Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
about
ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling.A dominant STIM1 mutation causes Stormorken syndrome.Ribosomal protein SA haploinsufficiency in humans with isolated congenital aspleniaIn vivo genome-wide analysis of multiple tissues identifies gene regulatory networks, novel functions and downstream regulatory genes for Bapx1 and its co-regulation with Sox9 in the mammalian vertebral column.Pbx1-dependent control of VMC differentiation kinetics underlies gross renal vascular patterning.Pbx Regulates Patterning of the Cerebral Cortex in Progenitors and Postmitotic NeuronsPbx4 is Required for the Temporal Onset of Zebrafish Myocardial DifferentiationNkx2-5(+)islet1(+) mesenchymal precursors generate distinct spleen stromal cell subsets and participate in restoring stromal network integrity.Liver-spleen axis: intersection between immunity, infections and metabolismPbx1 is required for adult subventricular zone neurogenesis.Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficienciesStromal cells of the mouse spleen.Glimpse into Hox and tale regulation of cell differentiation and reprogramming.ICON: the early diagnosis of congenital immunodeficiencies.PBX1 as Pioneer Factor: A Case Still Open.Transcription factor TLX1 controls retinoic acid signaling to ensure spleen development.Parallel Pbx-Dependent Pathways Govern the Coalescence and Fate of Motor Columns.Spleen hypoplasia leads to abnormal stress hematopoiesis in mice with loss of Pbx homeoproteins in splenic mesenchyme.Morphogenesis of the spleen during the human embryonic period.De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects.Pbx1 activates Fgf10 in the mesenchyme of developing lungs.PBX transcription factors drive pulmonary vascular adaptation to birth.Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion.[Connecting isolated congenital asplenia to the ribosome].Generation of a Tlx1(CreER-Venus) knock-in mouse strain for the study of spleen development.Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface., a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation inAlternative splicing links histone modifications to stem cell fate decision
P2860
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P2860
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@ast
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en-gb
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@nl
type
label
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@ast
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en-gb
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@nl
prefLabel
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@ast
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en-gb
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@nl
P2093
P2860
P50
P921
P1433
P1476
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module
@en
P2093
Alexandre Bolze
Andrea Brendolan
Ching-Pin Chang
Chisa Hidaka
Ekaterina Bojilova
Elisa Lenti
Licia Selleri
Mark Solloway
Matilde Saggese
Matthew Koss
P2860
P304
P356
10.1016/J.DEVCEL.2012.02.009
P407
P577
2012-05-15T00:00:00Z