Results 91 to 100 of about 1,393 (149)

Data Mining Analysis of <i>ESCO2</i> Gene Single Nucleotide Polymorphisms Associated with Roberts’s Syndrome [PDF]

, 2020
Sahar Mohamed Ali Mohamed Babiker, Afra M. Al Bkrye, Hind Abdelaziz Elnasri, Mona Abdelrahman Mohamed Khaier   +3 more
openalex   +1 more source

A rare case of fronto-nasal dystosis with multiple dysmorphic features: comprehensive genetic analysis using whole genome sequencing

Journal of Rare Diseases
Frontonasal dysostosis (FND) is a rare congenital disorder characterized by craniofacial abnormalities with diverse clinical characteristics. We report a four-year-old male with clinical characteristics related to frontonasal dysostosis, including ...
Sanjukta Sahoo, Deepak Jena, Mamuni Swain, Bhawna Gupta, Ravi Kant Narayan, Prabhas Ranjan Tripathy, Arun Kumar S, Manisha Rajanand Gaikwad, Sunil Kumar Raghav   +8 more
doaj   +1 more source

Cul4-Ddb1 ubiquitin ligases facilitate DNA replication-coupled sister chromatid cohesion through regulation of cohesin acetyltransferase Esco2 [PDF]

, 2018
Haitao Sun, Jiaxin Zhang, Jingjing Zhang, Zhen Li, Qinhong Cao, Huiqiang Lou   +5 more
openalex   +1 more source

Differential anti-viral response to respiratory syncytial virus A in preterm and term infantsResearch in context

EBioMedicine
Summary: Background: Preterm infants are more likely to experience severe respiratory syncytial virus (RSV) disease compared to term infants. The reasons for this are multi-factorial, however their immature immune system is believed to be a major ...
Jeremy Anderson, Samira Imran, Yan Yung Ng, Tongtong Wang, Sarah Ashley, Cao Minh Thang, Le Quang Thanh, Vo Thi Trang Dai, Phan Van Thanh, Bui Thi Hong Nhu, Do Ngoc Xuan Trang, Phan Thi Phuong Trinh, Le Thanh Binh, Nguyen Thuong Vu, Nguyen Trong Toan, Boris Novakovic, Mimi L.K. Tang, Danielle Wurzel, Kim Mulholland, Daniel G. Pellicci, Lien Anh Ha Do, Paul V. Licciardi   +21 more
doaj   +1 more source

Síndrome de Roberts asociado con inmunodeficiencia Roberts syndrome associated with immunodeficiency

Revista Cubana de Hematología, Inmunología y Hemoterapia, 2012
El síndrome de Roberts es una enfermedad genética de transmisión autosómica recesiva extremadamente rara. Se caracteriza clínicamente por retardo pre y posnatal del crecimiento, acortamiento severo de los miembros con defectos radiales, oligodactilia y ...
Miriam Sánchez-Segura, Vianed Marsán-Suárez, Consuelo Macías-Abraham, Norma de León-Ojeda, Alina García-García, Isabel Toledo-Rodríguez, Lázaro del Valle-Pérez, Berta Beatriz Socarrás-Ferrer   +7 more
doaj  

Síndrome de Roberts: presentación de caso y revisión de la literatura

Iatreia, 2010
Se presenta el caso de un feto con sospecha clínica de Síndrome de Roberts, nacido en Bogotá, de padres no consanguíneos. Se realiza documentación del caso, diagnósticos diferenciales y revisión de la literatura. Feto producto de primera gestación, madre
Yeinny Guatibonza Moreno, J. C. Prieto
doaj  

Identification of candidate genes related to hybrid sterility by genomic structural variation and transcriptome analyses in cattle-yak

Journal of Dairy Science
: Hybrids between closely related but genetically incompatible species are often inviable or sterile. Cattle-yak, an interspecific hybrid of yak and cattle, exhibits male-specific sterility, which limits the fixation of its desired traits and prevents ...
Rui-Dong Wan, Xue Gao, Guo-Wen Wang, Shi-Xin Wu, Qi-Lin Yang, Yi-Wen Zhang, Qi-En Yang   +6 more
doaj   +1 more source

Additional file 4 of ESCO2 promotes lung adenocarcinoma progression by regulating hnRNPA1 acetylation

, 2021
Hui-Er Zhu, Tao Li, Shengnan Shi, De-Xiong Chen, Weiping Chen, Hui Chen   +5 more
openalex   +1 more source

Temporal Regulation of ESCO2 Degradation by the MCM Complex, the CUL4-DDB1-VPRBP Complex, and the Anaphase-Promoting Complex [PDF]

, 2018
Masashi Minamino, Shoin Tei, Lumi Negishi, Masato T. Kanemaki, Atsunori Yoshimura, Takashi Sutani, Masashige Bando, Katsuhiko Shirahige   +7 more
openalex   +1 more source

ESCO2 promotes the proliferation of hepatocellular carcinoma through PI3K/AKT/ mTOR signaling pathway

Abstract Background: Establishment of sister chromatid cohesion N-Acetyltransferase 2(ESCO2), a gene reported to involved in the establishment of sister chromatid cohesion (SCC) and cell proliferation. We aim to explore how ESCO2 affects the proliferation of hepatocellular carcinoma (HCC).
Dapeng Chen, Yue Huang, Youcheng Zhang, Zhihong Zhang, Yamin Zhang   +4 more
openaire   +1 more source