Genome-wide profiling in colorectal cancer identifies PHF19 and TBC1D16 as oncogenic super enhancers
2021 · Nature Communications · 128 citations
https://doi.org/10.1038/s41467-021-26600-5
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Xiang Lin
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Xiang Lin is an academic researcher from Shandong Provincial Hospital. The author has contributed to research in topics: Neurogenetic and Muscular Disorders Research & Hereditary Neurological Disorders & Neurological diseases and metabolism. The author has an h-index of 13, co-authored 40 publications.
ORCID: 0000-0002-1449-0114Papers by this author
worksSPOP suppresses prostate cancer through regulation of CYCLIN E1 stability
2018 · Cell Death and Differentiation · 53 citations
https://doi.org/10.1038/s41418-018-0198-0
Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons
2017 · Oncotarget · 25 citations
https://doi.org/10.18632/oncotarget.14641
Novel <i>CAPN1</i> mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia
2020 · Annals of Clinical and Translational Neurology · 14 citations
https://doi.org/10.1002/acn3.51169
Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia
2019 · Parkinsonism & Related Disorders · 11 citations
https://doi.org/10.1016/j.parkreldis.2019.06.008
Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)
2018 · Stem Cell Research · 8 citations
https://doi.org/10.1016/j.scr.2018.11.015
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