Cargando…

Regional Selection Acting on the OFD1 Gene Family

The OFD1 (oral-facial-digital, type 1) gene is implicated in several developmental disorders in humans. The X-linked OFD1 (OFD1X) is conserved in Eutheria. Knowledge about the Y-linked paralog (OFD1Y) is limited. In this study, we identified an OFD1Y on the bovine Y chromosome, which is expressed di...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chang, Ti-Cheng, Klabnik, Jessica L., Liu, Wan-Sheng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193505/ https://www.ncbi.nlm.nih.gov/pubmed/22022562 http://dx.doi.org/10.1371/journal.pone.0026195

Ejemplares similares

OFD1 : One gene, several disorders
por: Pezzella, Nunziana, et al.
Publicado: (2022)

A novel non-sense variant in the OFD1 gene caused Joubert syndrome
por: Li, Chen, et al.
Publicado: (2023)

Pensionen aus der Schweiz steuerpflichtig (OFD)
Publicado: (2009)

Update on oral-facial-digital syndromes (OFDS)
por: Franco, Brunella, et al.
Publicado: (2016)

Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome
por: Papuc, Sorina Mihaela, et al.
Publicado: (2023)

A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report
por: DEHGHAN TEZERJANI, Masoud, et al.
Publicado: (2016)

The OFD1 protein is a novel player in selective autophagy: another tile to the cilia/autophagy puzzle
por: Morleo, Manuela, et al.
Publicado: (2021)

CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study
por: Del Giudice, Ennio, et al.
Publicado: (2014)

Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia
por: Yang, Binyi, et al.
Publicado: (2022)

IK is essentially involved in ciliogenesis as an upstream regulator of oral-facial-digital syndrome ciliopathy gene, ofd1
por: Ka, Hye In, et al.
Publicado: (2023)

OFD1, as a Ciliary Protein, Exhibits Neuroprotective Function in Photoreceptor Degeneration Models
por: Wang, Juan, et al.
Publicado: (2016)

Autophagy Promotes Primary Ciliogenesis by Removing OFD1 from Centriolar Satellites
por: Tang, Zaiming, et al.
Publicado: (2013)

Abnormal accumulation of OFD1 in endometrial cancer with poor prognosis inhibits ciliogenesis
por: Kojima, Ryuji, et al.
Publicado: (2022)

The Relationship Between Human Papillomavirus, OFD1 and Primary Ciliogenesis in the Progression of Oropharyngeal Cancer: A Retrospective Cohort Study
por: Meng, Hong-xue, et al.
Publicado: (2020)

The S. pombe Histone H2A Dioxygenase Ofd2 Regulates Gene Expression during Hypoxia
por: Lando, David, et al.
Publicado: (2012)

Ofd1 Controls Dorso-Ventral Patterning and Axoneme Elongation during Embryonic Brain Development
por: D'Angelo, Anna, et al.
Publicado: (2012)

What drives product involvement and satisfaction with OFDs amid COVID-19?
por: Das, Manoj, et al.
Publicado: (2022)

OFD1 and VFL3/CCDC61 in basal body positioning and docking in Paramecium
por: Bengueddach, H, et al.
Publicado: (2015)

The centrosomal OFD1 protein interacts with the translation machinery and regulates the synthesis of specific targets
por: Iaconis, Daniela, et al.
Publicado: (2017)

Distinct Roles of TRAPPC8 and TRAPPC12 in Ciliogenesis via Their Interactions With OFD1
por: Zhang, Caiyun, et al.
Publicado: (2020)

Myosin VI regulates ciliogenesis by promoting the turnover of the centrosomal/satellite protein OFD1
por: Magistrati, Elisa, et al.
Publicado: (2021)

Basal body positioning and anchoring in the multiciliated cell Paramecium tetraurelia: roles of OFD1 and VFL3
por: Bengueddach, Hakim, et al.
Publicado: (2017)

Retinitis Pigmentosa and Bilateral Idiopathic Demyelinating Optic Neuritis in a 6-Year-Old Boy with OFD1 Gene Mutation
por: Wang, Xun, et al.
Publicado: (2017)

Somatic mutations in GLI3 and OFD1 involved in sonic hedgehog signaling cause hypothalamic hamartoma
por: Saitsu, Hirotomo, et al.
Publicado: (2016)

The Expansion of the PRAME Gene Family in Eutheria
por: Chang, Ti-Cheng, et al.
Publicado: (2011)

Regulation of SREBP during hypoxia requires Ofd1-mediated control of both DNA bindingand degradation
por: Porter, Joshua R., et al.
Publicado: (2012)

MARK4 contributes to cilia formation by regulating the degradation of inhibitory OFD1 from the centriolar satellites
por: Carvalho, R, et al.
Publicado: (2015)

MfOfd1 is crucial for stress responses and virulence in the peach brown rot fungus Monilinia fructicola
por: Zhang, Ming-Ming, et al.
Publicado: (2020)

OFD1 and Flotillins Are Integral Components of a Ciliary Signaling Protein Complex Organized by Polycystins in Renal Epithelia and Odontoblasts
por: Jerman, Stephanie, et al.
Publicado: (2014)

The evolutionary conserved proteins CEP90, FOPNL, and OFD1 recruit centriolar distal appendage proteins to initiate their assembly
por: Le Borgne, Pierrick, et al.
Publicado: (2022)

Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene
por: Ferrante, Maria I., et al.
Publicado: (2009)

Schizosaccharomyces pombe Ofd2 Is a Nuclear 2-Oxoglutarate and Iron Dependent Dioxygenase Interacting with Histones
por: Korvald, Hanne, et al.
Publicado: (2011)

The expanding phenotype of OFD1‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia
por: Hannah, William B., et al.
Publicado: (2019)

Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1
por: Linpeng, Siyuan, et al.
Publicado: (2018)

The TBC1D31/praja2 complex controls primary ciliogenesis through PKA‐directed OFD1 ubiquitylation
por: Senatore, Emanuela, et al.
Publicado: (2021)

Recruitment of FOR20 and OFD1 onto pericentriolar satellites and centrosomes depends on the formation of a ternary complex with KIAA0753
por: Chevrier, V, et al.
Publicado: (2015)

OFD1 mutation induced renal failure and polycystic kidney disease in a pair of childhood male twins in China
por: Zhang, Hong-Wen, et al.
Publicado: (2020)

Pension finance: putting the risks and costs ofd defined benefit plans back under your control
por: Waring, M. Barton, et al.
Publicado: (2011)

An Orofaciodigital Syndrome 1 Patient and Her Mother Carry the Same OFD1 Mutation but Have Different X Chromosome Inactivation Patterns
por: Iijima, Takashi, et al.
Publicado: (2019)

Exome sequencing identifies a mutation in OFD1 in a male with Joubert syndrome, orofaciodigital spectrum anomalies and complex polydactyly
por: Wentzensen, Ingrid M, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_5he0sma92njk63ki54hdqst474