Myosin MyTH4-FERM structures highlight important principles of convergent evolution.

scientific article published on 10 May 2016

Myosin MyTH4-FERM structures highlight important principles of convergent evolution. is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2016PNAS..113E2906P
P356DOI10.1073/PNAS.1600736113
P932PMC publication ID4889382
P698PubMed publication ID27166421

P50authorAnne Houdusse-JuilléQ15845472
Vicente J Planelles-HerreroQ88413689
Florian BlancQ88909943
Yannick SouriguesQ125267352
Margaret A TitusQ125267385
Helena SirkiaQ125267431
Jeffrey ClauseQ125267485
Serena SiriguQ125267514
Marco CecchiniQ50633765
P2093author name stringSusan P Gilbert
Beatrice Amigues
Daniel O Johnsrud
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P433issue21
P407language of work or nameEnglishQ1860
P921main subjectconvergent evolutionQ200312
P304page(s)E2906-15
P577publication date2016-05-10
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleMyosin MyTH4-FERM structures highlight important principles of convergent evolution
P478volume113

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cites work (P2860)
Q41048804Kinetic adaptation of human Myo19 for active mitochondrial transport to growing filopodia tips
Q37515120MyTH4-FERM myosins have an ancient and conserved role in filopod formation
Q39005661MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions
Q40984886Myosin 7 and its adaptors link cadherins to actin.
Q47139973Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation.
Q38683544Novel functions of CCM1 delimit the relationship of PTB/PH domains.
Q90702016Optimized filopodia formation requires myosin tail domain cooperation
Q41047666ROS induced distribution of mitochondria to filopodia by Myo19 depends on a class specific tryptophan in the motor domain.
Q43058873Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins.
Q52670923The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families.

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