Detalhe da pesquisa
1.
Enhancer divergence and cis-regulatory evolution in the human and chimp neural crest.
Cell
; 163(1): 68-83, 2015 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26365491
2.
Shaping faces: genetic and epigenetic control of craniofacial morphogenesis.
Nat Rev Genet
; 24(9): 610-626, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37095271
3.
'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks.
Genes Dev
; 33(5-6): 258-275, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30824532
4.
ESCRT-dependent control of craniofacial morphogenesis with concomitant perturbation of NOTCH signaling.
Dev Biol
; 503: 25-42, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37573008
5.
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
Development
; 147(18)2020 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32958507
6.
Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease.
Hum Mol Genet
; 29(7): 1068-1082, 2020 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31625560
7.
Corrigendum: 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks.
Genes Dev
; 33(9-10): 590, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31043493
8.
Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion.
Development
; 145(5)2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29437830
9.
Ubiquitous overexpression of CXCL12 confers radiation protection and enhances mobilization of hematopoietic stem and progenitor cells.
Stem Cells
; 38(9): 1159-1174, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32442338
10.
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons.
Proc Natl Acad Sci U S A
; 115(34): E8007-E8016, 2018 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30072435
11.
The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo.
EMBO J
; 40(2): e107130, 2021 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33448440
12.
A PBX1 transcriptional network controls dopaminergic neuron development and is impaired in Parkinson's disease.
EMBO J
; 35(18): 1963-78, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27354364
13.
De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects.
Hum Mol Genet
; 26(24): 4849-4860, 2017 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29036646
14.
Pbx1 is required for adult subventricular zone neurogenesis.
Development
; 143(13): 2281-91, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27226325
15.
The FaceBase Consortium: a comprehensive resource for craniofacial researchers.
Development
; 143(14): 2677-88, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287806
16.
Pbx1-dependent control of VMC differentiation kinetics underlies gross renal vascular patterning.
Development
; 142(15): 2653-64, 2015 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26138478
17.
Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface.
J Anat
; 233(2): 222-242, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29797482
18.
The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo.
EMBO J
; 31(20): 4045-56, 2012 Oct 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22940690
19.
Spleen hypoplasia leads to abnormal stress hematopoiesis in mice with loss of Pbx homeoproteins in splenic mesenchyme.
J Anat
; 229(1): 153-69, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27075259
20.
Pbx1 activates Fgf10 in the mesenchyme of developing lungs.
Genesis
; 52(5): 399-407, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24591256