about
Purification and molecular cloning of a secreted, Frizzled-related antagonist of Wnt actionMutations in WNT1 cause different forms of bone fragilityThe transcription factor Zfp423/OAZ is required for cerebellar development and CNS midline patterning.Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequencesThe Engrailed homeobox genes determine the different foliation patterns in the vermis and hemispheres of the mammalian cerebellum.Wnt family proteins are secreted and associated with the cell surfaceThe WntsHeparan sulfate proteoglycans: a sugar code for vertebrate development?The role of the ubiquitin proteasome system in cerebellar development and medulloblastomaβ-Catenin is critical for cerebellar foliation and laminationThe ups and downs of Wnt signaling in prevalent neurological disordersRostral cerebellar malformation (rcm/rcm): a murine mutant to study regionalization of the cerebellumWNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta.A quantitative survey of gravity receptor function in mutant mouse strains.Genetic dissection of midbrain dopamine neuron development in vivo.Clinical nosologic and genetic aspects of Joubert and related syndromes.Zebrafish E-cadherin: expression during early embryogenesis and regulation during brain development.The role of thioredoxin reductases in brain development.Neurogenetics of the cerebellar system.The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutationsHomozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneityNeural plate patterning: upstream and downstream of the isthmic organizer.Three decades of Wnts: a personal perspective on how a scientific field developed.Novel receptor protein tyrosine phosphatase (RPTPrho) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortex.Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome.WNT3 inhibits cerebellar granule neuron progenitor proliferation and medulloblastoma formation via MAPK activation.Phenotypes in mTERT⁺/⁻ and mTERT⁻/⁻ mice are due to short telomeres, not telomere-independent functions of telomerase reverse transcriptaseRelevance of Wnt signaling for osteoanabolic therapy.WNTs in the vertebrate nervous system: from patterning to neuronal connectivity.Genetic basis of Joubert syndrome and related disorders of cerebellar development.Expression of Wnt-1 in PC12 cells results in modulation of plakoglobin and E-cadherin and increased cellular adhesionDynamic temporal requirement of Wnt1 in midbrain dopamine neuron development.Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutationsCancer stem cells and brain tumors: uprooting the bad seeds.Wnt signaling in vertebrate neural development and function.Epigenetic Interactions and Gene Expression in Peri-Implantation Mouse Embryo DevelopmentEstablishing diversity in the dopaminergic system.Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasisNeurodevelopmental Perspectives on Wnt Signaling in Psychiatry.Temporal Expression of Wnt1 Defines the Competency State and Terminal Identity of Progenitors in the Developing Cochlear Nucleus and Inferior Colliculus
P2860
Q24311356-2A564A66-39F9-4127-A049-F607016F3E5BQ24336287-A5D92DB5-C249-4FFD-B826-682984B73F73Q24624584-BC0B2024-B527-476E-A9B0-C96522706EB4Q24629091-3BE7733F-B86E-4D83-873E-32F8D598F297Q24633285-3588657D-C142-4119-BCC4-7C70CF176DE3Q24656977-94B64C4F-92D2-4B06-8C7B-9C9FAD7D2EB2Q24802301-78131B17-A2A5-4929-964D-D9E945C5FBE2Q26781120-0AACB813-01D7-4C32-A0AB-93C193034541Q26782159-7DAEE4AE-3DB1-4CA3-A6D7-2DDDC095F41DQ27318680-5088D66B-BAAC-4DB6-8ACB-13E085EDC5BEQ28277009-70F72D94-D9D2-45A7-B3DA-9216BC74948CQ28511321-32CACD7E-AE9B-4D96-B406-A6C52A9398EBQ30448491-0D9FC861-A1EB-425C-8BD2-2F06945968ABQ30492589-9FDAA35A-9034-4DA7-9F2A-0E1C798B36D8Q30528530-62E7C8A7-20F2-4DFA-8DBF-2CF9BBAF438BQ30582278-1988FB79-EE67-4E6A-AFD4-2C8407662DDEQ30990622-2249F538-D379-41D9-A7D8-46C9BFF28234Q33324392-1FE29676-BDCF-44F1-866F-31A77E7B1CE1Q33733717-E96B267A-8D8E-4619-8777-BA3A29675A97Q33847609-7D24219C-56C9-43B3-81EB-A54B926FEAFEQ34146365-2402C173-1D33-4681-9671-B6B594235C93Q34185965-E0ED0CDC-7914-4814-A5A1-C09107E5823EQ34276643-F570BD97-E701-4F51-BBEC-18CFC50C85FBQ34458651-42B7CF43-8440-4975-9EAD-9A31B4257275Q35032831-7A9192D6-3E5A-4909-8140-CC9D1C323D1BQ35058659-BBFC6D08-1554-40F0-B1E4-7CB46DDD1F2BQ35096706-6691B814-E94B-412F-9781-6C6C3ECBBA9BQ35673905-844A01A0-51FD-4159-AB9C-14089B2405C5Q36098890-71DE63DD-99D0-4CDF-B096-32CF6FE7EEFBQ36294694-433FB67E-D1DF-4363-BBE1-C24EA58790FBQ36534670-8278470E-4EFC-4419-8835-A39DE8A45B0BQ36648669-7528CF05-0EDC-4D4A-8197-5B5143F31DADQ36983068-6985A850-7FD1-44F7-A3C3-A27DFD17A2DCQ37004676-F4744465-D26E-4EF5-83DB-43DF7291B16EQ38046770-E0A77622-D0D8-4254-AC04-87C3AA076EC9Q38263810-54A10FBC-4A7F-4059-9552-33F4487D47FBQ38598047-91BA7EC9-B159-4E0B-A463-B2AD9C039395Q38719412-72E41EA5-93F2-4816-B62C-59EEE4CE5098Q38917986-B19BB469-E9FB-4801-96FC-9636E5108A47Q41525645-B6B8BB59-0856-453F-8C9A-BB2E67A3695C
P2860
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh-hant
name
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@en
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@nl
type
label
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@en
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@nl
prefLabel
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@en
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@nl
P2093
P1433
P1476
Swaying is a mutant allele of the proto-oncogene Wnt-1.
@en
P2093
P304
P356
10.1016/0092-8674(91)90369-A
P407
P577
1991-11-01T00:00:00Z