Shifeng Xue

发表

RNA regulons in Hox 5′UTRs confer ribosome specificity to gene regulation

Rhiju Das, Shifeng Xue, Siqi Tian, 2014, Nature.

Specialized ribosomes: a new frontier in gene regulation and organismal biology

Shifeng Xue, M. Barna, 2012, Nature Reviews Molecular Cell Biology.

FSHD2- and BAMS-associated mutations confer opposing effects on SMCHD1 function

Shifeng Xue, Weiwen Dai, M. Blewitt, 2018, The Journal of Biological Chemistry.

HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring

Shifeng Xue, F. Magdinier, A. Mathuru, 2022, Nature Communications.

Direct identification of A-to-I editing sites with nanopore native RNA sequencing

Shifeng Xue, M. Šikić, Y. Wan, 2022, Nature Methods.

Cis-regulatory RNA elements that regulate specialized ribosome activity

Shifeng Xue, M. Barna, 2015, RNA biology.

Ribosome-Mediated Specificity in Hox mRNA Translation and Vertebrate Tissue Patterning

Shifeng Xue, M. Barna, A. Hsieh, 2011, Cell.

SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite

Shifeng Xue, F. Magdinier, B. Wollnik, 2019, Nucleic acids research.

Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndrome

Abdullah, Shifeng Xue, W. Ahmad, 2021, Journal of Human Genetics.

Gene- and Species-Specific Hox mRNA Translation by Ribosome Expansion Segments.

Shifeng Xue, K. Fujii, M. Barna, 2020, Molecular cell.

SMCHD1 variants may induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome

Shifeng Xue, F. Magdinier, J. Déjardin, 2021, bioRxiv.

SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease

Matthew E. Ritchie, A. Keniry, Shifeng Xue, 2021, bioRxiv.

SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite

Shifeng Xue, F. Magdinier, Christopher, 2019, Nucleic acids research.

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

Asif Javed, Shifeng Xue, H. Kayserili, 2017, Nature Genetics.

Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen storage-associated mitochondriopathy.

Fernanda L. Sirota, J. Lupski, J. Casanova, 2021, American journal of human genetics.

AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome

Shifeng Xue, F. Magdinier, E. Novoa-Del-Toro, 2021, Biomedicines.

A novel variant in AFF3 underlying isolated syndactyly

Shifeng Xue, W. Ahmad, Shabir Hussain, 2022, Clinical genetics.

In skeletal muscle and neural crest cells, SMCHD1 regulates biological pathways relevant for Bosma syndrome and facioscapulohumeral dystrophy phenotype

Shifeng Xue, F. Magdinier, J. Déjardin, 2023, Nucleic acids research.

Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita.

B. Venkatesh, M. Gut, I. Gut, 2017, American journal of human genetics.

Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish

Fernanda L. Sirota, J. Lupski, J. Casanova, 2021, medRxiv.