Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
about
Opposing roles for JNK and Aurora A in regulating the association of WDR62 with spindle microtubules.A novel single base pair duplication in WDR62 causes primary microcephaly.Molecular genetics of human primary microcephaly: an overview.Asymmetric cell division of granule neuron progenitors in the external granule layer of the mouse cerebellum.Aurora A phosphorylation of WD40-repeat protein 62 in mitotic spindle regulation.Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.Novel mutations c.28G>T (p.Ala10Ser) and c.189G>T (p.Glu63Asp) in WDR62 associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly type 2.Molecular and cellular basis of autosomal recessive primary microcephaly.WDR62 overexpression is associated with a poor prognosis in patients with lung adenocarcinoma.The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development.A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.Nek5: a new regulator of centrosome integrity.
P2860
Q35029169-6F840782-886F-4917-8FFA-8BD845871BE7Q35321786-2DA436EE-4382-44A4-9CC1-957DAB0117A0Q35624539-63512E38-1016-40BF-9431-E14277D87377Q36063074-2E431E87-39A9-45D5-B33E-34F9BC06683DQ37091944-FD336364-CA43-4120-AA0F-29F90732E03EQ37685924-BC0E2F93-01EA-4168-ACAA-FA0BDE4266B1Q37694637-67C92885-76FC-4B06-A2C4-994CE7B00BBAQ38303675-B8B1860E-46AE-43ED-85CE-4FED8A0EBD6DQ38712957-029E0278-17E0-40B3-B538-6B68031B5374Q41918329-5AFD33DB-F9E9-457C-9B0D-3C3638D8C2E0Q41920199-E3C41E27-8949-46E7-A784-FEF4B24AC746Q43112506-601BDA33-F07A-40DE-B813-168849AD5BCF
P2860
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@ast
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@en
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@nl
type
label
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@ast
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@en
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@nl
prefLabel
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@ast
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@en
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@nl
P2093
P2860
P921
P356
P1476
Abnormal centrosome and spindl ...... terozygous WDR62 gene mutation
@en
P2093
Angela Huebner
Detlev Schindler
Ethiraj Ravindran
Heba Gamal Farag
Nadine Kraemer
Sebastian Froehler
Timo Staab
P2860
P2888
P356
10.1186/1750-1172-8-178
P577
2013-11-14T00:00:00Z
P5875
P6179
1050879935