Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Yandi Gao"'
Autor:
Haiwen Li, Li Xu, Yandi Gao, Yuanbojiao Zuo, Zuocheng Yang, Lingling Zhao, Zhiheng Chen, Shuliang Guo, Renzhi Han
Publikováno v:
Cell & Bioscience, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Background Anoctamin 5 (ANO5) is a membrane protein belonging to the TMEM16/Anoctamin family and its deficiency leads to the development of limb girdle muscular dystrophy R12 (LGMDR12). However, little has been known about the interactome of
Externí odkaz:
https://doaj.org/article/99cd3c1a60db422eb807ecc673406573
Autor:
Li Xu, Chen Zhang, Haiwen Li, Peipei Wang, Yandi Gao, Nahush A. Mokadam, Jianjie Ma, W. David Arnold, Renzhi Han
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Base editing is one approach used to correct mutations causing cause Duchenne muscular dystrophy (DMD), but limitations are in the requirement for a specific PAM motif and the large size beyond the packaging capacity of adeno-associated virus (AAV).
Externí odkaz:
https://doaj.org/article/e267fd77833f4da08de183661fa8161a
Autor:
Katiri J. Snyder, Hannah K. Choe, Yandi Gao, Natalie E. Sell, Kara M. Braunreiter, Nina C. Zitzer, Lotus Neidemire-Colley, Sonu Kalyan, Adrienne M. Dorrance, Andrea Keller, Maria M. Mihaylova, Satishkumar Singh, Lalit Sehgal, Gideon Bollag, Yan Ma, Ben Powell, Steven M. Devine, Parvathi Ranganathan
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Acute graft-versus-host disease (GVHD) is the leading cause of non-relapse mortality following allogeneic hematopoietic cell transplantation. The majority of patients non-responsive to front line treatment with steroids have an estimated overall 2-ye
Externí odkaz:
https://doaj.org/article/56efe39a20fb494faaa4960077ed69ab
Publikováno v:
Skeletal Muscle, Vol 8, Iss 1, Pp 1-9 (2018)
Abstract Background Histological assessment of skeletal muscle sections is important for the research of muscle physiology and diseases. Quantifiable measures of skeletal muscle often include mean fiber diameter, fiber size distribution, and centrall
Externí odkaz:
https://doaj.org/article/83361752021a4688977570876dcbbdc0
Autor:
Tingting Sui, Li Xu, Yeh Siang Lau, Di Liu, Tingjun Liu, Yandi Gao, Liangxue Lai, Renzhi Han, Zhanjun Li
Publikováno v:
Cell Death and Disease, Vol 11, Iss 6, Pp 1-2 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/fa485c5ac2574fa295a1fa81de308963
Autor:
Tingting Sui, Yeh Siang Lau, Di Liu, Tingjun Liu, Li Xu, Yandi Gao, Liangxue Lai, Zhanjun Li, Renzhi Han
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 6 (2018)
Duchenne muscular dystrophy (DMD) is an X-linked muscle-wasting disorder caused by mutations in the dystrophin gene, with an incidence of 1 in 3500 in new male births. Mdx mice are widely used as an animal model for DMD. However, these mice do not fa
Externí odkaz:
https://doaj.org/article/d5feaa7ac65c43d7adddc02623bb799f
Autor:
Kwok-Kin Wong, James E. Bradner, Andrew L. Kung, Alec C. Kimmelman, Esra Akbay, Jun Qi, Travis J. Cohoon, Katherine A. Cheng, Yandi Gao, Jeremy H. Tchaicha, Eiki Kikuchi, Julian Carretero, Margaret Soucheray, Zhao Chen, Takeshi Shimamura
Supplementary Methods - PDF file 201K, Supplementary Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72be80fab1281c24a4b711015d370301
https://doi.org/10.1158/1078-0432.22452194
https://doi.org/10.1158/1078-0432.22452194
Autor:
Takeshi Shimamura, Julian Carretero, Kwok-Kin Wong, Pasi A. Jänne, Oscar Juan, Amelia Insa, Agustín Lahoz, Jeffrey A. Borgia, Fatima Al-Shahrour, Michael P. Kahle, Hajime Asahina, Ashley Hess, Patricia Simms, Camilla L. Christensen, Javier Alcácer, José M. Galbis-Caravajal, Antonio Cremades, Paloma Martín-Martorell, Javier Alcácer Fernández-Coronado, Miguel Aupí, Aranzazu Lafuente-Sanchis, Rutu Gandhi, María L. Rodríguez, Eiki Kikuchi, Ines Pulido, Margaret Soucheray, Yandi Gao, Jeffrey H. Becker
Supplementary Figure Legends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86f54a9e01b8e39179663f1e9a598dbc
https://doi.org/10.1158/0008-5472.22421373.v1
https://doi.org/10.1158/0008-5472.22421373.v1
Autor:
Takeshi Shimamura, Julian Carretero, Kwok-Kin Wong, Pasi A. Jänne, Oscar Juan, Amelia Insa, Agustín Lahoz, Jeffrey A. Borgia, Fatima Al-Shahrour, Michael P. Kahle, Hajime Asahina, Ashley Hess, Patricia Simms, Camilla L. Christensen, Javier Alcácer, José M. Galbis-Caravajal, Antonio Cremades, Paloma Martín-Martorell, Javier Alcácer Fernández-Coronado, Miguel Aupí, Aranzazu Lafuente-Sanchis, Rutu Gandhi, María L. Rodríguez, Eiki Kikuchi, Ines Pulido, Margaret Soucheray, Yandi Gao, Jeffrey H. Becker
Supplementary Figures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b60c5db3d8550b9937a2d7c74f5be54
https://doi.org/10.1158/0008-5472.22421370
https://doi.org/10.1158/0008-5472.22421370
Autor:
Takeshi Shimamura, Julian Carretero, Kwok-Kin Wong, Pasi A. Jänne, Oscar Juan, Amelia Insa, Agustín Lahoz, Jeffrey A. Borgia, Fatima Al-Shahrour, Michael P. Kahle, Hajime Asahina, Ashley Hess, Patricia Simms, Camilla L. Christensen, Javier Alcácer, José M. Galbis-Caravajal, Antonio Cremades, Paloma Martín-Martorell, Javier Alcácer Fernández-Coronado, Miguel Aupí, Aranzazu Lafuente-Sanchis, Rutu Gandhi, María L. Rodríguez, Eiki Kikuchi, Ines Pulido, Margaret Soucheray, Yandi Gao, Jeffrey H. Becker
Although EGFR mutant–selective tyrosine kinase inhibitors (TKI) are clinically effective, acquired resistance can occur by reactivating ERK. We show using in vitro models of acquired EGFR TKI resistance with a mesenchymal phenotype that CXCR7, an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a163c2049abde7c57bdfad3ee9c80405
https://doi.org/10.1158/0008-5472.c.6510909.v1
https://doi.org/10.1158/0008-5472.c.6510909.v1