Detalhe da pesquisa
1.
KGANSynergy: knowledge graph attention network for drug synergy prediction.
Brief Bioinform
; 24(3)2023 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37130580
2.
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.
Brain
; 146(8): 3347-3363, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869767
3.
Single-cell analysis of white adipose tissue reveals the tumor-promoting adipocyte subtypes.
J Transl Med
; 21(1): 470, 2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37454080
4.
Phase retrieval via nonlocal complex-domain sparsity.
Opt Lett
; 48(7): 1854-1857, 2023 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37221783
5.
Erratum: Trehalose inhibits H2O2-induced autophagic death in dopaminergic SH-SY5Y cells via mitigation of ROS-dependent endoplasmic reticulum stress and AMPK activation: Erratum.
Int J Med Sci
; 20(11): 1425-1426, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37790844
6.
Efficient large-scale single-pixel imaging.
Opt Lett
; 47(21): 5461-5464, 2022 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37219244
7.
Ultrahigh-security single-pixel semantic encryption.
Opt Lett
; 47(23): 6169-6172, 2022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37219199
8.
CNV profiles of Chinese pediatric patients with developmental disorders.
Genet Med
; 23(4): 669-678, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33402738
9.
Short-term and long-term safety and efficacy of tenofovir alafenamide, tenofovir disoproxil fumarate and entecavir treatment of acute-on-chronic liver failure associated with hepatitis B.
BMC Infect Dis
; 21(1): 567, 2021 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34126939
10.
[Autism spectrum disorder/development delay in siblings with SCN2A mutations caused by germline mosaicism].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(11): 1097-1100, 2021 Nov 10.
Artigo
em Zh
| MEDLINE | ID: mdl-34729751
11.
[Clinical features and gene variant of a pedigree affected with X-linked recessive mental retardation Claes-Jensen type].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(12): 1352-1355, 2020 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-33306820
12.
Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants.
BMC Med Genet
; 19(1): 21, 2018 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29422019
13.
Trehalose inhibits H2O2-induced autophagic death in dopaminergic SH-SY5Y cells via mitigation of ROS-dependent endoplasmic reticulum stress and AMPK activation.
Int J Med Sci
; 15(10): 1014-1024, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30013443
14.
[Clinical and genetic analysis of a patient with cutis laxa].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 100-103, 2018 Feb 10.
Artigo
em Zh
| MEDLINE | ID: mdl-29419872
15.
[A clinical and genetic analysis of a child with supernumerary marker chromosome 15-caused mental retardation, intractable epilepsy, and central precocious puberty].
Zhongguo Dang Dai Er Ke Za Zhi
; 20(8): 652-657, 2018 Aug.
Artigo
em Zh
| MEDLINE | ID: mdl-30111475
16.
[Glucose transporter 1 deficiency syndrome: features of movement disorders, diagnosis and treatment].
Zhongguo Dang Dai Er Ke Za Zhi
; 20(3): 209-213, 2018 Mar.
Artigo
em Zh
| MEDLINE | ID: mdl-29530121
17.
[Clinical and molecular genetic study of nonketotic hyperglycinemia in a Chinese family].
Zhongguo Dang Dai Er Ke Za Zhi
; 19(3): 268-271, 2017 Mar.
Artigo
em Zh
| MEDLINE | ID: mdl-28302194
18.
Cancer-associated fibroblast-derived gene signature discriminates distinct prognoses by integrated single-cell and bulk RNA-seq analyses in breast cancer.
Aging (Albany NY)
; 16(9): 8279-8305, 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38728370
19.
Identification and immunological role of cuproptosis in osteoporosis.
Heliyon
; 10(5): e26759, 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38455534
20.
Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutations.
J Hum Genet
; 58(4): 183-8, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23364391