Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
about
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.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.Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart DiseasesNovel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development.Hypodontia, a prospective predictive marker for tumor?Genetic Disorders of Dental Development: Tales from the Bony Crypt.MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.A novel PITX2 mutation causing iris hypoplasia.MSX1 Modulates RLR-Mediated Innate Antiviral Signaling by Facilitating Assembly of TBK1-Associated Complexes.A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathwayNext generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontiaAdvances in Human Biology: Combining Genetics and Molecular Biophysics to Pave the Way for Personalized Diagnostics and Medicine
P2860
Q34015444-B208089A-7629-4C5C-9100-DFE336AC1BABQ35647855-99A02A03-EF2D-4A44-A66C-9DAB56E07761Q35838050-71226CF8-F485-49E0-941F-89B19A3A1E73Q37472301-60965DC3-C9B8-4AF5-B71C-676C28D27AC7Q38645510-86914FD2-C98E-4840-AFC5-2E55B79928F8Q38765705-E44785C6-FBDE-4D36-973B-B2E45426BD06Q38887068-522DB25B-7992-4447-88DC-C0B52AEB3C3AQ38893835-9798B065-41C8-4D2E-844B-2F69510DBC97Q40668487-B426CE90-C0AE-4447-A8A6-A9AF48133DD9Q58720689-17700A91-6674-4305-8E55-00AC8E94FD0DQ58760165-CA8203DE-DF8F-4D9B-B312-1E12C4C5AFA5Q59042601-F5D1B03C-0DA5-4F7C-BF8B-0CA03FA8BCE3
P2860
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@en
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@nl
type
label
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@en
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@nl
prefLabel
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@en
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@nl
P2093
P2860
P356
P1476
Novel nonsense mutation in MSX ...... n and role of homeodomain/MH4.
@en
P2093
Akio Shibata
Atsuo Nakayama
Hitoshi Miyachi
Junichiro Machida
Kazuo Shimozato
Masashi Kimura
Peter A Jezewski
Seishi Yamaguchi
Tadashi Tatematsu
Yoshihito Tokita
P2860
P356
10.1111/EOS.12105
P577
2013-12-11T00:00:00Z