Absence of TRIC-B from type XIV Osteogenesis Imperfecta osteoblasts alters cell adhesion and mitochondrial function - A multi-omics study.
暂无分享,去创建一个
A. Forlino | R. Besio | J. Marini | Apratim Mitra | Milena M. Jovanović | Ryan K. Dale | B. Contento | A. Derkyi | M. To | Ka-wai Wong | Alberta Derkyi
[1] M. Brini,et al. CaMKII inhibition due to TRIC-B loss-of-function dysregulates SMAD signalling in osteogenesis imperfecta. , 2023, Matrix biology : journal of the International Society for Matrix Biology.
[2] Satoru Otsuru,et al. ER, Mitochondria, and ISR Regulation by mt‐HSP70 and ATF5 upon Procollagen Misfolding in Osteoblasts , 2022, Advanced science.
[3] J. Garcia,et al. Essential role for paxillin tyrosine phosphorylation in LPS-induced mitochondrial fission, ROS generation and lung endothelial barrier loss , 2021, Scientific Reports.
[4] Xiaochen Bo,et al. clusterProfiler 4.0: A universal enrichment tool for interpreting omics data , 2021, Innovation.
[5] J. Marini,et al. Osteogenesis Imperfecta: Mechanisms and signaling pathways connecting classical and rare OI types. , 2021, Endocrine reviews.
[6] F. Rauch,et al. Muscle Transcriptome in mouse models of Osteogenesis Imperfecta. , 2021, Bone.
[7] M. Raspanti,et al. Targeting cellular stress in vitro improves osteoblast homeostasis, matrix collagen content and mineralization in two murine models of osteogenesis imperfecta. , 2021, Matrix biology : journal of the International Society for Matrix Biology.
[8] E. Peles,et al. Differential Contribution of Cadm1–Cadm3 Cell Adhesion Molecules to Peripheral Myelinated Axons , 2021, The Journal of Neuroscience.
[9] Jean-Charles Sanchez,et al. Intracellular and Extracellular Markers of Lethality in Osteogenesis Imperfecta: A Quantitative Proteomic Approach , 2021, International journal of molecular sciences.
[10] E. Seuntjens,et al. Protocadherins at the Crossroad of Signaling Pathways , 2020, Frontiers in Molecular Neuroscience.
[11] P. Thistlethwaite,et al. Notch Enhances Ca2+ Entry by Activating Calcium-sensing Receptors and Inhibiting Voltage-gated K+ Channels. , 2020, American journal of physiology. Cell physiology.
[12] L. Lackner,et al. Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology , 2020, The Journal of cell biology.
[13] W. Prinz,et al. The functional universe of membrane contact sites , 2019, Nature Reviews Molecular Cell Biology.
[14] R. Rector,et al. Compromised Exercise Capacity and Mitochondrial Dysfunction in the Osteogenesis Imperfecta Murine (oim) Mouse Model , 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[15] X. Shang,et al. Notch Signaling in Osteogenesis, Osteoclastogenesis, and Angiogenesis. , 2019, The American journal of pathology.
[16] C. Chow,et al. Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes , 2019, The FEBS journal.
[17] A. Pitsillides,et al. Dchs1-Fat4 regulation of osteogenic differentiation in mouse , 2019, Development.
[18] Alireza Hadj Khodabakhshi,et al. Metascape provides a biologist-oriented resource for the analysis of systems-level datasets , 2019, Nature Communications.
[19] R. Morello,et al. The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis Imperfecta , 2019, JBMR plus.
[20] S. Ito,et al. Roles of the endoplasmic reticulum–resident, collagen-specific molecular chaperone Hsp47 in vertebrate cells and human disease , 2018, The Journal of Biological Chemistry.
[21] R. Mayor,et al. Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo , 2018, Nature Communications.
[22] R. Pulgar,et al. FR58P1a; a new uncoupler of OXPHOS that inhibits migration in triple-negative breast cancer cells via Sirt1/AMPK/β1-integrin pathway , 2018, Scientific Reports.
[23] J. Kere,et al. CELSR2 is a candidate susceptibility gene in idiopathic scoliosis , 2017, PloS one.
[24] Kris A. DeMali,et al. Interplay between tight junctions & adherens junctions , 2017, Experimental cell research.
[25] S. Stewart,et al. Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect , 2017, The Journal of clinical endocrinology and metabolism.
[26] Geet Duggal,et al. Salmon: fast and bias-aware quantification of transcript expression using dual-phase inference , 2017, Nature Methods.
[27] Trushar R. Patel,et al. LAR protein tyrosine phosphatase regulates focal adhesions through CDK1 , 2016, Journal of Cell Science.
[28] P. Várnai,et al. Redox Nanodomains Are Induced by and Control Calcium Signaling at the ER-Mitochondrial Interface. , 2016, Molecular cell.
[29] L. Ala‐Kokko,et al. Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta , 2016, PLoS genetics.
[30] E. Canalis,et al. Notch Signaling and the Skeleton. , 2016, Endocrine reviews.
[31] Asan,et al. Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta , 2016, Journal of Human Genetics.
[32] Matthew Stephens,et al. False discovery rates: a new deal , 2016, bioRxiv.
[33] R. Gioia,et al. Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfecta. , 2015, Human molecular genetics.
