The intracellular threonine of amyloid precursor protein that is essential for docking of Pin1 is dispensable for developmental function

PLoS ONE

Volumn 6, Issue 3, 2011, Pages

  Barbagallo, Alessia P M ^a   Wang, Zilai ^b   Zheng, Hui ^b   D'Adamio, Luciano ^a,c  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; AMYLOID PRECURSOR LIKE PROTEIN 2; AMYLOID PRECURSOR PROTEIN; GENE PRODUCT; PEPTIDYLPROLYL ISOMERASE PIN1; PROTEIN MINT1; THREONINE; UNCLASSIFIED DRUG; NIMA INTERACTING PEPTIDYLPROLYL ISOMERASE; NIMA-INTERACTING PEPTIDYLPROLYL ISOMERASE; PEPTIDYLPROLYL ISOMERASE;

AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; LETHALITY; MOLECULAR DOCKING; MOUSE; NEUROMUSCULAR JUNCTION DISORDER; NONHUMAN; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; SYNAPTOGENESIS; ANIMAL; C57BL MOUSE; FLUORESCENT ANTIBODY TECHNIQUE; METABOLISM;

MUS;

AMYLOID BETA-PROTEIN PRECURSOR; ANIMALS; FLUORESCENT ANTIBODY TECHNIQUE; MICE; MICE, INBRED C57BL; PEPTIDYLPROLYL ISOMERASE; THREONINE;

EID: 79952952445     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0018006     Document Type: Article

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