hHb6 was PCR amplified and sequenced. Mutations were recognized in 6 families.[] […] mutations in the type II hair cortex keratins hHb6 and hHb1 were restricted to a highly conserved glutamic acid residue Glu413 (Glu117 of the 2B subdomains) in the EIATYRRLLEGEE helix[]

  • Pitt-Hopkins Syndrome

    These findings demonstrate that TCF4 anomalies are responsible for PHS and provide the first evidence of a human disorder related to class I basic helix-loop-helix transcription-factor[] TCF4 encodes a basic helix-loop-helix transcription factor that interacts with other transcription factors to activate or repress gene expression.[] Breakpoint-mapping by fluorescence in situ hybridization indicated that on chromosome 18, the basic helix-loop-helix transcription factor TCF4 gene is disrupted by the breakpoint[]

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