Detalhe da pesquisa
1.
MCC is a centrosomal protein that relocalizes to non-centrosomal apical sites during intestinal cell differentiation.
J Cell Sci
; 135(21)2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36217793
2.
No NFATC2 fusion in simple bone cyst of the jaw.
Histopathology
; 83(2): 326-329, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-36939112
3.
Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype.
Hum Mol Genet
; 27(16): 2775-2788, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29741626
4.
MINDY1 Is a Downstream Target of the Polyamines and Promotes Embryonic Stem Cell Self-Renewal.
Stem Cells
; 36(8): 1170-1178, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29644784
5.
The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish.
Development
; 141(18): 3505-16, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25183869
6.
The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the ß-Arrestin Pathway.
Cells
; 13(3)2024 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38334624
7.
Identification of stable housekeeping genes for induced pluripotent stem cells and -derived endothelial cells for drug testing.
Sci Rep
; 12(1): 16160, 2022 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36171445
8.
Gene fusions in vascular tumors and their underlying molecular mechanisms.
Expert Rev Mol Diagn
; 21(9): 897-909, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34225547
9.
Expanding the Spectrum of EWSR1-NFATC2-rearranged Benign Tumors: A Common Genomic Abnormality in Vascular Malformation/Hemangioma and Simple Bone Cyst.
Am J Surg Pathol
; 45(12): 1669-1681, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34081036
10.
Unintended consequences of infection prevention and control measures during COVID-19 pandemic.
Am J Infect Control
; 49(4): 469-477, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33157180
11.
Microfibril-associated glycoprotein 4 (Mfap4) regulates haematopoiesis in zebrafish.
Sci Rep
; 10(1): 11801, 2020 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32678226
12.
The novel zebrafish model pretzel demonstrates a central role for SH3PXD2B in defective collagen remodelling and fibrosis in Frank-Ter Haar syndrome.
Biol Open
; 9(12)2020 12 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33234702
13.
PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly.
Sci Adv
; 6(2): eaax9852, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31950080
14.
Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells.
Stem Cell Reports
; 8(6): 1675-1688, 2017 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28591650
15.
ELABELA deficiency promotes preeclampsia and cardiovascular malformations in mice.
Science
; 357(6352): 707-713, 2017 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28663440
16.
PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signaling.
Nat Genet
; 49(9): 1354-1363, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28740264