Detalhe da pesquisa
1.
Correction: From Dynamic Expression Patterns to Boundary Formation in the Presomitic Mesoderm.
PLoS Comput Biol
; 15(7): e1007191, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31265460
2.
Modeling coexistence of oscillation and Delta/Notch-mediated lateral inhibition in pancreas development and neurogenesis.
J Theor Biol
; 430: 32-44, 2017 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28652000
3.
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
Mamm Genome
; 27(3-4): 111-21, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26803617
4.
Fast synchronization of ultradian oscillators controlled by delta-notch signaling with cis-inhibition.
PLoS Comput Biol
; 10(10): e1003843, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25275459
5.
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.
Hum Mol Genet
; 21(16): 3535-45, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22589248
6.
Domain-specific control of neurogenesis achieved through patterned regulation of Notch ligand expression.
Development
; 137(3): 437-45, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20081190
7.
From dynamic expression patterns to boundary formation in the presomitic mesoderm.
PLoS Comput Biol
; 8(6): e1002586, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22761566
8.
In vitro analysis of bone phenotypes in Col1a1 and Jagged1 mutant mice using a standardized osteoblast cell culture system.
J Bone Miner Metab
; 31(3): 293-303, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23371561
9.
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model.
Cell Death Discov
; 8(1): 387, 2022 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36115851
10.
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.
PLoS Genet
; 4(2): e7, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18248096
11.
A point mutation in the Pdia6 gene results in loss of pancreatic ß-cell identity causing overt diabetes.
Mol Metab
; 54: 101334, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34487921
12.
DLL1- and DLL4-Mediated Notch Signaling Is Essential for Adult Pancreatic Islet Homeostasis.
Diabetes
; 69(5): 915-926, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32029480
13.
PAX6 mutation alters circadian rhythm and ß cell function in mice without affecting glucose tolerance.
Commun Biol
; 3(1): 628, 2020 10 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33127955
14.
Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice.
Invest Ophthalmol Vis Sci
; 61(2): 44, 2020 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32106289
15.
A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.
Genetics
; 175(3): 1451-63, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17179084
16.
Cytoplasmic thioredoxin reductase is essential for embryogenesis but dispensable for cardiac development.
Mol Cell Biol
; 25(5): 1980-8, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15713651
17.
Point mutation of Ffar1 abrogates fatty acid-dependent insulin secretion, but protects against HFD-induced glucose intolerance.
Mol Metab
; 6(10): 1304-1312, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29031729
18.
Number of active transcription factor binding sites is essential for the Hes7 oscillator.
Theor Biol Med Model
; 3: 11, 2006 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-16504083
19.
Bezafibrate Improves Insulin Sensitivity and Metabolic Flexibility in STZ-Induced Diabetic Mice.
Diabetes
; 65(9): 2540-52, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27284107
20.
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.
G3 (Bethesda)
; 6(12): 4035-4046, 2016 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27815347