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1.
Small-molecule-induced epigenetic rejuvenation promotes SREBP condensation and overcomes barriers to CNS myelin regeneration.
Cell
; 187(10): 2465-2484.e22, 2024 May 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-38701782
2.
Olig2 targets chromatin remodelers to enhancers to initiate oligodendrocyte differentiation.
Cell
; 152(1-2): 248-61, 2013 Jan 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-23332759
3.
Microglia-organized scar-free spinal cord repair in neonatal mice.
Nature
; 587(7835): 613-618, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-33029008
4.
Effects of nitrate- and ammonium- nitrogen on anatomical and physiological responses of Catalpa bungei under full and partial root-zone drought.
BMC Plant Biol
; 24(1): 217, 2024 Mar 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-38532319
5.
Variants in BSN gene associated with epilepsy with favourable outcome.
J Med Genet
; 60(8): 776-783, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36600631
6.
Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients.
Neurogenetics
; 24(2): 129-136, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36802310
7.
Combined effects of high-fat diet and polystyrene microplastic exposure on microplastic bioaccumulation and lipid metabolism in zebrafish.
Fish Shellfish Immunol
; 137: 108803, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-37164123
8.
Unraveling the influential mechanism of short-chain branching on the crystallization of trimodal polyethylene by molecular dynamics simulation.
Phys Chem Chem Phys
; 25(27): 17912-17922, 2023 Jul 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37376922
9.
Ruthenium red attenuates acute pancreatitis by inhibiting MCU and improving mitochondrial function.
Biochem Biophys Res Commun
; 635: 236-243, 2022 12 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-36283336
10.
Genetic testing enables a precision medicine approach for nephrolithiasis and nephrocalcinosis in pediatrics: a single-center cohort.
Mol Genet Genomics
; 297(4): 1049-1061, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-35612621
11.
Molecular dynamics simulation of extension-induced crystallization of branched bimodal HDPE: Unraveling the effects of short-chain branches.
Phys Chem Chem Phys
; 23(35): 19862-19871, 2021 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-34525133
12.
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams.
Neurogenetics
; 21(2): 97-104, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31925597
13.
A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report.
BMC Med Genet
; 21(1): 166, 2020 08 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-32819290
14.
cDNA Library for Mining Functional Genes in Sedum alfredii Hance Related to Cadmium Tolerance and Characterization of the Roles of a Novel SaCTP2 Gene in Enhancing Cadmium Hyperaccumulation.
Environ Sci Technol
; 53(18): 10926-10940, 2019 Sep 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31449747
15.
Molecular dynamics simulation of shish-kebab crystallization of polyethylene: Unraveling the effects of molecular weight distribution.
J Chem Phys
; 150(18): 184114, 2019 May 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-31091915
16.
Identification and comprehensive analysis of the characteristics and roles of leucine-rich repeat receptor-like protein kinase (LRR-RLK) genes in Sedum alfredii Hance responding to cadmium stress.
Ecotoxicol Environ Saf
; 167: 95-106, 2019 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30312890
17.
[Phenotypic and genotypic analysis of a girl carrying a 2q22.3 microduplication encompassing the MBD5 gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(6): 624-627, 2019 Jun 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31055822
18.
[Genome-wide copy number microarray analysis for a boy with autism].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(2): 157-160, 2019 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-30703237
19.
[Clinical features and genetic analysis of a case with Coffin-Siris syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(5): 707-710, 2018 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-30298501
20.
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review.
BMC Med Genet
; 18(1): 141, 2017 12 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29191162