Detalhe da pesquisa
1.
Grainyhead-like 2 interacts with noggin to regulate tissue fusion in mouse.
Development
; 151(5)2024 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38300806
2.
Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects.
Dev Dyn
; 252(5): 647-667, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36606449
3.
Inhibition of retinoic acid signaling impairs cranial and spinal neural tube closure in mice lacking the Grainyhead-like 3 transcription factor.
Biochem Biophys Res Commun
; 635: 244-251, 2022 12 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36283337
4.
Delineating the roles of Grhl2 in craniofacial development through tissue-specific conditional deletion and epistasis approaches in mouse.
Dev Dyn
; 250(8): 1191-1209, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33638290
5.
Grainyhead-like transcription factors: guardians of the skin barrier.
Vet Dermatol
; 32(6): 553-e152, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-33843098
6.
Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome.
Am J Pathol
; 185(7): 1867-76, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-26093983
7.
Regulation of hematopoietic stem cells by their mature progeny.
Proc Natl Acad Sci U S A
; 107(50): 21689-94, 2010 Dec 14.
Artigo
Inglês
| MEDLINE | ID: mdl-21115812
8.
Critical roles for c-Myb in lymphoid priming and early B-cell development.
Blood
; 115(14): 2796-805, 2010 Apr 08.
Artigo
Inglês
| MEDLINE | ID: mdl-20130238
9.
Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure.
Dis Model Mech
; 13(3)2020 03 25.
Artigo
Inglês
| MEDLINE | ID: mdl-32005677
10.
An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome.
Sci Rep
; 8(1): 5482, 2018 04 03.
Artigo
Inglês
| MEDLINE | ID: mdl-29615807
11.
Stage-dependent therapeutic efficacy in PI3K/mTOR-driven squamous cell carcinoma of the skin.
Cell Death Differ
; 25(6): 1146-1159, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29238073
12.
A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination.
Dis Model Mech
; 7(6): 649-57, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24682784
13.
CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.
PLoS One
; 9(5): e97559, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-24840056
14.
Two ENU-induced alleles of Atp2b2 cause deafness in mice.
PLoS One
; 8(6): e67479, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-23826306
15.
Genetic Modifier Screens in Mice.
Curr Protoc Mouse Biol
; 2(1): 75-87, 2012 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26069006
16.
Vitamin D-deficient diet rescues hearing loss in Klotho mice.
Hear Res
; 275(1-2): 105-9, 2011 May.
Artigo
Inglês
| MEDLINE | ID: mdl-21167925
17.
Programmed anuclear cell death delimits platelet life span.
Cell
; 128(6): 1173-86, 2007 Mar 23.
Artigo
Inglês
| MEDLINE | ID: mdl-17382885
18.
A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopenia.
Proc Natl Acad Sci U S A
; 103(38): 14146-51, 2006 Sep 19.
Artigo
Inglês
| MEDLINE | ID: mdl-16966598
19.
Thrombocytopenia and kidney disease in mice with a mutation in the C1galt1 gene.
Proc Natl Acad Sci U S A
; 103(44): 16442-7, 2006 Oct 31.
Artigo
Inglês
| MEDLINE | ID: mdl-17062753
20.
Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene.
Blood
; 105(9): 3480-7, 2005 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-15665109