Ohcanbohtosat - Miriam Gordillo
- Čájehuvvo 1 - 8 / 8
-
1
Orchestrating liver development Dahkki Miriam Gordillo, Todd Evans, Valerie Gouon–Evans
Almmustuhtton 2015Revisão -
2
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion Dahkki Hugo Vega, Quinten Waisfisz, Miriam Gordillo, Norio Sakai, Itaru Yanagihara, Minoru Yamada, Djoke van Gosliga, Hülya Kayserili, Chengzhe Xu, Keiichi Ozono, Ethylin Wang Jabs, Koji Inui, Hans Joenje
Almmustuhtton 2005Artigo -
3
GATA6 regulates WNT and BMP programs to pattern precardiac mesoderm during the earliest stages of human cardiogenesis Dahkki J Bisson, Miriam Gordillo, Ritu Kumar, Neranjan de Silva, Ellen Yang, Kelly M. Banks, Zhong‐Dong Shi, Kihyun Lee, Dapeng Yang, Wendy K. Chung, Danwei Huangfu, Todd Evans
Almmustuhtton 2025Artigo -
4
A multi-organoid platform identifies CIART as a key factor for SARS-CoV-2 infection Dahkki Xuming Tang, Dongxiang Xue, Tuo Zhang, Benjamin E. Nilsson-Payant, Lucía Carrau, Xiaohua Duan, Miriam Gordillo, Adrian Y. Tan, Yunping Qiu, Jenny Xiang, Robert E. Schwartz, Benjamin R. tenOever, Todd Evans, Shuibing Chen
Almmustuhtton 2023Artigo -
5
Colonic organoids derived from human induced pluripotent stem cells for modeling colorectal cancer and drug testing Dahkki Miguel Crespo, Eduardo Vilar, Su‐Yi Tsai, Kyle Chang, Sadaf Amin, Tara Srinivasan, Tuo Zhang, Nina H. Pipalia, Huanhuan Joyce Chen, Mavee Witherspoon, Miriam Gordillo, Jenny Xiang, Frederick R. Maxfield, Steven M. Lipkin, Todd Evans, Shuibing Chen
Almmustuhtton 2017Artigo -
6
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes... Dahkki Horacio Astudillo‐de la Vega, Alison H. Trainer, Miriam Gordillo, Moira Crosier, Hülya Kayserili, Flemming Skovby, Maria Luisa Giovannucci Uzielli, Rhonda E. Schnur, Sylvie Manouvrier, E Blair, Jane A. Hurst, Francesca Forzano, Moritz Meins, K. O. J. Simola, Annick Raas‐Rothschild, Raoul C. M. Hennekam, Ethylin Wang Jabs
Almmustuhtton 2009Artigo -
7
Genome-scale screens identify JNK–JUN signaling as a barrier for pluripotency exit and endoderm differentiation Dahkki Qing V. Li, Gary Dixon, Nipun Verma, Bess P. Rosen, Miriam Gordillo, Renhe Luo, Chunlong Xu, Qiong Wang, Chew-Li Soh, Dapeng Yang, Miguel Crespo, Abhijit Shukla, Qing Xiang, Friederike Dündar, Paul Zumbo, Matthew D. Witkin, Richard P. Koche, Doron Betel, Shuibing Chen, Joan Massagué, Ralph Garippa, Todd Evans, M Beer, Danwei Huangfu
Almmustuhtton 2019Artigo -
8
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity Dahkki Miriam Gordillo, Hugo Vega, Alison H. Trainer, Fajian Hou, Norio Sakai, Ricardo Luque, Hülya Kayserili, Seher Başaran, Flemming Skovby, Raoul C. M. Hennekam, Maria Luisa Giovannucci Uzielli, Rhonda E. Schnur, Sylvie Manouvrier, Susan Chang, Edward Blair, Jane A. Hurst, Francesca Forzano, Moritz Meins, K. O. J. Simola, Annick Raas‐Rothschild, Roger A. Schultz, Lisa D. McDaniel, Keiichi Ozono, Koji Inui, Hui Zou, Ethylin Wang Jabs
Almmustuhtton 2008Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Gene
Genetics
Cell biology
Embryonic stem cell
Induced pluripotent stem cell
Phenotype
Stem cell
Transcription factor
Endoderm
Missense mutation
Molecular biology
Organoid
Signal transduction
Wnt signaling pathway
Adenomatous polyposis coli
Anatomy
Bioinformatics
Bone morphogenetic protein
Cancer
Cancer research
Cancer stem cell
Cell
Cellular differentiation
Centromere
Chromosome
Colorectal cancer
Computational biology
Developmental biology
Enhancer