about
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral refluxGenes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouseRai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and menCOP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblastInhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeInactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndromeMutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathyIdentification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.Therapeutic relevance of the protein phosphatase 2A in cancer.Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.Schimke immuno-osseous dysplasia: SMARCAL1 loss-of-function and phenotypic correlation.De novo acute myeloid leukemia with 20-29% blasts is less aggressive than acute myeloid leukemia with ≥30% blasts in older adults: a Bone Marrow Pathology Group study.
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-0536-8130
@en
name
Jiong Yan
@ast
Jiong Yan
@en
Jiong Yan
@es
Jiong Yan
@nl
type
label
Jiong Yan
@ast
Jiong Yan
@en
Jiong Yan
@es
Jiong Yan
@nl
prefLabel
Jiong Yan
@ast
Jiong Yan
@en
Jiong Yan
@es
Jiong Yan
@nl
P106
P1153
7403729299
P31
P496
0000-0003-0536-8130