Cargando…

Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish

H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development as it is widely expressed in the eye, peripheral ganglia and branchial arches. Mutations in HMX1 are linked to an ocular defect termed Oculo-auricular syndrome of Schorderet-Munier-Franceschetti (MIM #612109). We iden...

Descripción completa

Detalles Bibliográficos
Autores principales:	El Fersioui, Younes, Pinton, Gaëtan, Allaman-Pillet, Nathalie, Schorderet, Daniel F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815118/ https://www.ncbi.nlm.nih.gov/pubmed/33465110 http://dx.doi.org/10.1371/journal.pone.0245239

Ejemplares similares

Premature Vertebral Mineralization in hmx1-Mutant Zebrafish
por: El Fersioui, Younes, et al.
Publicado: (2022)

A Dimerized HMX1 Inhibits EPHA6/epha4b in Mouse and Zebrafish Retinas
por: Marcelli, Fabienne, et al.
Publicado: (2014)

Piperlongumine promotes death of retinoblastoma cancer cells
por: Allaman-Pillet, Nathalie, et al.
Publicado: (2021)

Identification of HMX1 target genes: A predictive promoter model approach
por: Boulling, Arnaud, et al.
Publicado: (2013)

Bigh3 silencing increases retinoblastoma tumor growth in the murine SV40-TAg-Rb model
por: Allaman-Pillet, Nathalie, et al.
Publicado: (2017)

Preparation of Spherical HMX/DMF Solvates, Spherical HMX Particles, and HMX@NTO Composites: A Way to Reduce the Sensitivity of HMX
por: Zhao, Huipeng, et al.
Publicado: (2023)

Anteroposterior patterning of the zebrafish ear through Fgf- and Hh-dependent regulation of hmx3a expression
por: Hartwell, Ryan D., et al.
Publicado: (2019)

Incomplete Recovery of Zebrafish Retina Following Cryoinjury
por: Džulová, Denisa, et al.
Publicado: (2022)

Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation
por: Quina, Lely A., et al.
Publicado: (2012)

Identifying mutations in Tunisian families with retinal dystrophy
por: Habibi, Imen, et al.
Publicado: (2016)

Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy
por: Habibi, Imen, et al.
Publicado: (2017)

Aberrant expression of NKL homeobox genes HMX2 and HMX3 interferes with cell differentiation in acute myeloid leukemia
por: Nagel, Stefan, et al.
Publicado: (2020)

Mechanical properties of β-HMX
por: Gallagher, Hugh G, et al.
Publicado: (2015)

Molecular dynamic insight into octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) and the nano-HMX decomposition mechanism
por: Zhou, Mingming, et al.
Publicado: (2022)

Analyses of binding partners and functional domains for the developmentally essential protein Hmx3a/HMX3
por: Haws, William, et al.
Publicado: (2023)

Biofunctionalization of HMX with Peptides via Polydopamine Crosslinking for Assembling an HMX@Al@CuO Nanoenergetic Composite
por: Jin, Miaomiao, et al.
Publicado: (2023)

Requiem K. 626, hmx2901620/
por: Amadeus Mozart, Wolfgang

Growth and dislocation studies of β-HMX
por: Gallagher, Hugh G, et al.
Publicado: (2014)

Expression and Functional Analysis of cofilin1-like in Craniofacial Development in Zebrafish
por: Jin, Sil, et al.
Publicado: (2022)

Hmx3a Has Essential Functions in Zebrafish Spinal Cord, Ear and Lateral Line Development
por: England, Samantha J., et al.
Publicado: (2020)

vwa1 Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway
por: Niu, Xiaomin, et al.
Publicado: (2023)

New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family
por: Vaclavik, Veronika, et al.
Publicado: (2022)

Theoretical Studies on the Performance of HMX with Different Energetic Groups
por: Hao, Lina, et al.
Publicado: (2020)

Duplication in ECR near HMX1 and a SNP in GATA6 Genes Regulate Microtia in Awassi Sheep
por: Jawasreh, Khaleel I. Z., et al.
Publicado: (2020)

Mosmo Is Required for Zebrafish Craniofacial Formation
por: Camacho-Macorra, Carlos, et al.
Publicado: (2021)

Vitamin D Receptor Signaling Regulates Craniofacial Cartilage Development in Zebrafish
por: Kwon, Hye-Joo
Publicado: (2019)

Involvement of the zebrafish trrap gene in craniofacial development
por: Suzuki, Taichi, et al.
Publicado: (2021)

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass
por: Munroe, Robert J, et al.
Publicado: (2009)

A Non-Coding Genomic Duplication at the HMX1 Locus Is Associated with Crop Ears in Highland Cattle
por: Koch, Caroline Tina, et al.
Publicado: (2013)

Mutation analysis of Netrin 1 and HMX3 genes in patients with superior semicircular canal dehiscence syndrome
por: Roknic, Nikola, et al.
Publicado: (2012)

Study on the Effect of NTO on the Performance of HMX-Based Aluminized Cast-PBX
por: Nie, Pengsong, et al.
Publicado: (2022)

Size, Morphology and Crystallinity Control Strategy of Ultrafine HMX by Microfluidic Platform
por: Jiang, Hanyu, et al.
Publicado: (2023)

Osteomas of the craniofacial region
por: Nah, Kyung-Soo
Publicado: (2011)

Zebrafish Models of Craniofacial Malformations: Interactions of Environmental Factors
por: Raterman, S. T., et al.
Publicado: (2020)

Riboceine Rescues Auranofin-Induced Craniofacial Defects in Zebrafish
por: Leask, Megan, et al.
Publicado: (2021)

Zebrafish as an experimental model for the simulation of neurological and craniofacial disorders
por: Rai, Ashwin Rohan, et al.
Publicado: (2022)

High‐throughput detection of craniofacial defects in fluorescent zebrafish
por: Everson, Joshua L., et al.
Publicado: (2022)

Disruption of fos causes craniofacial anomalies in developing zebrafish
por: Maili, Lorena, et al.
Publicado: (2023)

Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia
por: Si, Nuo, et al.
Publicado: (2020)

Investigation of the solid–liquid ternary phase diagrams of 2HNIW·HMX cocrystal
por: Jia, Qian, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_0jbb7j8fhqd51u7di2qnosmcss