Chaperoning osteogenesis: new protein-folding disease paradigms. (Q34672644)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183349%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

review article

1 reference

title

Chaperoning osteogenesis: new protein-folding disease paradigms (English)

1 reference

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18 January 2020

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0 references

3

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18 January 2020

author name string

Elena Makareeva

series ordinal

1

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18 January 2020

Nydea A Aviles

series ordinal

2

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18 January 2020

publication date

21 December 2010

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18 January 2020

published in

Trends in Cell Biology

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18 January 2020

volume

21

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18 January 2020

page(s)

168-176

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18 January 2020

issue

3

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SOST and DKK: Antagonists of LRP Family Signaling as Targets for Treating Bone Disease

18 January 2020

cites work

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FKBP10 and Bruck syndrome: phenotypic heterogeneity or call for reclassification?

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Protein kinetic stability.

7 July 2018

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Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta

7 July 2018

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Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding

7 July 2018

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Severe osteogenesis imperfecta in cyclophilin B-deficient mice

7 July 2018

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Location of 3-hydroxyproline residues in collagen types I, II, III, and V/XI implies a role in fibril supramolecular assembly

7 July 2018

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Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta

7 July 2018

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The unfolded protein response and its relevance to connective tissue diseases.

7 July 2018

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Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex

7 July 2018

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Targeted induction of endoplasmic reticulum stress induces cartilage pathology

7 July 2018

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PPIB mutations cause severe osteogenesis imperfecta

7 July 2018

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Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation

7 July 2018

1 reference

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Missense mutations that cause Bruck syndrome affect enzymatic activity, folding, and oligomerization of lysyl hydroxylase 2

7 July 2018

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A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta

7 July 2018

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Genetic control of bone formation

7 July 2018

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Converging concepts of protein folding in vitro and in vivo

7 July 2018

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alpha1-Antitrypsin deficiency, chronic obstructive pulmonary disease and the serpinopathies

7 July 2018

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Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex.

7 July 2018

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Cross-talk among bone cells

7 July 2018

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A paradigm of integrative physiology, the crosstalk between bone and energy metabolisms

7 July 2018

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Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protection

7 July 2018

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Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

7 July 2018

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The endoplasmic reticulum crossroads for newly synthesized polypeptide chains

7 July 2018

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Prolyl 4-hydroxylases, key enzymes in the synthesis of collagens and regulation of the response to hypoxia, and their roles as treatment targets

7 July 2018

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Prion protein misfolding and disease

7 July 2018

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Principles of protein misfolding

7 July 2018

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Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum

7 July 2018

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The intramolecular chaperone-mediated protein folding

7 July 2018

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The rough endoplasmic reticulum-resident FK506-binding protein FKBP65 is a molecular chaperone that interacts with collagens.

7 July 2018

1 reference

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Endoplasmic reticulum stress and autophagy as targets for cancer therapy

7 July 2018

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Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursors

7 July 2018

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The protein folding problem

7 July 2018

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Protein folding and misfolding: mechanism and principles.

7 July 2018

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ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta

7 July 2018

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Chaperone machines in action

7 July 2018

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The endoplasmic reticulum and the unfolded protein response

7 July 2018

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Procollagen triple helix assembly: an unconventional chaperone-assisted folding paradigm

7 July 2018

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Selective retention and degradation of molecules with a single mutant alpha1(I) chain in the Brtl IV mouse model of OI

7 July 2018

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Differential expression of both extracellular and intracellular proteins is involved in the lethal or nonlethal phenotypic variation of BrtlIV, a murine model for osteogenesis imperfecta

7 July 2018

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Stress to endoplasmic reticulum of mouse osteoblasts induces apoptosis and transcriptional activation for bone remodeling.

7 July 2018

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7 July 2018

ER stress and diseases.

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Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

7 July 2018

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Type I collagen in Hsp47-null cells is aggregated in endoplasmic reticulum and deficient in N-propeptide processing and fibrillogenesis

7 July 2018

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Specific recognition of the collagen triple helix by chaperone HSP47. II. The HSP47-binding structural motif in collagens and related proteins

7 July 2018

1 reference

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From acute ER stress to physiological roles of the Unfolded Protein Response

7 July 2018

1 reference

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Procollagen trafficking, processing and fibrillogenesis.

7 July 2018

1 reference

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Intracellular trafficking and degradation of unassociated proalpha2 chains of collagen type I.

7 July 2018

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7 July 2018

Osteogenesis imperfecta

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Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes

7 July 2018

1 reference

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HSP47 as a collagen-specific molecular chaperone: function and expression in normal mouse development

7 July 2018

1 reference

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The PERK eukaryotic initiation factor 2 alpha kinase is required for the development of the skeletal system, postnatal growth, and the function and viability of the pancreas

7 July 2018

1 reference

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Type I collagen is thermally unstable at body temperature

7 July 2018

1 reference

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Embryonic lethality of molecular chaperone hsp47 knockout mice is associated with defects in collagen biosynthesis

7 July 2018

1 reference

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alpha-lytic protease precursor: characterization of a structured folding intermediate

7 July 2018

1 reference

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Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function

7 July 2018

1 reference

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Hsp47 and cyclophilin B traverse the endoplasmic reticulum with procollagen into pre-Golgi intermediate vesicles. A role for Hsp47 and cyclophilin B in the export of procollagen from the endoplasmic reticulum

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

Principles that govern the folding of protein chains

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

Cyclosporin A slows collagen triple-helix formation in vivo: indirect evidence for a physiologic role of peptidyl-prolyl cis-trans-isomerase

7 July 2018

1 reference

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Osteogenesis imperfecta, normal collagen folding, and lack of cyclophilin B.

7 July 2018

1 reference

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Effect of the -Gly-3(S)-hydroxyprolyl-4(R)-hydroxyprolyl- tripeptide unit on the stability of collagen model peptides.

26 October 2018

1 reference

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Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.

26 October 2018

1 reference

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Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix

26 October 2018

1 reference

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Specific recognition of the collagen triple helix by chaperone HSP47: minimal structural requirement and spatial molecular orientation

26 October 2018

1 reference

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Unfolded conformations of alpha-lytic protease are more stable than its native state

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

Delayed triple helix formation of mutant collagen from patients with osteogenesis imperfecta.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

The influence of peptidyl-prolyl cis-trans isomerase on the in vitro folding of type III collagen.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

Protein folding in the cell: reshaping the folding funnel

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057343

Mutations Near Amino End of α1(I) Collagen Cause Combined Osteogenesis Imperfecta/Ehlers-Danlos Syndrome by Interference with N-propeptide Processing

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21183349

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21183349

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.TCB.2010.11.007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183349%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21183349%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference