Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 22

Results: 12

Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2161, doi. 10.1093/hmg/ddab182

By:

Vashi, Neeti;
Ackerley, Cameron;
Post, Martin;
Justice, Monica J

Publication type:

Article

Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral density.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2177, doi. 10.1093/hmg/ddab181

By:

Bai, Wei-Yang;
Xia, Jiang-Wei;
Rong, Xiao-Li;
Cong, Pei-Kuan;
Khederzadeh, Saber;
Zheng, Hou-Feng

Publication type:

Article

Stress modulates Ahi1-dependent nuclear localization of ten-eleven translocation protein 2.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2149, doi. 10.1093/hmg/ddab179

By:

Zhang, Qian;
Hu, Qicheng;
Wang, Junjie;
Miao, Zhigang;
Li, Ziyi;
Zhao, Yuwen;
Wan, Bo;
Allen, Emily G;
Sun, Miao;
Jin, Peng;
Xu, Xingshun

Publication type:

Article

UHRF1 regulates alternative splicing by interacting with splicing factors and U snRNAs in a H3R2me involved manner.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2110, doi. 10.1093/hmg/ddab178

By:

Xu, Peng;
Zhang, Lan;
Xiao, Yao;
Li, Wei;
Hu, Zhiqiang;
Zhang, Rukui;
Li, Jin;
Wu, Feizhen;
Xi, Yanping;
Zou, Qingping;
Wang, Zhentian;
Guo, Rui;
Ma, Honghui;
Dong, Shihua;
Xiao, Min;
Yang, Zhicong;
Ren, Xiaoguang;
Wei, Chaochun;
Yu, Wenqiang

Publication type:

Article

Expression of Ripk1 and DAM genes correlates with severity and progression of Krabbe disease.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2082, doi. 10.1093/hmg/ddab159

By:

Cachón-González, María B;
Wang, Susan;
Cox, Timothy M

Publication type:

Article

ZNF224 is a mediator of TGF-β pro-oncogenic function in melanoma.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2100, doi. 10.1093/hmg/ddab173

By:

Cesaro, Elena;
Pastore, Arianna;
Polverino, Alessia;
Manna, Lorenzo;
Divisato, Giuseppina;
Quintavalle, Cristina;
Sanzo, Maddalena Di;
Faniello, Maria Concetta;
Grosso, Michela;
Costanzo, Paola

Publication type:

Article

Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2123, doi. 10.1093/hmg/ddab177

By:

Ongaro, Linda;
Mondal, Mayukh;
Flores, Rodrigo;
Marnetto, Davide;
Molinaro, Ludovica;
Alarcón-Riquelme, Marta E;
Moreno-Estrada, Andrés;
Mabunda, Nedio;
Ventura, Mario;
Tambets, Kristiina;
Hellenthal, Garrett;
Capelli, Cristian;
Kivisild, Toomas;
Metspalu, Mait;
Pagani, Luca;
Montinaro, Francesco

Publication type:

Article

Redefining the PTEN promoter: identification of novel upstream transcription start regions.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2135, doi. 10.1093/hmg/ddab175

By:

Grencewicz, Dennis J;
Romigh, Todd;
Thacker, Stetson;
Abbas, Ata;
Jaini, Ritika;
Luse, Donal;
Eng, Charis

Publication type:

Article

GWAS in Africans identifies novel lipids loci and demonstrates heterogenous association within Africa.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2205, doi. 10.1093/hmg/ddab174

By:

Bentley, Amy R;
Chen, Guanjie;
Doumatey, Ayo P;
Shriner, Daniel;
Meeks, Karlijn A C;
Gouveia, Mateus H;
Ekoru, Kenneth;
Zhou, Jie;
Adeyemo, Adebowale;
Rotimi, Charles N

Publication type:

Article

Prenatal inflammation as a link between placental expression signature of tryptophan metabolism and preterm birth.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2053, doi. 10.1093/hmg/ddab169

By:

Karahoda, Rona;
Robles, Morgane;
Marushka, Julia;
Stranik, Jaroslav;
Abad, Cilia;
Horackova, Hana;
Tebbens, Jurjen Duintjer;
Vaillancourt, Cathy;
Kacerovsky, Marian;
Staud, Frantisek

Publication type:

Article

Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2068, doi. 10.1093/hmg/ddab160

By:

Ravindran, Ethiraj;
Jühlen, Ramona;
Vieira-Vieira, Carlos H;
Ha, Thuong;
Salzberg, Yuval;
Fichtman, Boris;
Luise-Becker, Lena;
Martins, Nuno;
Picker-Minh, Sylvie;
Bessa, Paraskevi;
Arts, Peer;
Jackson, Matilda R;
Taranath, Ajay;
Kamien, Benjamin;
Barnett, Christopher;
Li, Na;
Tarabykin, Victor;
Stoltenburg-Didinger, Gisela;
Harel, Amnon;
Selbach, Matthias

Publication type:

Article

Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 22, p. 2190, doi. 10.1093/hmg/ddab166

By:

Justice, Anne E;
Young, Kristin;
Gogarten, Stephanie M;
Sofer, Tamar;
Graff, Misa;
Love, Shelly Ann M;
Wang, Yujie;
Klimentidis, Yann C;
Cruz, Miguel;
Guo, Xiuqing;
Hartwig, Fernando;
Petty, Lauren;
Yao, Jie;
Allison, Matthew A;
Below, Jennifer E;
Buchanan, Thomas A;
Chen, Yii-Der Ida;
Goodarzi, Mark O;
Hanis, Craig;
Highland, Heather M

Publication type:

Article