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A role of the frontotemporal lobar degeneration risk factor TMEM106B in myelination.
Published in:
2020
By:
- Feng, Tuancheng;
- Sheng, Rory R;
- Solé-Domènech, Santiago;
- Ullah, Mohammed;
- Zhou, Xiaolai;
- Mendoza, Christina S;
- Enriquez, Laura Camila Martinez;
- Katz, Isabel Iscol;
- Paushter, Daniel H;
- Sullivan, Peter M;
- Wu, Xiaochun;
- Maxfield, Frederick R;
- Hu, Fenghua
Publication type:
journal article
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function.
Published in:
Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43841-8
By:
- Okhovat, Mariam;
- VanCampen, Jake;
- Nevonen, Kimberly A.;
- Harshman, Lana;
- Li, Weiyu;
- Layman, Cora E.;
- Ward, Samantha;
- Herrera, Jarod;
- Wells, Jackson;
- Sheng, Rory R.;
- Mao, Yafei;
- Ndjamen, Blaise;
- Lima, Ana C.;
- Vigh-Conrad, Katinka A.;
- Stendahl, Alexandra M.;
- Yang, Ran;
- Fedorov, Lev;
- Matthews, Ian R.;
- Easow, Sarah A.;
- Chan, Dylan K.
Publication type:
Article
Loss of TMEM106B and PGRN leads to severe lysosomal abnormalities and neurodegeneration in mice.
Published in:
EMBO Reports, 2020, v. 21, n. 10, p. 1, doi. 10.15252/embr.202050219
By:
- Feng, Tuancheng;
- Mai, Shuyi;
- Roscoe, Jenn Marie;
- Sheng, Rory R;
- Ullah, Mohammed;
- Zhang, Junke;
- Katz, Isabel Iscol;
- Yu, Haiyuan;
- Xiong, Wenjun;
- Hu, Fenghua
Publication type:
Article
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Published in:
eLife, 2024, p. 1, doi. 10.7554/eLife.89762
By:
- Hao Yu;
- Khanshour, Anas M.;
- Ushiki, Aki;
- Nao Otomo;
- Yoshinao Koike;
- Einarsdottir, Elisabet;
- Yanhui Fan;
- Antunes, Lilian;
- Kidane, Yared H.;
- Cornelia, Reuel;
- Sheng, Rory R.;
- Yichi Zhang;
- Pei, Jimin;
- Grishin, Nick V.;
- Evers, Bret M.;
- Cheung, Jason Pui Yin;
- Herring, John A.;
- Chikashi Terao;
- You-qiang Song;
- Gurnett, Christina A.
Publication type:
Article

Found: 4

A role of the frontotemporal lobar degeneration risk factor TMEM106B in myelination.

TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function.

Loss of TMEM106B and PGRN leads to severe lysosomal abnormalities and neurodegeneration in mice.

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.