Cargando…

Establishment of DNA methylation patterns of the Fibrillin1 (FBN1) gene in porcine embryos and tissues

DNA methylation in transcriptional regulatory regions is crucial for gene expression. The DNA methylation status of the edges of CpG islands, called CpG island shore, is involved in tissue/cell-type-specific gene expression. Haploinsufficiency diseases are caused by inheritance of one mutated null a...

Descripción completa

Detalles Bibliográficos
Autores principales:	ARAI, Yoshikazu, UMEYAMA, Kazuhiro, TAKEUCHI, Kenta, OKAZAKI, Natsumi, HICHIWA, Naomi, YASHIMA, Sayaka, NAKANO, Kazuaki, NAGASHIMA, Hiroshi, OHGANE, Jun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Society for Reproduction and Development 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401809/ https://www.ncbi.nlm.nih.gov/pubmed/28111381 http://dx.doi.org/10.1262/jrd.2016-158

Ejemplares similares

DNA methylation ambiguity in the Fibrillin-1 (FBN1) CpG island shore possibly involved in Marfan syndrome
por: Arai, Yoshikazu, et al.
Publicado: (2020)

Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
por: Cierna, Z., et al.
Publicado: (2016)

DNA methylation profiles provide a viable index for porcine pluripotent stem cells
por: Arai, Yoshikazu, et al.
Publicado: (2013)

Generation of heterozygous fibrillin-1 mutant cloned pigs from genome-edited foetal fibroblasts
por: Umeyama, Kazuhiro, et al.
Publicado: (2016)

Generating Porcine Chimeras Using Inner Cell Mass Cells and Parthenogenetic Preimplantation Embryos
por: Nakano, Kazuaki, et al.
Publicado: (2013)

Intravitreal injection of fibrillin 2 (Fbn2) recombinant protein for therapy of retinopathy in a retina-specific Fbn2 knock-down mouse model
por: Zhang, Rui Xue, et al.
Publicado: (2023)

FBN-1, a fibrillin-related protein, is required for resistance of the epidermis to mechanical deformation during C. elegans embryogenesis
por: Kelley, Melissa, et al.
Publicado: (2015)

Genome-wide identification and expression analysis of fibrillin (FBN) gene family in tomato (Solanum lycopersicum L.)
por: Sun, Huiru, et al.
Publicado: (2022)

Author Correction: Intravitreal injection of fibrillin 2 (Fbn2) recombinant protein for therapy of retinopathy in a retina-specific Fbn2 knock-down mouse model
por: Zhang, Rui Xue, et al.
Publicado: (2023)

A transgenic-cloned pig model expressing non-fluorescent modified Plum
por: NAGAYA, Masaki, et al.
Publicado: (2016)

Genome-Wide Characterization and Sequence Polymorphism Analyses of Glycine max Fibrillin (FBN) Revealed Its Role in Response to Drought Condition
por: Zafer, Muhammad Zeshan, et al.
Publicado: (2023)

Anephrogenic phenotype induced by SALL1 gene knockout in pigs
por: Watanabe, Masahito, et al.
Publicado: (2019)

De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation
por: Wang, Shuling, et al.
Publicado: (2017)

Generation of α1,3-galactosyltransferase and cytidine monophospho-N-acetylneuraminic acid hydroxylase gene double-knockout pigs
por: MIYAGAWA, Shuji, et al.
Publicado: (2015)

Microenvironmental Regulation by Fibrillin-1
por: Sengle, Gerhard, et al.
Publicado: (2012)

Distributions of endocrine cell clusters during porcine pancreatic development
por: Nagaya, Masaki, et al.
Publicado: (2019)

Application of hollow fiber vitrification for cryopreservation of bovine early cleavage stage embryos and porcine morula-blastomeres
por: UCHIKURA, Ayuko, et al.
Publicado: (2016)

Genetically engineered animal models for Marfan syndrome: challenges associated with the generation of pig models for diseases caused by haploinsufficiency
por: JACK, Naomi, et al.
Publicado: (2022)

Fibrillin-1 regulates periostin expression during maintenance of periodontal homeostasis
por: Yoshikazu Manabe, et al.
Publicado: (2022)

Fibrillins in Tendon
por: Giusti, Betti, et al.
Publicado: (2016)

The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2
por: Peeters, Silke, et al.
Publicado: (2022)

Fibrillin-1 regulates the bioavailability of TGFβ1
por: Chaudhry, Shazia S., et al.
Publicado: (2007)

Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos
por: Zeng, Yanting, et al.
Publicado: (2018)

Fibrillin-1 Regulates Arteriole Integrity in the Retina
por: Alonso, Florian, et al.
Publicado: (2022)

The Effect of Ultraviolet B on Fibrillin-1 and Fibrillin-2 in Human Non-pigmented Ciliary Epithelial Cells In Vitro
por: Shiroto, Yuki, et al.
Publicado: (2017)

POGLUT2 and POGLUT3 O-glucosylate multiple EGF repeats in fibrillin-1, -2, and LTBP1 and promote secretion of fibrillin-1
por: Williamson, Daniel B., et al.
Publicado: (2021)

A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome
por: Torrado, Mario, et al.
Publicado: (2018)

Phenotypic features of genetically modified DMD-X(KO)X(WT) pigs
por: Okamoto, Kazutoshi, et al.
Publicado: (2023)

Matrix Metalloproteinase-2 Degrades Fibrillin-1 and Fibrillin-2 of Oxytalan Fibers in the Human Eye and Periodontal Ligaments In Vitro
por: Kawagoe, Megumi, et al.
Publicado: (2013)

The Multiple Functions of Fibrillin-1 Microfibrils in Organismal Physiology
por: Asano, Keiichi, et al.
Publicado: (2022)

Fibrillin-1 regulates endothelial sprouting during angiogenesis
por: Alonso, Florian, et al.
Publicado: (2023)

Ultra-Deep Bisulfite Sequencing to Detect Specific DNA Methylation Patterns of Minor Cell Types in Heterogeneous Cell Populations: An Example of the Pituitary Tissue
por: Arai, Yoshikazu, et al.
Publicado: (2016)

Identification of gross deletions in FBN1 gene by MLPA
por: Yang, Hang, et al.
Publicado: (2018)

Molecular cloning, characterization and 3D modelling of spotted snakehead fbn1 C-terminal region encoding asprosin and expression analysis of fbn1
por: Sathoria, Priyanka, et al.
Publicado: (2023)

Multi-exon deletions of the FBN1 gene in Marfan syndrome
por: Liu, Wanguo, et al.
Publicado: (2001)

Identification of novel FBN1 variations implicated in congenital scoliosis
por: Lin, Mao, et al.
Publicado: (2019)

The Supramolecular Organization of Fibrillin-Rich Microfibrils
por: Baldock, Clair, et al.
Publicado: (2001)

The Evolution of Extracellular Fibrillins and Their Functional Domains
por: Piha-Gossack, Adam, et al.
Publicado: (2012)

Fibrillin Microfibrils Keep the Cornea in Shape
por: Chakravarti, Shukti
Publicado: (2017)

Aortic Strain Correlates With Elastin Fragmentation in Fibrillin-1 Hypomorphic Mice
por: Chen, Jeff Z., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_jq7lgcleq6skvbkroh70gnh783