RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
about
Function Over Form: Modeling Groups of Inherited Neurological Conditions in ZebrafishUnraveling molecular pathways shared by Kabuki and Kabuki-like syndromes.Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome.Zebrafish models of cardiovascular disease.Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency.Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2.Congenital heart defects in molecularly proven Kabuki syndrome patients.Interrupted/bipartite clavicle as a diagnostic clue in Kabuki syndrome.The mutational landscape of recurrent versus nonrecurrent human papillomavirus-related oropharyngeal cancerThe Many Faces of Rap1 GTPase
P2860
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P2860
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@ast
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@en
type
label
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@ast
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@en
prefLabel
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@ast
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@en
P2093
P2860
P50
P356
P1476
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.
@en
P2093
A Francis Stewart
Andrea Kranz
Angela Matchan
Bernd Wollnik
Dagmar Wieczorek
Dian Donnai
E Ferda Percin
Esther Milz
Esther Pohl
Filippo Beleggia
P2860
P304
P356
10.1172/JCI80102
P407
P577
2015-08-17T00:00:00Z