Detalhe da pesquisa
1.
Sensory nerve regulates progenitor cells via FGF-SHH axis in tooth root morphogenesis.
Development
; 151(2)2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38108472
2.
Canonical Wnt signaling regulates soft palate development by mediating ciliary homeostasis.
Development
; 150(5)2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36825984
3.
Lhx6 regulates canonical Wnt signaling to control the fate of mesenchymal progenitor cells during mouse molar root patterning.
PLoS Genet
; 17(2): e1009320, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33596195
4.
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Mol Psychiatry
; 26(8): 4496-4510, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32015465
5.
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Hum Mol Genet
; 27(7): 1150-1163, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361080
6.
Mechano-chemical coupling of irrigation enhances endodontic biofilm debridement.
Biofouling
; 36(7): 792-799, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32873073
7.
Reduced dosage of ß-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
PLoS Genet
; 13(3): e1006687, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28346476
8.
A novel small deletion of LMX1B in a large Chinese family with nail-patella syndrome.
BMC Med Genet
; 20(1): 71, 2019 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31053111
9.
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Am J Hum Genet
; 97(6): 869-77, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26608785
10.
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Am J Hum Genet
; 96(5): 753-64, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25892112
11.
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.
Am J Med Genet A
; 176(10): 2172-2181, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30289625
12.
Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication.
Hum Mol Genet
; 23(16): 4215-31, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24705356
13.
p6gag domain confers cis HIV-1 Gag-Pol assembly and release capability.
J Gen Virol
; 97(1): 209-219, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26489905
14.
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Hum Genet
; 135(3): 273-85, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26742502
15.
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Am J Hum Genet
; 92(3): 439-47, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23453669
16.
A robust method for genome-wide association meta-analysis with the application to circulating insulin-like growth factor I concentrations.
Genet Epidemiol
; 38(2): 162-71, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24446417
17.
Vascular architecture regulates mesenchymal stromal cell heterogeneity via P53-PDGF signaling in the mouse incisor.
Cell Stem Cell
; 31(6): 904-920.e6, 2024 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703771
18.
Dynamic three-dimensional liver volume assessment of liver regeneration in hilar cholangiocarcinoma patients undergoing hemi-hepatectomy.
Front Oncol
; 14: 1375648, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38706591
19.
ARID1B maintains mesenchymal stem cell quiescence via inhibition of BCL11B-mediated non-canonical Activin signaling.
Nat Commun
; 15(1): 4614, 2024 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38816354
20.
A Prevascularized Sinus Tract on the Liver Surface for Islet Transplantation.
Transplantation
; 107(1): 117-128, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35758527