(Q45882623)

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Correction of a mineralization defect by overexpression of a wild-type cDNA for COL1A1 in marrow stromal cells (MSCs) from a patient with osteogenesis imperfecta: a strategy for rescuing mutations that produce dominant-negative protein defects

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

Correction of a mineralization defect by overexpression of a wild-type cDNA for COL1A1 in marrow stromal cells (MSCs) from a patient with osteogenesis imperfecta: a strategy for rescuing mutations that produce dominant-negative protein defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

osteogenesis imperfecta

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1 reference

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Radhika Pochampally

1

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

author name string

Horwitz EM

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

DiGirolamo CM

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

Stokes DS

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

Prockop DJ

5

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

publication date

1 July 2005

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

12

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

14

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

1119-1125

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

https://scigraph.springernature.com/pub.10.1038/sj.gt.3302514

0 references

Collagens and collagen-related diseases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Marrow stromal cells as a source of progenitor cells for nonhematopoietic tissues in transgenic mice with a phenotype of osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Clinical responses to bone marrow transplantation in children with severe osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone

1 reference

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21 January 2018

Allogeneic mesenchymal stem cell infusion for treatment of metachromatic leukodystrophy (MLD) and Hurler syndrome (MPS-IH).

1 reference

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21 January 2018

Randomized cross-over trial of progenitor-cell mobilization: high-dose cyclophosphamide plus granulocyte colony-stimulating factor (G-CSF) versus granulocyte-macrophage colony-stimulating factor plus G-CSF.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Procollagen with skipping of alpha 1(I) exon 41 has lower binding affinity for alpha 1(I) C-telopeptide, impaired in vitro fibrillogenesis, and altered fibril morphology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

A gene-targeting approach identifies a function for the first intron in expression of the alpha1(I) collagen gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Collagen alpha1(I) gene contains an element responsive to tumor necrosis factor-alpha located in the 5' untranslated region of its first exon

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

One strategy for cell and gene therapy: harnessing the power of adult stem cells to repair tissues.

1 reference

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21 January 2018

High proportion of mutant osteoblasts is compatible with normal skeletal function in mosaic carriers of osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Osteogenesis imperfecta: prospects for molecular therapeutics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

RNAi of COL1A1 in mesenchymal progenitor cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Gene targeting in stem cells from individuals with osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Rapidly forming apatitic mineral in an osteoblastic cell line (UMR 106-01 BSP).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

21 January 2018

Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

7 January 2021

based on heuristic

inferred from DOI database lookup

Col1a1-GFP transgene expression in developing incisors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

7 January 2021

based on heuristic

inferred from DOI database lookup

Three novel type I collagen mutations in osteogenesis imperfecta type IV probands are associated with discrepancies between electrophoretic migration of osteoblast and fibroblast collagen

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

7 January 2021

based on heuristic

inferred from DOI database lookup

Tissue-specific expression of the gene for type I procollagen (COL1A1) in transgenic mice. Only 476 base pairs of the promoter are required if collagen genes are used as reporters

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic cell mosaicism: Another source of phenotypic heterogeneity in nuclear families with osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302514

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.GT.3302514

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

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https://api.fatcat.wiki/v0/release/sbi62y7morb4hctjmlcyjnyeci

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/15815702

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