[34] M. Barbe,et al. Integrin Mediated Adhesion of Osteoblasts to Connective Tissue Growth Factor (CTGF/CCN2) Induces Cytoskeleton Reorganization and Cell Differentiation , 2015, PloS one.
[35] S. Mohan,et al. Differential Expression of Claudin Family Members during Osteoblast and Osteoclast Differentiation: Cldn-1 Is a Novel Positive Regulator of Osteoblastogenesis , 2014, PloS one.
[36] W. Huber,et al. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 , 2014, Genome Biology.
[37] R. Klein,et al. FLRT Structure: Balancing Repulsion and Cell Adhesion in Cortical and Vascular Development , 2014, Neuron.
[38] A. Morgan,et al. A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. , 2014, Gene.
[39] Sahar Mansour,et al. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development , 2013, Nature Genetics.
[40] M. Bouchard,et al. Inactivation of LAR family phosphatase genes Ptprs and Ptprf causes craniofacial malformations resembling Pierre-Robin sequence , 2013, Development.
[41] W. Shi,et al. The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote , 2013, Nucleic acids research.
[42] D. Landau,et al. A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta , 2013, Human mutation.
[43] R. Resende,et al. Nucleoplasmic calcium signaling and cell proliferation: calcium signaling in the nucleus , 2013, Cell Communication and Signaling.
[44] C. Hamanishi,et al. Cell adhesion molecule 1 is a new osteoblastic cell adhesion molecule and a diagnostic marker for osteosarcoma. , 2013, Life sciences.
[45] F. Alkuraya,et al. Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation , 2012, Journal of Medical Genetics.
[46] N. Tolwinski,et al. The many roles of PTK7: a versatile regulator of cell-cell communication. , 2012, Archives of biochemistry and biophysics.
[47] David Y. Thomas,et al. An Interaction Map of Endoplasmic Reticulum Chaperones and Foldases* , 2012, Molecular & Cellular Proteomics.
[48] V. Abraira,et al. Control of Neuronal Morphology by the Atypical Cadherin Fat3 , 2011, Neuron.
[49] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[50] Raphael Kopan,et al. The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism , 2009, Cell.
[51] M. Michalak,et al. Calreticulin, a multi-process calcium-buffering chaperone of the endoplasmic reticulum. , 2009, The Biochemical journal.
[52] W. Nelson,et al. Adherens and tight junctions: structure, function and connections to the actin cytoskeleton. , 2008, Biochimica et biophysica acta.
[53] Monica M Lurtz,et al. Intracellular calcium regulation of connexin43. , 2007, American journal of physiology. Cell physiology.
[54] T. Ogura,et al. TRIC channels are essential for Ca2+ handling in intracellular stores , 2007, Nature.
[55] F. Glorieux,et al. CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta , 2006, Cell.
[56] T. Steinberg,et al. ZO-1 alters the plasma membrane localization and function of Cx43 in osteoblastic cells , 2005, Journal of Cell Science.
[57] Q. Shi,et al. Involvement of ICAM-1 in bone metabolism: a potential target in the treatment of bone diseases? , 2005, Expert opinion on biological therapy.
[58] Jie Xu,et al. Expression of connective tissue growth factor in bone: Its role in osteoblast proliferation and differentiation in vitro and bone formation in vivo , 2003, Journal of cellular physiology.
[59] B. Yoon,et al. Connective tissue growth factor coordinates chondrogenesis and angiogenesis during skeletal development , 2003, Development.
[60] P. Marie. Role of N‐cadherin in bone formation , 2002, Journal of cellular physiology.
[61] P. Raymond,et al. Differential expression of cadherin-2 and cadherin-4 in the developing and adult zebrafish visual system , 2001, Visual Neuroscience.
[62] L. Liaw,et al. Members of the Jagged/Notch gene families are expressed in injured arteries and regulate cell phenotype via alterations in cell matrix and cell-cell interaction. , 2001, The American journal of pathology.
[63] C. Turner. Paxillin and focal adhesion signalling , 2000, Nature Cell Biology.
[64] T. Steinberg,et al. Connexin43 Deficiency Causes Delayed Ossification, Craniofacial Abnormalities, and Osteoblast Dysfunction , 2000, The Journal of cell biology.
[65] M. Itoh,et al. Involvement of ZO-1 in Cadherin-based Cell Adhesion through Its Direct Binding to α Catenin and Actin Filaments , 1997, The Journal of cell biology.
[66] B. Gumbiner,et al. Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis , 1996, Cell.
[67] H. Lee,et al. Characterization of the human full-length PTK7 cDNA encoding a receptor protein tyrosine kinase-like molecule closely related to chick KLG. , 1996, Journal of biochemistry.
[68] M T Davisson,et al. Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[69] M. Takeichi,et al. Cadherin cell adhesion receptors as a morphogenetic regulator. , 1991, Science.
[70] J. Siliciano,et al. Localization of the tight junction protein, ZO-1, is modulated by extracellular calcium and cell-cell contact in Madin-Darby canine kidney epithelial cells , 1988, The Journal of cell biology.
[71] M. Takeichi,et al. The cadherins: cell-cell adhesion molecules controlling animal morphogenesis. , 1988, Development.
[72] P. Robey,et al. Human bone cellsin vitro , 1985, Calcified Tissue International.
[73] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..
[74] P. Marie,et al. Cadherin-Mediated Cell–Cell Adhesion and Signaling in the Skeleton , 2013, Calcified Tissue International.