User profiles for "author:Mingchu Xu"
Mingchu XuAmazon Verified email at amazon.com Cited by 1498 |
Prognostic role of systemic inflammatory response in renal cell carcinoma: a systematic review and meta-analysis
Purpose To summarize the global predicting role of systemic inflammatory response for
survival in renal cell carcinoma. Methods Eligible studies were identified and assessed for …
survival in renal cell carcinoma. Methods Eligible studies were identified and assessed for …
[HTML][HTML] Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer
EH Lips, T Kumar, A Megalios, LL Visser… - Nature …, 2022 - nature.com
Ductal carcinoma in situ (DCIS) is the most common form of preinvasive breast cancer and,
despite treatment, a small fraction (5–10%) of DCIS patients develop subsequent invasive …
despite treatment, a small fraction (5–10%) of DCIS patients develop subsequent invasive …
[PDF][PDF] Mutations in REEP6 cause autosomal-recessive retinitis pigmentosa
Retinitis pigmentosa (RP) is the most frequent form of inherited retinal dystrophy. RP is
genetically heterogeneous and the genes identified to date encode proteins involved in a …
genetically heterogeneous and the genes identified to date encode proteins involved in a …
[HTML][HTML] Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients
J Salvo, V Lyubasyuk, M Xu, H Wang… - … & visual science, 2015 - jov.arvojournals.org
Purpose.: Familial exudative vitreoretinopathy (FEVR) is a developmental disease that can
cause visual impairment and retinal detachment at a young age. Four genes involved in the …
cause visual impairment and retinal detachment at a young age. Four genes involved in the …
Mutations in human IFT140 cause non-syndromic retinal degeneration
Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP) are two genetically
heterogeneous retinal degenerative disorders. Despite the identification of a number of …
heterogeneous retinal degenerative disorders. Despite the identification of a number of …
[PDF][PDF] Mutations in the spliceosome component CWC27 cause retinal degeneration with or without additional developmental anomalies
Pre-mRNA splicing factors play a fundamental role in regulating transcript diversity both
temporally and spatially. Genetic defects in several spliceosome components have been …
temporally and spatially. Genetic defects in several spliceosome components have been …
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
Malformations of cortical development (MCD) are neurological conditions involving focal
disruptions of cortical architecture and cellular organization that arise during …
disruptions of cortical architecture and cellular organization that arise during …
[HTML][HTML] Structure-function analysis reveals a novel mechanism for regulation of histone demethylase LSD2/AOF1/KDM1b
Abstract LSD2/AOF1/KDM1b catalyzes demethylation of mono-and di-methylated H3K4 and
plays an important role in transcriptional regulation and genomic imprinting. Here, we report …
plays an important role in transcriptional regulation and genomic imprinting. Here, we report …
Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing
G Kunde-Ramamoorthy, C Coarfa… - Nucleic acids …, 2014 - academic.oup.com
Coupling bisulfite conversion with next-generation sequencing (Bisulfite-seq) enables
genome-wide measurement of DNA methylation, but poses unique challenges for mapping …
genome-wide measurement of DNA methylation, but poses unique challenges for mapping …
[PDF][PDF] Spatially resolved transcriptomics of high-grade serous ovarian carcinoma
Bulk and single-cell RNA sequencing do not provide full characterization of tissue spatial
diversity in cancer samples, and currently available in situ techniques (multiplex …
diversity in cancer samples, and currently available in situ techniques (multiplex …