Cargando…

Publisher Correction: Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3

Detalles Bibliográficos
Autores principales:	Cova, Giulia, Glaser, Juliane, Schöpflin, Robert, Prada-Medina, Cesar Augusto, Ali, Salaheddine, Franke, Martin, Falcone, Rita, Federer, Miriam, Ponzi, Emanuela, Ficarella, Romina, Novara, Francesca, Wittler, Lars, Timmermann, Bernd, Gentile, Mattia, Zuffardi, Orsetta, Spielmann, Malte, Mundlos, Stefan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2023
Materias:	Publisher Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195858/ https://www.ncbi.nlm.nih.gov/pubmed/37202388 http://dx.doi.org/10.1038/s41467-023-38736-7

Ejemplares similares

Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3
por: Cova, Giulia, et al.
Publicado: (2023)

Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice
por: Hernandez-Miranda, Luis Rodrigo, et al.
Publicado: (2018)

Comparative genomics of Lbx loci reveals conservation of identical Lbx ohnologs in bony vertebrates
por: Wotton, Karl R, et al.
Publicado: (2008)

A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy
por: Caretto, Amelia, et al.
Publicado: (2014)

Lbx2 regulates formation of myofibrils
por: Ochi, Haruki, et al.
Publicado: (2009)

LBX2-AS1 as a Novel Diagnostic Biomarker and Therapeutic Target Facilitates Multiple Myeloma Progression by Enhancing mRNA Stability of LBX2
por: Jia, Haipeng, et al.
Publicado: (2021)

Role of Zebrafish Lbx2 in Embryonic Lateral Line Development
por: Chen, Xiaowen, et al.
Publicado: (2011)

MECP2 duplication phenotype in symptomatic females: report of three further cases
por: Novara, Francesca, et al.
Publicado: (2014)

Correction: Role of Zebrafish Lbx2 in Embryonic Lateral Line Development
por: Chen, Xiaowen, et al.
Publicado: (2012)

Identification of LBX2 as a novel causal gene of lung adenocarcinoma
por: Hu, Jingwen, et al.
Publicado: (2020)

The Susceptibility and Potential Functions of the LBX1 Gene in Adolescent Idiopathic Scoliosis
por: Luo, Ming, et al.
Publicado: (2021)

Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature
por: Errichiello, Edoardo, et al.
Publicado: (2016)

Overexpression of LBX2 associated with tumor progression and poor prognosis in colorectal cancer
por: Huang, Xiaodong, et al.
Publicado: (2020)

Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood
por: Novara, Francesca, et al.
Publicado: (2009)

Transcription Factor Lbx1 Expression in Mouse Embryonic Stem Cell-Derived Phenotypes
por: Schmitteckert, Stefanie, et al.
Publicado: (2011)

Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the Proliferation of Colorectal Cancer
por: Li, Qing, et al.
Publicado: (2021)

Genomic dissection of enhancers uncovers principles of combinatorial regulation and cell type-specific wiring of enhancer–promoter contacts
por: Thormann, Verena, et al.
Publicado: (2018)

Genomic dissection of enhancers uncovers principles of combinatorial regulation and cell type-specific wiring of enhancer–promoter contacts
por: Thormann, Verena, et al.
Publicado: (2018)

Haplotypes at LBX1 Have Distinct Inheritance Patterns with Opposite Effects in Adolescent Idiopathic Scoliosis
por: Chettier, Rakesh, et al.
Publicado: (2015)

Complete Genome Sequence and Characterization of a Polyethylene Biodegradation Strain, Streptomyces Albogriseolus LBX-2
por: Shao, Huanhuan, et al.
Publicado: (2019)

LncRNA LBX2-AS1 promotes colorectal cancer progression and 5-fluorouracil resistance
por: Ma, Yu-Nan, et al.
Publicado: (2021)

The role of LncRNA LBX2-AS1 in cancers: functions, mechanisms and potential clinical utility
por: Su, Yuanshuai, et al.
Publicado: (2022)

Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding
por: Andrey, Guillaume, et al.
Publicado: (2017)

Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome
por: Bonaglia, Maria Clara, et al.
Publicado: (2020)

Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes
por: Schöpflin, Robert, et al.
Publicado: (2022)

Association between Common Variants near LBX1 and Adolescent Idiopathic Scoliosis Replicated in the Chinese Han Population
por: Gao, Wenjie, et al.
Publicado: (2013)

Population-Specific Regulation of Chmp2b by Lbx1 during Onset of Synaptogenesis in Lateral Association Interneurons
por: Xu, Jun, et al.
Publicado: (2012)

Retraction Note: LncRNA LBX2-AS1 promotes colorectal cancer progression and 5-fluorouracil resistance
por: Ma, Yu-Nan, et al.
Publicado: (2023)

A newborn with ambiguous genitalia and a complex X;Y rearrangement
por: Dehghani, Mohammadreza, et al.
Publicado: (2014)

Phenotypic Expansion in Nasu-Hakola Disease: Immunological Findings in Three Patients and Proposal of a Unifying Pathogenic Hypothesis
por: Errichiello, Edoardo, et al.
Publicado: (2019)

RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism
por: Errichiello, Edoardo, et al.
Publicado: (2020)

In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients
por: Lucarelli, Enrico, et al.
Publicado: (2014)

Associations of LBX1 gene and adolescent idiopathic scoliosis susceptibility: a meta-analysis based on 34,626 subjects
por: Cao, Yaqin, et al.
Publicado: (2016)

Association of LBX1 Gene Methylation Level with Disease Severity in Patients with Idiopathic Scoliosis: Study on Deep Paravertebral Muscles
por: Janusz, Piotr, et al.
Publicado: (2022)

Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model
por: Mignogna, Maria Lidia, et al.
Publicado: (2021)

Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force
por: Rinaldi, Berardo, et al.
Publicado: (2017)

A Functional SNP in the Promoter of LBX1 Is Associated With the Development of Adolescent Idiopathic Scoliosis Through Involvement in the Myogenesis of Paraspinal Muscles
por: Xu, Leilei, et al.
Publicado: (2021)

Combinatorial targeting of FGF and ErbB receptors blocks growth and metastatic spread of breast cancer models
por: Issa, Amine, et al.
Publicado: (2013)

Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation
por: Melo, Uirá Souto, et al.
Publicado: (2023)

Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation
por: Melo, Uirá Souto, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_d3ajni2jpjo438or48u21j092u