Detalhe da pesquisa
1.
Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.
Nature
; 567(7747): E5-E9, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30814738
2.
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings.
PLoS Genet
; 17(7): e1009639, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34232960
3.
SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins.
Hum Mol Genet
; 29(24): 3882-3891, 2021 02 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33355670
4.
High-speed counter-current chromatography assisted preparative isolation of phenolic compounds from the flowers of Chrysanthemum morifolium cv. Fubaiju.
J Sep Sci
; 46(19): e2300172, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37528737
5.
Pathways to improve energy efficiency under carbon emission constraints in iron and steel industry: Using EBM, NCA and QCA approaches.
J Environ Manage
; 348: 119206, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37898049
6.
Metagenomics reveals taxon-specific responses of soil nitrogen cycling under different fertilization regimes in heavy metal contaminated soil.
J Environ Manage
; 345: 118766, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37579601
7.
Melatonin Attenuates Vascular Smooth Muscle Contraction Through the γ-Secretase/Notch Intracellular Domain/Myocardin Pathway.
J Cardiovasc Pharmacol
; 80(4): 574-582, 2022 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35881905
8.
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.
Nature
; 540(7632): 270-275, 2016 12 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27919073
9.
Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation.
Am J Pathol
; 190(12): 2453-2463, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32919980
10.
Biparental Inheritance of Mitochondrial DNA in Humans.
Proc Natl Acad Sci U S A
; 115(51): 13039-13044, 2018 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30478036
11.
Striated Preferentially Expressed Protein Kinase (SPEG) in Muscle Development, Function, and Disease.
Int J Mol Sci
; 22(11)2021 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34072258
12.
Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima.
Neurobiol Dis
; 143: 105013, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32653676
13.
Correction: Li, et al. LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer Cells. Int. J. Mol. Sci. 2019, 20, 3616.
Int J Mol Sci
; 21(15)2020 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32825207
14.
Effects of oral monosodium glutamate administration on serum metabolomics of suckling piglets.
J Anim Physiol Anim Nutr (Berl)
; 104(1): 269-279, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31553089
15.
LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer Cells.
Int J Mol Sci
; 20(15)2019 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31344855
16.
[Genetic testing and pregnancy outcome of 337 fetuses with urinary system anomalies].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(4): 306-309, 2019 Apr 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30950013
17.
Live birth derived from oocyte spindle transfer to prevent mitochondrial disease.
Reprod Biomed Online
; 34(4): 361-368, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385334
18.
Reply to Annis et al.: Is quasi-Mendelian mtDNA competition enough to drive transmission of paternal mtDNA?
Proc Natl Acad Sci U S A
; 116(30): 14799-14800, 2019 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31311873
19.
Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments.
Proc Natl Acad Sci U S A
; 116(6): 1823-1824, 2019 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30674682
20.
[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(3): 321-326, 2017 Jun 10.
Artigo
em Zh
| MEDLINE | ID: mdl-28604947