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myh9-related disease (94) 94
humans (86) 86
index medicus (70) 70
myosin heavy chains - genetics (60) 60
molecular motor proteins - genetics (56) 56
thrombocytopenia - genetics (55) 55
hematology (51) 51
female (47) 47
male (46) 46
mutation (42) 42
adult (39) 39
mutations (31) 31
myosin (29) 29
expression (26) 26
leukocyte inclusions (26) 26
thrombocytopenia (26) 26
macrothrombocytopenia (25) 25
animals (24) 24
myosin heavy-chain (24) 24
thrombocytopenia - congenital (24) 24
adolescent (23) 23
child (22) 22
hearing loss, sensorineural - genetics (22) 22
phenotype (22) 22
fechtner-syndrome (21) 21
muscle proteins (21) 21
myh9 (21) 21
middle aged (20) 20
child, preschool (19) 19
thrombocytopenia - diagnosis (19) 19
autosomal-dominant macrothrombocytopenia (18) 18
deafness (18) 18
epstein (18) 18
thrombocytopenia - pathology (18) 18
disorders (16) 16
peripheral vascular disease (16) 16
genetics & heredity (15) 15
myosin heavy chains - metabolism (15) 15
young adult (15) 15
blood platelets - pathology (14) 14
epstein-syndrome (14) 14
genetic aspects (14) 14
inherited thrombocytopenia (14) 14
nonmuscle myosin type iia - genetics (14) 14
pedigree (14) 14
myh9 gene (13) 13
thrombocytopenia - blood (13) 13
dna mutational analysis (12) 12
exons (12) 12
fechtner (12) 12
iia (12) 12
mice (12) 12
molecular motor proteins - metabolism (12) 12
proplatelet formation (12) 12
heavy-chain iia (11) 11
myh9 mutations (11) 11
platelets (11) 11
syndrome (11) 11
urology & nephrology (11) 11
cataract - genetics (10) 10
gene (10) 10
genetic disorders (10) 10
cell biology (9) 9
genetic predisposition to disease (9) 9
molecular motor proteins - chemistry (9) 9
mutation, missense (9) 9
myosin heavy chains - chemistry (9) 9
nonmuscle myosin type iia - metabolism (9) 9
thrombocytopenia - physiopathology (9) 9
aged (8) 8
article (8) 8
bernard-soulier-syndrome (8) 8
blood platelets - metabolism (8) 8
deafness - genetics (8) 8
diagnosis, differential (8) 8
inherited thrombocytopenias (8) 8
localization (8) 8
medicine (8) 8
medicine & public health (8) 8
mutation - genetics (8) 8
myh9-related disorders (8) 8
oncology (8) 8
patient (8) 8
platelet count (8) 8
point mutation (8) 8
diagnosis (7) 7
epstein syndrome (7) 7
genotype (7) 7
identification (7) 7
may-hegglin (7) 7
may-hegglin anomaly (7) 7
pediatrics (7) 7
thrombocytopenia - complications (7) 7
analysis (6) 6
base sequence (6) 6
biochemistry & molecular biology (6) 6
cell line (6) 6
fechtner syndrome (6) 6
fechtner syndromes (6) 6
fluorescent antibody technique (6) 6
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Human Mutation, ISSN 1059-7794, 02/2014, Volume 35, Issue 2, pp. 236 - 247
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 04/2010, Volume 103, Issue 4, pp. 826 - 832
Journal Article
Gene, ISSN 0378-1119, 07/2018, Volume 664, pp. 152 - 167
The gene encodes the heavy chain of non-muscle myosin IIA, a widely expressed cytoplasmic myosin that participates in a variety of processes requiring the... 
Kidney disease | Actin-myosin cytoskeleton | Deafness | Inherited thrombocytopenia | Class II myosin | Mouse models | Cell-cell adhesion | Non-muscle myosin | MYH9-related disease | Tumor suppressor | MYH9 gene | PROTEIN-KINASE-C | INHERITED THROMBOCYTOPENIAS | GENOTYPE-PHENOTYPE CORRELATIONS | HEAVY-CHAIN IIA | PLATELET MYOSIN | SMOOTH-MUSCLE MYOSIN | GENETICS & HEREDITY | MAY-HEGGLIN | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | FECHTNER-SYNDROME | Myosin Heavy Chains - chemistry | Cell Line | Phosphorylation | Deafness - genetics | Humans | Thrombocytopenia - congenital | Myosin Heavy Chains - genetics | Hearing Loss, Sensorineural - genetics | Molecular Motor Proteins - chemistry | Molecular Motor Proteins - genetics | Myosin Heavy Chains - metabolism | Nonmuscle Myosin Type IIA - metabolism | Thrombocytopenia - genetics | Animals | Neoplasms - genetics | Nonmuscle Myosin Type IIA - genetics | Renal Insufficiency, Chronic - genetics | Molecular Motor Proteins - metabolism | Mice | Mutation | Nonmuscle Myosin Type IIA - chemistry | Embryonic development | Squamous cell carcinoma | Fluorescence | Transforming growth factors | Embryonic stem cells | Muscle proteins | Chronic kidney failure | Casein | Actin | Analysis | Myosin | Protein kinases | Protein binding | mouse models | cell-cell adhesion | inherited thrombocytopenia | actin-myosin cytoskeleton | kidney disease | tumor suppressor | class II myosin | non-muscle myosin | deafness
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e67839
Journal Article
Indian Journal of Otology, ISSN 0971-7749, 10/2018, Volume 24, Issue 4, pp. 270 - 273
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2012, Volume 56, Issue 1, pp. 7 - 12
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 09/2018, Volume 16, Issue 9, pp. 1700 - 1710
Journal Article