Detalhe da pesquisa
1.
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model.
Hum Mol Genet
; 2024 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38621658
2.
Endosome maturation links PI3Kα signaling to lysosome repopulation during basal autophagy.
EMBO J
; 41(19): e110398, 2022 10 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35968799
3.
AKT signaling promotes DNA damage accumulation and proliferation in polycystic kidney disease.
Hum Mol Genet
; 29(1): 31-48, 2020 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31625572
4.
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.
Hum Mol Genet
; 23(3): 618-36, 2014 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24087791
5.
FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation.
J Cell Sci
; 127(Pt 10): 2269-81, 2014 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24634512
6.
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Hum Mol Genet
; 21(14): 3237-54, 2012 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22523091
7.
A new role for phosphoinositides in regulating mitochondrial dynamics.
Adv Biol Regul
; 91: 101001, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38057188
8.
Sequential conversion of PtdIns3P to PtdIns(3,5)P2 via endosome maturation couples nutrient signaling to lysosome reformation and basal autophagy.
Autophagy
; 19(4): 1365-1367, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36103410
9.
Autophagic lysosome reformation in health and disease.
Autophagy
; 19(5): 1378-1395, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36409033
10.
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
J Clin Invest
; 118(3): 904-12, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18274675
11.
Bidirectional interconversion between PtdIns4P and PtdIns(4,5)P2 is required for autophagic lysosome reformation and protection from skeletal muscle disease.
Autophagy
; 17(5): 1287-1289, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33879025
12.
Defective lysosome reformation during autophagy causes skeletal muscle disease.
J Clin Invest
; 131(1)2021 01 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33119550
13.
Skeletal muscle NOX4 is required for adaptive responses that prevent insulin resistance.
Sci Adv
; 7(51): eabl4988, 2021 Dec 17.
Artigo
Inglês
| MEDLINE | ID: mdl-34910515
14.
SLIMMER (FHL1B/KyoT3) interacts with the proapoptotic protein Siva-1 (CD27BP) and delays skeletal myoblast apoptosis.
J Biol Chem
; 284(39): 26964-77, 2009 Sep 25.
Artigo
Inglês
| MEDLINE | ID: mdl-19643733
15.
Caveolae Control Contractile Tension for Epithelia to Eliminate Tumor Cells.
Dev Cell
; 54(1): 75-91.e7, 2020 07 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32485139
16.
Four and a half LIM protein 1: a partner for KCNA5 in human atrium.
Cardiovasc Res
; 78(3): 449-57, 2008 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-18281375
17.
FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).
PLoS One
; 10(2): e0117665, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25695429
18.
Regulation of the transcriptional coactivator FHL2 licenses activation of the androgen receptor in castrate-resistant prostate cancer.
Cancer Res
; 73(16): 5066-79, 2013 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23801747
19.
Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: a comprehensive review of the clinical, histological and pathological features.
Neuromuscul Disord
; 21(4): 237-51, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21310615
20.
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy.
J Cell Biol
; 183(6): 1033-48, 2008 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-19075112