Works matching IS 09646906 AND DT 2023 AND VI 32 AND IP 16

Results: 12

The PERK pathway: beneficial or detrimental for neurodegenerative diseases and tumor growth and cancer.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2545, doi. 10.1093/hmg/ddad103

By:

Talukdar, Gourango;
Orr, Harry T;
Lei, Zhixin

Publication type:

Article

Comprehensive analysis of autophagic functions of WIPI family proteins and their implications for the pathogenesis of β-propeller associated neurodegeneration.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2623, doi. 10.1093/hmg/ddad096

By:

Shimizu, Takahiro;
Tamura, Norito;
Nishimura, Taki;
Saito, Chieko;
Yamamoto, Hayashi;
Mizushima, Noboru

Publication type:

Article

Juvenile and adult expression of polyglutamine expanded huntingtin produce distinct aggregate distributions in Drosophila muscle.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2656, doi. 10.1093/hmg/ddad098

By:

Barwell, Taylor;
Raina, Sehaj;
Page, Austin;
MacCharles, Hayley;
Seroude, Laurent

Publication type:

Article

Correction to: Messenger RNA rescues medium-chain acyl-CoA dehydrogenase deficiency in fibroblasts from patients and a murine model.

Published in:: Human Molecular Genetics, 2023, v. 32, n. 16, p. 2679, doi. 10.1093/hmg/ddad116
Publication type:: Article

Metabolic liver cancer: associations of rare and common germline variants in one-carbon metabolism and DNA methylation genes.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2646, doi. 10.1093/hmg/ddad099

By:

Antwi, Samuel O;
Heckman, Michael;
White, Launia;
Yan, Irene;
Sarangi, Vivekananda;
Lauer, Kimberly P;
Reddy, Joseph;
Ahmed, Fowsiyo;
Veliginti, Swathi;
Febres, Ellis D Mejías;
Hatia, Rikita I;
Chang, Ping;
Izquierdo-Sanchez, Laura;
Boix, Loreto;
Rojas, Angela;
Banales, Jesus M;
Reig, Maria;
Stål, Per;
Gómez, Manuel Romero;
Singal, Amit G

Publication type:

Article

Stratified genome-wide association analysis of type 2 diabetes reveals subgroups with genetic and environmental heterogeneity.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2638, doi. 10.1093/hmg/ddad093

By:

Christiansen, Colette E;
Arathimos, Ryan;
Pain, Oliver;
Molokhia, Mariam;
Bell, Jordana T;
Lewis, Cathryn M

Publication type:

Article

5-Aminolevulinic acid bypasses mitochondrial complex I deficiency and corrects physiological dysfunctions in Drosophila.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2611, doi. 10.1093/hmg/ddad092

By:

Nozawa, Naoko;
Noguchi, Marie;
Shinno, Kanako;
Saito, Taro;
Asada, Akiko;
Ishii, Takuya;
Takahashi, Kiwamu;
Ishizuka, Masahiro;
Ando, Kanae

Publication type:

Article

Continuous, but not intermittent, regimens of hypoxia prevent and reverse ataxia in a murine model of Friedreich's ataxia.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2600, doi. 10.1093/hmg/ddad091

By:

Ast, Tslil;
Wang, Hong;
Marutani, Eizo;
Nagashima, Fumiaki;
Malhotra, Rajeev;
Ichinose, Fumito;
Mootha, Vamsi K

Publication type:

Article

Reticulons 1 and 3 are essential for axonal growth and synaptic maintenance associated with intellectual development.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2587, doi. 10.1093/hmg/ddad085

By:

Zhou, John;
Shi, Qi;
Ge, Ying Y;
He, Wanxia;
Hu, Xiangyou;
Xia, Weiming;
Yan, Riqiang

Publication type:

Article

Epigenome-wide methylation study identified two novel CpGs associated with T2DM risk and a network of co-methylated CpGs capable of patient's classifications.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2576, doi. 10.1093/hmg/ddad084

By:

Giri, Anil K;
Prasad, Gauri;
Parekatt, Vaisak;
Rajashekar, Donaka;
Tandon, Nikhil;
Bharadwaj, Dwaipayan

Publication type:

Article

Genome-wide association study identifies multiple HLA loci for sarcoidosis susceptibility.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2669, doi. 10.1093/hmg/ddad067

By:

Liao, Shu-Yi;
Jacobson, Sean;
Hamzeh, Nabeel Y;
Culver, Daniel A;
Barkes, Briana Q;
Mroz, Margarita;
Macphail, Kristyn;
Pacheco, Karin;
Patel, Divya C;
Wasfi, Yasmine S;
Koth, Laura L;
Langefeld, Carl D;
Leach, Sonia M;
White, Elizabeth;
Montgomery, Courtney;
Maier, Lisa A;
Fingerlin, Tasha E;
Investigators, GRADs

Publication type:

Article

NRSF regulates age-dependently cognitive ability and its conditional knockout in APP/PS1 mice moderately alters AD-like pathology.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 16, p. 2558, doi. 10.1093/hmg/ddac253

By:

Yang, Yufang;
Zhang, Xiaoshuang;
Li, Dongxue;
Fang, Rong;
Wang, Zishan;
Yun, Di;
Wang, Mo;
Wang, Jinghui;
Dong, Hongtian;
Fei, Zhaoliang;
Li, Qing;
Liu, Zhaolin;
Shen, Chenye;
Fei, Jian;
Yu, Mei;
Behnisch, Thomas;
Huang, Fang

Publication type:

Article