Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.
about
Linkage between the mechanisms of thrombocytopenia and thrombopoiesisMolecular mechanisms of disease-causing missense mutationsEstablishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines.MYH-9 Related Platelet Disorders: Strategies for Management and DiagnosisAlteration of liver enzymes is a feature of the MYH9-related disease syndrome.MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlationsCochlear implantation is safe and effective in patients with MYH9-related disease.Prediction of disease-related mutations affecting protein localization.Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders.Perinatal Management for a Pregnant Woman with an MYH9 Disorder.Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings of MYH9-Related Disease.Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA.
P2860
Q26770863-0926D907-E9C7-40B5-9983-559C899CDB25Q27021940-6AF91B79-84C6-4E9A-8F43-E0C8CF75831DQ31127014-8DFC3756-3B87-427E-9DF6-B2278B133265Q33382216-0177B070-8DD4-42F7-877B-E657B5245EE2Q33393007-AC7C800C-28D0-48D1-A6C4-C3059BB00423Q33401062-CEA03A93-7967-411A-A8CF-D4EF1AE8DF4BQ33404204-CFAF7D02-7CAC-4A10-B111-8B04A087040DQ33416191-B446E945-9AB3-408B-B00C-B78D4C22B0F4Q33421104-E6DDA905-9059-49E5-BFE1-193435744371Q33960799-D64C1594-8B54-458D-B45A-73F79FDEF7EBQ37089075-41038FE4-D789-4D14-A7FF-DE8819AE95D0Q38879947-EAA55AE4-F0D5-4A6F-A6FC-6DB019CE4EC6Q42550917-1E4B28BA-6FAD-4222-A30E-AECFE132EFFC
P2860
Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@ast
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@en
type
label
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@ast
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@en
prefLabel
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@ast
Immunofluorescence analysis of ...... alization with MYH9 mutations.
@en
P2093
P1476
Immunofluorescence analysis of ...... calization with MYH9 mutations
@en
P2093
Chikako Inoue
Eun-Kyeong Jo
Fumihiro Kimura
Hidehiko Saito
Masahiro Sako
Shinji Kunishima
Tadashi Kamiya
Tadashi Matsushita
Tetsuhito Kojima
P304
P356
10.1097/01.LAB.0000050960.48774.17
P577
2003-01-01T00:00:00Z
P6179
1013058971