Cargando…

Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing

Detalles Bibliográficos
Autores principales:	Wang, Xiaoyuan, Zhang, Yanqin, Ding, Jie, Wang, Fang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2021
Materias:	Author Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578218/ https://www.ncbi.nlm.nih.gov/pubmed/34754083 http://dx.doi.org/10.1038/s41598-021-01604-9

Ejemplares similares

mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing
por: Wang, Xiaoyuan, et al.
Publicado: (2021)

Pathogenic variants of Alport syndrome and monogenic diabetes identified by exome sequencing in a family
por: Watanabe, Hirofumi, et al.
Publicado: (2023)

Compound Heterozygous Missense and Deep Intronic Variants in NDUFAF6 Unraveled by Exome Sequencing and mRNA Analysis
por: Catania, Alessia, et al.
Publicado: (2018)

Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
por: Wang, Qingbo, et al.
Publicado: (2021)

Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon
por: Mathur, Praveen, et al.
Publicado: (2018)

Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
por: Wilcox, Naomi, et al.
Publicado: (2023)

Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
por: Oh, Jong Jin, et al.
Publicado: (2020)

Author Correction: Combinatorial immunotherapies overcome MYC-driven immune evasion in triple negative breast cancer
por: Lee, Joyce V., et al.
Publicado: (2022)

A deep intronic splice variant of the COL4A5 gene in a Chinese family with X-linked Alport syndrome
por: Qian, Pei, et al.
Publicado: (2023)

Intronic variants in inborn errors of metabolism: Beyond the exome
por: Hertzog, Ashley, et al.
Publicado: (2022)

Author Correction: Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients
por: Sohn, Minji, et al.
Publicado: (2020)

Author Correction: Visualizing group II intron dynamics between the first and second steps of splicing
por: Manigrasso, Jacopo, et al.
Publicado: (2022)

Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis
por: Chiereghin, Chiara, et al.
Publicado: (2017)

Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
por: Bailey, Matthew H., et al.
Publicado: (2020)

Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
por: Slavotinek, Anne, et al.
Publicado: (2023)

Author Correction: SCON—a Short Conditional intrON for conditional knockout with one-step zygote injection
por: Wu, Szu-Hsien Sam, et al.
Publicado: (2023)

Author Correction: Effectiveness of mRNA-1273 against SARS-CoV-2 Omicron and Delta variants
por: Tseng, Hung Fu, et al.
Publicado: (2022)

Author Correction: Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma
por: Hu, Xin, et al.
Publicado: (2021)

Author Correction: Deep-learning-based ghost imaging
por: Lyu, Meng, et al.
Publicado: (2018)

Author Correction: Resonant out-of-phase fluorescence microscopy and remote imaging overcome spectral limitations
por: Quérard, Jérôme, et al.
Publicado: (2017)

Author Correction: Overcoming NADPH product inhibition improves D-sorbitol conversion to L-sorbose
por: Kim, Tae-Su, et al.
Publicado: (2019)

Author Correction to: Rapid protein evolution, organellar reductions, and invasive intronic elements in the marine aerobic parasite dinoflagellate Amoebophrya spp
por: Farhat, Sarah, et al.
Publicado: (2021)

Author Correction: Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing
por: Kim, Hyunsuk, et al.
Publicado: (2020)

Author Correction: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data
por: Wright, C. F., et al.
Publicado: (2022)

Overcoming HLA restriction in clinical trials: Immune monitoring of mRNA-loaded DC therapy
por: Van Nuffel, An M.T., et al.
Publicado: (2012)

Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
por: Zhang, Li, et al.
Publicado: (2023)

Author Correction: Overcoming Bias: Cognitive Control Reduces Susceptibility to Framing Effects in Evaluating Musical Performance
por: Aydogan, Gökhan, et al.
Publicado: (2018)

Author Correction: Identification and characterization of SSE15206, a microtubule depolymerizing agent that overcomes multidrug resistance
por: Manzoor, Safia, et al.
Publicado: (2018)

Author Correction: Butein promotes ubiquitination-mediated survivin degradation inhibits tumor growth and overcomes chemoresistance
por: Dong, Xin, et al.
Publicado: (2023)

Author Correction: Androgen receptor and its splice variant, AR-V7, differentially induce mRNA splicing in prostate cancer cells
por: Rana, Manjul, et al.
Publicado: (2021)

X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
por: Zhang, Xiao, et al.
Publicado: (2018)

Author Correction: Deep sequencing reveals the first fabavirus infecting peach
por: He, Yan, et al.
Publicado: (2018)

Author Correction: A deep learning approach to identifying immunogold particles in electron microscopy images
por: Jerez, Diego, et al.
Publicado: (2021)

Author Correction: Facile single-stranded DNA sequencing of human plasma DNA via thermostable group II intron reverse transcriptase template switching
por: Wu, Douglas C., et al.
Publicado: (2018)

Author Correction: VAMPnets for deep learning of molecular kinetics
por: Mardt, Andreas, et al.
Publicado: (2018)

Author Correction: Development and performance of a targeted whole exome sequencing enrichment kit for the dog (Canis Familiaris Build 3.1)
por: Broeckx, Bart J. G., et al.
Publicado: (2020)

Author Correction: Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations
por: Jeong, Dajeong, et al.
Publicado: (2022)

Author Directory
Publicado: (2013)

Author Index
Publicado: (2013)

Effect of heterozygous pathogenic COL4A3 or COL4A4 variants on patients with X‐linked Alport syndrome
por: Zhang, Yanqin, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_a5mq4329m0g3f6tmparjd48s9q