Detalhe da pesquisa
1.
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5.
EMBO J
; 41(17): e110784, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35859387
2.
Ablation of mitochondrial DNA results in widespread remodeling of the mitochondrial complexome.
EMBO J
; 40(21): e108648, 2021 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34542926
3.
Evolutionary pathways to lower biomass allocation to the seed coat in crops: insights from allometric scaling.
New Phytol
; 243(1): 466-476, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38757753
4.
The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria.
Mol Cell
; 64(1): 148-162, 2016 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27642048
5.
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences.
Brain
; 145(7): 2602-2616, 2022 07 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35104841
6.
Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.
Am J Hum Genet
; 102(4): 685-695, 2018 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29576219
7.
Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.
Genet Med
; 23(9): 1705-1714, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34140661
8.
Use of deuterium oxide (2H2O) to assess muscle protein synthesis in juvenile red drum (Sciaenops ocellatus) fed complete, and valine-deficient diets.
Amino Acids
; 53(9): 1431-1439, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34232398
9.
Infected hepatic echinococcosis. Clinical, therapeutic, and prognostic aspects. A systematic review.
Ann Hepatol
; 22: 100237, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32835861
10.
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.
Am J Hum Genet
; 100(2): 216-227, 2017 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28065471
11.
COmplexome Profiling ALignment (COPAL) reveals remodeling of mitochondrial protein complexes in Barth syndrome.
Bioinformatics
; 35(17): 3083-3091, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30649188
12.
Novel defect in phosphatidylinositol 4-kinase type 2-alpha (PI4K2A) at the membrane-enzyme interface is associated with metabolic cutis laxa.
J Inherit Metab Dis
; 43(6): 1382-1391, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32418222
13.
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome.
Hum Mol Genet
; 26(13): 2541-2550, 2017 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28449065
14.
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I Deficiency.
Am J Hum Genet
; 99(1): 208-16, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27374773
15.
Electroacupuncture and Curcumin Promote Oxidative Balance and Motor Function Recovery in Rats Following Traumatic Spinal Cord Injury.
Neurochem Res
; 44(2): 498-506, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30603981
16.
Modafinil for people with schizophrenia or related disorders.
Cochrane Database Syst Rev
; 12: CD008661, 2019 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31828767
17.
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.
Am J Hum Genet
; 107(2): 374, 2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32763190
18.
Accessory NUMM (NDUFS6) subunit harbors a Zn-binding site and is essential for biogenesis of mitochondrial complex I.
Proc Natl Acad Sci U S A
; 112(18): 5685-90, 2015 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25902503
19.
Synthesis and Characterization of Poly(Vinyl Alcohol)-Chitosan-Hydroxyapatite Scaffolds: A Promising Alternative for Bone Tissue Regeneration.
Molecules
; 23(10)2018 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30241366
20.
Identification and evolutionary analysis of tissue-specific isoforms of mitochondrial complex I subunit NDUFV3.
Biochim Biophys Acta Bioenerg
; 1858(3): 208-217, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27988283