Detalhe da pesquisa
1.
ZAKß is activated by cellular compression and mediates contraction-induced MAP kinase signaling in skeletal muscle.
EMBO J;
41(17): e111650, 2022 09 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35899396
2.
Myofibrillar myopathy hallmarks associated with ZAK deficiency.
Hum Mol Genet;
32(17): 2751-2770, 2023 08 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37427997
3.
High-throughput RNA sequencing of the T cell receptor alpha and beta chains for simultaneous clonality and biological analyses in Sezary syndrome.
J Clin Lab Anal;
37(23-24): e24982, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38115685
4.
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
Int J Mol Sci;
24(9)2023 Apr 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37175717
5.
Proteomic resolution of IGFN1 complexes reveals a functional interaction with the actin nucleating protein COBL.
Exp Cell Res;
395(2): 112179, 2020 10 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32768501
6.
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
Hum Mol Genet;
27(10): 1723-1731, 2018 05 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29509900
7.
The CLE53-SUNN genetic pathway negatively regulates arbuscular mycorrhiza root colonization in Medicago truncatula.
J Exp Bot;
71(16): 4972-4984, 2020 08 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32309861
8.
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion.
Brain;
140(1): 37-48, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27816943
9.
Disrupted autophagy undermines skeletal muscle adaptation and integrity.
Mamm Genome;
27(11-12): 525-537, 2016 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27484057
10.
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.
Brain;
137(Pt 12): 3171-85, 2014 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25348630
11.
Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: different genetic mechanisms but equivalent poorer clinical outcome.
Genes Chromosomes Cancer;
53(9): 788-97, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24915757
12.
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.
Hum Mol Genet;
21(8): 1706-24, 2012 Apr 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22199023
13.
Proteomic analysis of laser capture microscopy purified myotendinous junction regions from muscle sections.
Proteome Sci;
12: 25, 2014.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25071420
14.
Expanding science skills: teaching tissue culture, data analysis, and reporting through imaging the actin cytoskeleton.
J Microbiol Biol Educ;
: e0019023, 2024 May 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38722163
15.
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
Nat Genet;
34(4): 421-8, 2003 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12833159
16.
Efficacy of modified active packaging with oxygen scavengers for the preservation of sliced Iberian dry-cured shoulder.
Food Sci Technol Int;
29(4): 318-330, 2023 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35225018
17.
Ex Vivo Maturation of 3D-Printed, Chondrocyte-Laden, Polycaprolactone-Based Scaffolds Prior to Transplantation Improves Engineered Cartilage Substitute Properties and Integration.
Cartilage;
13(4): 105-118, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36250422
18.
Sézary syndrome patient-derived models allow drug selection for personalized therapy.
Blood Adv;
6(11): 3410-3421, 2022 06 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35413113
19.
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse.
Hum Mol Genet;
18(19): 3553-66, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19578180
20.
Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1.
Exp Cell Res;
316(11): 1856-70, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20206623