Lista de obras - Ivan Duran - Dominio Público Uruguay

A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen

artículo científico publicado en 2017

Actinotrichia collagens and their role in fin formation ⬇️

artículo científico publicado el 17 de marzo de 2011

Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

artículo científico publicado en 2016

An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome.

artículo científico publicado en 2016

Collagen duplicate genes of bone and cartilage participate during regeneration of zebrafish fin skeleton

artículo científico publicado en 2015

Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

artículo científico publicado en 2016

Corrigendum: The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery.

artículo científico publicado en 2016

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome

artículo científico publicado en 2016

Dominant-negative SOX9 mutations in campomelic dysplasia

artículo científico publicado en 2019

Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies.

artículo científico publicado en 2017

Fibroblast growth factor and canonical WNT/β-catenin signaling cooperate in suppression of chondrocyte differentiation in experimental models of FGFR signaling in cartilage.

artículo científico publicado en 2015

Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase

artículo científico publicado en 2019

Freeze substitution followed by low melting point wax embedding preserves histomorphology and allows protein and mRNA localization techniques

artículo científico publicado en 2010

HSP47 and FKBP65 cooperate in the synthesis of type I procollagen.

artículo científico publicado en 2014

Holmgren's principle of delamination during fin skeletogenesis

artículo científico publicado en 2014

Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome

scientific journal article

Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia.

scientific article published on 10 April 2017

NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot

artículo científico publicado en 2018

Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio.

artículo científico publicado en 2007

Ray-interray interactions during fin regeneration of Danio rerio.

artículo científico publicado en 2002

Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathies.

artículo científico publicado en 2018

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

artículo científico publicado en 2016

The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling

artículo científico publicado en 2018

The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery

artículo científico publicado en 2016

The α2 chain of type IX collagen is essential for type IX collagen biosynthesis

scientific article published on 03 June 2019

Lista de obras de Ivan Duran

A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen

Actinotrichia collagens and their role in fin formation ⬇️

Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome.

Collagen duplicate genes of bone and cartilage participate during regeneration of zebrafish fin skeleton

Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

Corrigendum: The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery.

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome

Dominant-negative SOX9 mutations in campomelic dysplasia

Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies.

Fibroblast growth factor and canonical WNT/β-catenin signaling cooperate in suppression of chondrocyte differentiation in experimental models of FGFR signaling in cartilage.

Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase

Freeze substitution followed by low melting point wax embedding preserves histomorphology and allows protein and mRNA localization techniques

HSP47 and FKBP65 cooperate in the synthesis of type I procollagen.

Holmgren's principle of delamination during fin skeletogenesis

Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome

Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia.

NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot

Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio.

Ray-interray interactions during fin regeneration of Danio rerio.

Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathies.

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling

The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery

The α2 chain of type IX collagen is essential for type IX collagen biosynthesis