Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains

Genomics

Volumn 83, Issue 6, 2004, Pages 1125-1133

  Marigo, Valeria ^a   Nigro, Alessandra ^a   Pecci, Alessandro ^b   Montanaro, Donatella ^a   Di Stazio, Mariateresa ^a   Balduini, Carlo L ^b   Savoia, Anna ^a  

^a TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^b UNIVERSITY OF PAVIA   (Italy)

Author keywords

Gene expression; MYH10 gene; MYH14 gene; MYH9 gene; MYH9 related disease; Nonmuscle myosin heavy chains II

Indexed keywords

MYOSIN II; MYOSIN IIA; MYOSIN IIB;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DISORDER; AUTOSOMAL DOMINANT INHERITANCE; CELL INCLUSION; CELL LINEAGE; EAR; EMBRYO; EYE; FETUS; GENE EXPRESSION; GRANULOCYTE; KIDNEY; LEUKOCYTE; MEGAKARYOCYTE; MOUSE; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THROMBOCYTOPENIA;

ANIMALS; BONE MARROW; CATARACT; COCHLEA; DEAFNESS; EMBRYO; EYE; GENE EXPRESSION; GRANULOCYTES; HUMANS; IN SITU HYBRIDIZATION; INCLUSION BODIES; KIDNEY; LIVER; MICE; MOLECULAR MOTOR PROTEINS; MYOSIN HEAVY CHAINS; MYOSIN TYPE II; NEPHRITIS; PHENOTYPE; RNA, MESSENGER; SYNDROME; THROMBOCYTOPENIA; TISSUE DISTRIBUTION;

EID: 2642537846     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ygeno.2003.12.012     Document Type: Article

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