Cargando…

Neuronal Phenotype of col4a1 and col25a1: An Intriguing Hypothesis in Vertebrates Brain Aging

Collagens are the most abundant proteins in vertebrates and constitute the major components of the extracellular matrix. Collagens play an important and multifaceted role in the development and functioning of the nervous system and undergo structural remodeling and quantitative modifications during...

Descripción completa

Detalles Bibliográficos
Autores principales:	Leggieri, Adele, Attanasio, Chiara, Palladino, Antonio, de Girolamo, Paolo, Lucini, Carla, D’Angelo, Livia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836537/ https://www.ncbi.nlm.nih.gov/pubmed/35163698 http://dx.doi.org/10.3390/ijms23031778

Ejemplares similares

Cholinergic System and NGF Receptors: Insights from the Brain of the Short-Lived Fish Nothobranchius furzeri
por: de Girolamo, Paolo, et al.
Publicado: (2020)

Identification and Expression of Neurotrophin-6 in the Brain of Nothobranchius furzeri: One More Piece in Neurotrophin Research
por: Leggieri, Adele, et al.
Publicado: (2019)

Ontogenetic Pattern Changes of Nucleobindin-2/Nesfatin-1 in the Brain and Intestinal Bulb of the Short Lived African Turquoise Killifish
por: Montesano, Alessia, et al.
Publicado: (2019)

The Case Study of Nesfatin-1 in the Pancreas of Tursiops truncatus
por: Gatta, Claudia, et al.
Publicado: (2018)

Radiation increases COL1A1, COL3A1, and COL1A2 expression in breast cancer
por: Yao, Guorong, et al.
Publicado: (2022)

Differential Expression of COL1A1, COL1A2, COL6A3, and SULF1 as Prognostic Biomarkers in Gastric Cancer
por: Hu, Yan, et al.
Publicado: (2021)

Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations
por: Strafella, Claudia, et al.
Publicado: (2019)

Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1
por: Urbizu, Aintzane, et al.
Publicado: (2021)

Compound phenotype of osteogenesis imperfecta and Ehlers–Danlos syndrome caused by combined mutations in COL1A1 and COL5A1
por: Lin, Zejia, et al.
Publicado: (2019)

Mutations in COL1A1 and COL27A1 Associated with a Pectus Excavatum Phenotype in 2 Siblings with Osteogenesis Imperfecta
por: Cruz-Centeno, Nelimar, et al.
Publicado: (2022)

The Associations of Single Nucleotide Polymorphisms of the COL3A1, COL6A5, and COL8A1 Genes with Atopic Dermatitis
por: Szalus, Krzysztof, et al.
Publicado: (2023)

Identification of COL1A1 and COL1A2 as candidate prognostic factors in gastric cancer
por: Li, Jun, et al.
Publicado: (2016)

The impact of COL1A1 and COL6A1 expression on hypospadias and penile curvature severity
por: Yuri, Prahara, et al.
Publicado: (2020)

Central and Peripheral NPY Age-Related Regulation: A Comparative Analysis in Fish Translational Models
por: Giaquinto, Daniela, et al.
Publicado: (2022)

The correlation and role analysis of COL4A1 and COL4A2 in hepatocarcinogenesis
por: Liu, Yanli, et al.
Publicado: (2020)

Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome
por: Wang, Xun, et al.
Publicado: (2016)

Critical Early Roles for col27a1a and col27a1b in Zebrafish Notochord Morphogenesis, Vertebral Mineralization and Post-embryonic Axial Growth
por: Christiansen, Helena E., et al.
Publicado: (2009)

Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes
por: Zanotti, Simona, et al.
Publicado: (2023)

Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta
por: Ho Duy, Binh, et al.
Publicado: (2016)

Reviewing the Regulators of COL1A1
por: Devos, Hanne, et al.
Publicado: (2023)

Are COL4A1 and COL4A2 gene polymorphisms associated with cerebral palsy?
por: Güvener, Orhan, et al.
Publicado: (2021)

Main features of COL4A1-COL4A2 related cerebral microangiopathies
por: Guey, Stéphanie, et al.
Publicado: (2022)

Phenotypic characterization of patients with early-onset high myopia due to mutations in COL2A1 or COL11A1: Why not Stickler syndrome?
por: Zhou, Lin, et al.
Publicado: (2018)

Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum
por: Guo, Long, et al.
Publicado: (2017)

Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients
por: Zhytnik, Lidiia, et al.
Publicado: (2017)

Clinical significance of COL1A1 and COL1A2 expression levels in hypopharyngeal squamous cell carcinoma
por: Lin, Peiliang, et al.
Publicado: (2020)

The Phenotypic Spectrum of COL4A3 Heterozygotes
por: Solanki, Kaushal V., et al.
Publicado: (2023)

The Phenotypic Spectrum of COL4A3 Heterozygotes
por: Solanki, Kaushal V., et al.
Publicado: (2023)

COL25A1 triggers and promotes Alzheimer’s disease-like pathology in vivo
por: Tong, Ying, et al.
Publicado: (2009)

The Death of Col. Newcome
Publicado: (1953)

Lt.-Col. Maynard
Publicado: (1921)

So. Med. Col.
Publicado: (1889)

BDNF, Brain, and Regeneration: Insights from Zebrafish
por: Lucini, Carla, et al.
Publicado: (2018)

Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus
por: Karolak, Justyna A., et al.
Publicado: (2011)

Dietary Lecithin Decreases Skeletal Muscle COL1A1 and COL3A1 Gene Expression in Finisher Gilts
por: Akit, Henny, et al.
Publicado: (2016)

lnc-SAMD14-4 can regulate expression of the COL1A1 and COL1A2 in human chondrocytes
por: Zhang, Haibin, et al.
Publicado: (2019)

Genetic Polymorphisms of MMP1, MMP9, COL1A1, and COL1A2 in Polish Patients with Thoracic Aortopathy
por: Gorący, Iwona, et al.
Publicado: (2020)

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome
por: Liu, Jian-Hong, et al.
Publicado: (2017)

Modélo Col : análisis del supuesto epistemológico
por: Flores Alfonseca, Ma. Angélica
Publicado: (2004)

Rare Missense Functional Variants at COL4A1 and COL4A2 in Sporadic Intracerebral Hemorrhage
por: Chung, Jaeyoon, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_egpgai0c59vk6766sheitadvra