Results 181 to 190 of about 6,305,601 (337)

The Gut Resistome Atlas in Preterm Infants Enables Prediction of Necrotizing Enterocolitis Onset

Advanced Science, EarlyView.
The gut resistome of preterm infants and its clinical relevance remain poorly understood. This study performs in‐depth integrative analyses of 5,684 gut metagenomes from preterm infants, uncovering distinct features that diverge from term infants. Notably, the gut resistome of preterm infants converges 9 days before necrotizing enterocolitis onset ...
Shuqin Zeng, Hua Wang, Li Zhang, Shiping Li, Yuan Yuan, Mengting Tian, Yi Qu, Junjie Ying, Meicen Zhou, Yong Hu, Jinglan Huang, Rong Zou, Fengyan Zhao, Xiaojuan Su, Qian Liu, Yan He, Jinxing Feng, Weimin Huang, Ying Luo, Zhemin Zhou, Wei Shen, Dezhi Mu, Shaopu Wang   +22 more
wiley   +1 more source

X chromosome inactivation in mammals: general principles and species-specific considerations. [PDF]

EMBO Rep
Alfeghaly C, Rougeulle C.
europepmc   +1 more source

Physiological Aspects of Modification and Restoration of Chromosomal Synthesis in Bacteria After X Irradiation [PDF]

, 1965
Daniel Billen, Roger R. Hewitt
openalex   +1 more source

Xist recruits the X chromosome to the nuclear lamina to enable chromosome-wide silencing

Science, 2016
Chun-Kan Chen, M. Blanco, Constanza Jackson, E. Aznauryan, Noah Ollikainen, Christine Surka, A. Chow, A. Cerase, P. McDonel, M. Guttman   +9 more
semanticscholar   +1 more source

Tead1a Initiates Transcriptional Priming Through the TEAD1a/YAP‐Notch1‐Spi1/Cebpα Axis to Promote Neutrophil Fate

Advanced Science, EarlyView.
This study discovered that the protein TEAD1a is crucial for neutrophil development. In zebrafish models, disrupting TEAD1a or its interaction with partner protein YAP1 caused severe neutrophil deficiency. TEAD1a functions during the early HSC stage, activates Notch1 signaling in the GMP stage, and triggers Spi1 and Cebpα to drive neutrophil terminal ...
Wang Yiqin, Yang Ruimeng, Wang Peihong, Liu Xiaohui, Yuan Hao, Huang Hongli, Zhou Yongjian, Xie Baoshu   +7 more
wiley   +1 more source

Transcriptomic signatures of rare variant impacts across sex and the X chromosome. [PDF]

HGG Adv
Ungar RA, Li T, Vetr NG, Ersaro N, Battle A, Montgomery SB.   +5 more
europepmc   +1 more source

Preliminary Note on the Chromosome Alterations by X-rays in Loxoblemmus arictulus, a Species of Grylloid Family

, 1932
Kazuo Suzuki
openalex   +2 more sources

TRANSLOCATIONS BETWEEN THE X AND THE Y CHROMOSOMES OF DROSOPHILA MELANOGASTER [PDF]

, 1960
B. Nicoletti, Dan L. Lindsley
openalex   +1 more source

Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture

Proceedings of the National Academy of Sciences of the United States of America, 2016
E. Darrow, M. Huntley, O. Dudchenko, Elena K. Stamenova, Neva C. Durand, Zhuo Sun, Su-Chen Huang, Adrian L. Sanborn, Ido Machol, M. Shamim, Andrew P. Seberg, E. Lander, B. Chadwick, Erez Lieberman Aiden   +13 more
semanticscholar   +1 more source

Pathogenicity of Mediator Complex Subunit 27 (MED27) in a Neurodevelopmental Disorder with Cerebellar Atrophy

Advanced Science, EarlyView.
MED27 is one of the 26 subunits in the human Mediator complex (MED). Neurodevelopmental disorder‐causing MED27 genetic variants induce instability of MED, leading to disrupted DNA occupancy, altered chromatin interaction, and subsequent transcriptional dysregulation of critical downstream genes, including master regulatory transcription factors ...
Nuermila Yiliyaer, Xiaocheng Li, Tianyu Guo, Haiying Zhou, Lihai Gong, Luowei Yuan, Yang Fu, Yulong Qiao, Ying Lam Lui, Nuo Chen, Pengfei Lin, Hoi Hung Cheung, Ho Ko, Linyan Meng, Xiao Chen, Yong Lei, Kin Ming Kwan, Huating Wang, Shen Gu   +18 more
wiley   +1 more source