Division of Perinatology,
Institute for Developmental Research,
Division of Perinatology, Institute for Developmental Research
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Phosphorylation of neuroglycan C, a brain-specific transmembrane chondroitin sulfate proteoglycan, and its localization in the lipid rafts.
The Journal of biological chemistry Jun, 2002 | Pubmed ID: 11929867
Developmental changes in the biochemical and immunological characters of the carbohydrate moiety of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan.
Glycoconjugate journal , 2004 | Pubmed ID: 15115911
Glycosylation site for chondroitin sulfate on the neural part-time proteoglycan, neuroglycan C.
The Journal of biological chemistry Nov, 2004 | Pubmed ID: 15331613
Neuroglycan C, a brain-specific part-time proteoglycan, with a particular multidomain structure.
Glycoconjugate journal , 2004 | Pubmed ID: 15467399
Changes in the amounts of chondroitin sulfate proteoglycans in rat brain after neonatal hypoxia-ischemia.
Journal of neuroscience research Sep, 2005 | Pubmed ID: 16041802
Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region.
Human mutation Jan, 2006 | Pubmed ID: 16281288
Expression and identification of a new splice variant of neuroglycan C, a transmembrane chondroitin sulfate proteoglycan, in the human brain.
Journal of neuroscience research Jan, 2006 | Pubmed ID: 16299773
Identification and functions of chondroitin sulfate in the milieu of neural stem cells.
The Journal of biological chemistry Mar, 2006 | Pubmed ID: 16373347
Identification of neurite outgrowth-promoting domains of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan, and involvement of phosphatidylinositol 3-kinase and protein kinase C signaling pathways in neuritogenesis.
The Journal of biological chemistry Aug, 2006 | Pubmed ID: 16803884
Ectodomain shedding of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan, by TIMP-2- and TIMP-3-sensitive proteolysis.
Journal of neurochemistry Sep, 2007 | Pubmed ID: 17532789
A highly sulfated chondroitin sulfate preparation, CS-E, prevents excitatory amino acid-induced neuronal cell death.
Journal of neurochemistry Mar, 2008 | Pubmed ID: 17996021
Reduction of brain injury in neonatal hypoxic-ischemic rats by intracerebroventricular injection of neural stem/progenitor cells together with chondroitinase ABC.
Reproductive sciences (Thousand Oaks, Calif.) Jul, 2008 | Pubmed ID: 18579850
Neuroglycan C, a brain-specific chondroitin sulfate proteoglycan, interacts with pleiotrophin, a heparin-binding growth factor.
Neurochemical research Aug, 2010 | Pubmed ID: 20369290
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.
European journal of human genetics : EJHG Aug, 2011 | Pubmed ID: 21448236
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
European journal of oral sciences Feb, 2014 | Pubmed ID: 24329876
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.
PloS one , 2014 | Pubmed ID: 25101640
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.
PloS one , 2015 | Pubmed ID: 26030286
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.
Mutagenesis Jan, 2016 | Pubmed ID: 26220009
A novel PITX2 mutation causing iris hypoplasia.
Human genome variation , 2014 | Pubmed ID: 27081499
Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23.
Brain & development Feb, 2017 | Pubmed ID: 27692871
Identification of Nuclear Localization Signals in the Human Homeoprotein, MSX1.
Biochemistry and cell biology = Biochimie et biologie cellulaire Nov, 2017 | Pubmed ID: 29156143
WNT10A variants isolated from Japanese patients with congenital tooth agenesis.
Human genome variation , 2017 | Pubmed ID: 29367877
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