A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
about
Highly conserved non-coding sequences are associated with vertebrate developmentVACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arraysInvolvement of the HLXB9 homeobox gene in Currarino syndromeMutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis.VACTERL/VATER AssociationA genomewide association study of citalopram response in major depressive disorderHuman HOX gene mutationsEmbryonic gut anomalies in a mouse model of retinoic Acid-induced caudal regression syndrome: delayed gut looping, rudimentary cecum, and anorectal anomaliesAnorectal malformations caused by defects in sonic hedgehog signalingEctopic expression of Ptf1a induces spinal defects, urogenital defects, and anorectal malformations in Danforth's short tail mice.Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1.Update on the cytogenetics and molecular genetics of chordomaMany faces of monogenic diabetesMicrocephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q.Birth defects associated with perturbations in preimplantation, gastrulation, and axis extension: from conjoined twinning to caudal dysgenesis.Autosomal dominant sacral agenesis: Currarino syndrome.t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia.Mutation analysis of a large Chinese pedigree with congenital preaxial polydactyly.HLXB9 activates IL6 in Hodgkin lymphoma cell lines and is regulated by PI3K signalling involving E2F3.Currarino syndrome in an adult presenting with a presacral abscess: a case report.Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression.A retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse.Leiomyomatosis peritonealis disseminata in association with Currarino syndrome?Development and diseases of the pancreas.A clinical and experimental overview of sirenomelia: insight into the mechanisms of congenital limb malformations."This bicycle gives me a headache", a congenital anomaly.Telomeres: a diagnosis at the end of the chromosomesZebrafish mnx1 controls cell fate choice in the developing endocrine pancreas.Sacral agenesis: a pilot whole exome sequencing and copy number study.The Currarino triad: neurosurgical considerations.Currarino triad with Müllerian duct anomaly in mother and daughter without MNX1 gene mutation.Neurogenic bladder: etiology and assessment.Short-term surviving sirenomelia neonate followed by a complex mesodermal malformation in a sibling.A tail of sacral agenesis: delayed presentation of meningocele in sacral agenesis.Sacral agenesis and neurogenic bladder: Long-term outcomes of bladder and kidney function.Fatal Meningitis in a 14-Month-Old with Currarino Triad.New horizons at the caudal embryos: coordinated urogenital/reproductive organ formation by growth factor signaling.Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.
P2860
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P2860
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
description
1998 nî lūn-bûn
@nan
1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@ast
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en-gb
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@nl
type
label
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@ast
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en-gb
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@nl
prefLabel
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@ast
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en-gb
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis
@en
P2093
Monclair T
Orstavik KH
P2860
P2888
P304
P3181
P356
10.1038/3828
P407
P577
1998-12-01T00:00:00Z
P6179
1030872162