4.7 Article

Autophagy Plays a Crucial Role in Ameloblast Differentiation

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Biochemistry & Molecular Biology

Impaired GATE16-mediated exocytosis in exocrine tissues causes Sjogren's syndrome-like exocrinopathy

Akiko Suzuki et al.

Summary: Sjogren's syndrome is a chronic autoimmune disease characterized by immune cell infiltration of the exocrine glands. Deficiency in enzymes involved in the ubiquitin modification pathway leads to a Sjogren's syndrome-like phenotype, and activation of GATE16 is crucial for exocytosis.

CELLULAR AND MOLECULAR LIFE SCIENCES (2022)

Article Multidisciplinary Sciences

Micro-computed tomography assessment of bone structure in aging mice

Junbo Shim et al.

Summary: In this study, a morphometric assessment of craniofacial bones was conducted in aging mice, and it was found that the microarchitecture of craniofacial bones is uniquely affected by age and sex. The interparietal bone and body of the mandible were less affected by age and sex, while the condyle of the mandible showed more pronounced changes in males compared to females.

SCIENTIFIC REPORTS (2022)

Article Genetics & Heredity

Crucial Roles of microRNA-16-5p and microRNA-27b-3p in Ameloblast Differentiation Through Regulation of Genes Associated With Amelogenesis Imperfecta

Akiko Suzuki et al.

Summary: This study reveals the regulatory network of genes and microRNAs (miRNAs) related to amelogenesis imperfecta. miR-16-5p and miR-27b-3p were identified as potential pathogenic miRNAs, as they significantly inhibited ameloblast differentiation by regulating mAIGenes.

FRONTIERS IN GENETICS (2022)

Review Cell Biology

Autophagy in the Regulation of Tissue Differentiation and Homeostasis

Cristiana Perrotta et al.

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)

Review Cell Biology

Mechanism and medical implications of mammalian autophagy

Ivan Dikic et al.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2018)

Article Endocrinology & Metabolism

DLX3-Dependent Regulation of Ion Transporters and Carbonic Anhydrases Is Crucial for Enamel Mineralization

Olivier Duverger et al.

JOURNAL OF BONE AND MINERAL RESEARCH (2017)

Review Physiology

DENTAL ENAMEL FORMATION AND IMPLICATIONS FOR ORAL HEALTH AND DISEASE

Rodrigo S. Lacruz et al.

PHYSIOLOGICAL REVIEWS (2017)

Review Cell Biology

Autophagy regulation by nutrient signaling

Ryan C. Russell et al.

CELL RESEARCH (2014)

Article Pharmacology & Pharmacy

The Nrf2 cell defence pathway: Keap1-dependent and -independent mechanisms of regulation

Holly K. Bryan et al.

BIOCHEMICAL PHARMACOLOGY (2013)

Article Multidisciplinary Sciences

Keap1 degradation by autophagy for the maintenance of redox homeostasis

Keiko Taguchi et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)

Review Biochemistry & Molecular Biology

Autophagy: Renovation of Cells and Tissues

Noboru Mizushima et al.

Article Genetics & Heredity

Genetic basis for tooth malformations: from mice to men and back again

T. A. Mitsiadis et al.

CLINICAL GENETICS (2011)

Article Biochemistry & Molecular Biology

Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega

Fabian Sievers et al.

MOLECULAR SYSTEMS BIOLOGY (2011)

Article Genetics & Heredity

Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome

Francesco Brancati et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2010)

Article Biochemistry & Molecular Biology

The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice

Martin J. Barron et al.

HUMAN MOLECULAR GENETICS (2008)

Review Genetics & Heredity

Amelogenesis imperfecta

Peter J. M. Crawford et al.

ORPHANET JOURNAL OF RARE DISEASES (2007)

Article Cell Biology

Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice

M Komatsu et al.

JOURNAL OF CELL BIOLOGY (2005)

Article Genetics & Heredity

DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism

J Dong et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)

Article Genetics & Heredity

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

PS Hart et al.

JOURNAL OF MEDICAL GENETICS (2004)

Article Dentistry, Oral Surgery & Medicine

Amelogenesis imperfecta: a classification and catalogue for the 21st century

MJ Aldred et al.

ORAL DISEASES (2003)