(Q37359244)

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Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia

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Europe PubMed Central

PMC publication ID

19 August 2017

Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia (English)

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Europe PubMed Central

PMC publication ID

19 August 2017

vector-borne disease

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Mamoru Hasegawa

5

object named as

Mamoru Hasegawa

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Europe PubMed Central

PMC publication ID

19 August 2017

author name string

I-Ping Chen

1

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Europe PubMed Central

PMC publication ID

19 August 2017

Keiichi Fukuda

2

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Europe PubMed Central

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19 August 2017

Noemi Fusaki

3

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Europe PubMed Central

PMC publication ID

19 August 2017

Akihiro Iida

4

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Europe PubMed Central

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19 August 2017

Alexander Lichtler

6

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Europe PubMed Central

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19 August 2017

Ernst J Reichenberger

7

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19 August 2017

publication date

12 November 2013

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19 August 2017

Cellular Reprogramming

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19 August 2017

15

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Europe PubMed Central

PMC publication ID

19 August 2017

6

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Europe PubMed Central

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19 August 2017

503-513

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Europe PubMed Central

PMC publication ID

19 August 2017

Induced pluripotent stem cell-derived neural cells survive and mature in the nonhuman primate brain

1 reference

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Inhibition of neuronal nitric oxide synthase activity promotes migration of human-induced pluripotent stem cell-derived neural stem cells toward cancer cells

1 reference

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Transgene-free iPSCs generated from small volume peripheral blood nonmobilized CD34+ cells.

1 reference

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Reprogrammed cells for disease modeling and regenerative medicine

1 reference

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6 September 2017

Derivation of human induced pluripotent stem cells from patients with maturity onset diabetes of the young

1 reference

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A TALEN genome-editing system for generating human stem cell-based disease models

1 reference

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Transgene-free disease-specific induced pluripotent stem cells from patients with type 1 and type 2 diabetes

1 reference

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Generation of human induced pluripotent stem cells from urine samples.

1 reference

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Proteomic validation of multifunctional molecules in mesenchymal stem cells derived from human bone marrow, umbilical cord blood and peripheral blood

1 reference

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Decreased fibrocyte number is associated with atherosclerotic plaque instability in man.

1 reference

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Derivation of mesenchymal stem cells from human induced pluripotent stem cells cultured on synthetic substrates.

1 reference

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1 reference

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Efficient generation of transgene-free human induced pluripotent stem cells (iPSCs) by temperature-sensitive Sendai virus vectors

1 reference

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Hematopoietic differentiation and production of mature myeloid cells from human pluripotent stem cells

1 reference

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Methods for making induced pluripotent stem cells: reprogramming à la carte

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

6 September 2017

A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

6 September 2017

Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA.

1 reference

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6 September 2017

Reprogramming of human peripheral blood cells to induced pluripotent stem cells

1 reference

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Directed differentiation of hematopoietic precursors and functional osteoclasts from human ES and iPS cells

1 reference

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Excision of reprogramming transgenes improves the differentiation potential of iPS cells generated with a single excisable vector

1 reference

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1 reference

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Human-induced pluripotent stem cells from blood cells of healthy donors and patients with acquired blood disorders

1 reference

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iPS cells reprogrammed from human mesenchymal-like stem/progenitor cells of dental tissue origin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Generation of pluripotent stem cells from patients with type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Stoichiometric and temporal requirements of Oct4, Sox2, Klf4, and c-Myc expression for efficient human iPSC induction and differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Generation of induced pluripotent stem cells using recombinant proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

6 September 2017

Human induced pluripotent stem cells free of vector and transgene sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

6 September 2017

piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells

1 reference

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Guidelines and techniques for the generation of induced pluripotent stem cells

1 reference

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Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes

1 reference

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Induced pluripotent stem cells generated without viral integration

1 reference

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6 September 2017

Disease-specific induced pluripotent stem cells

1 reference

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Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons

1 reference

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Generation of human induced pluripotent stem cells from dermal fibroblasts

1 reference

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Reprogramming of human somatic cells to pluripotency with defined factors

1 reference

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1 reference

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Induced pluripotent stem cell lines derived from human somatic cells

1 reference

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1 reference

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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1 reference

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Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Role of the mouse ank gene in control of tissue calcification and arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Human blood dendritic cells selectively express CD83, a member of the immunoglobulin superfamily.

1 reference

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Development and function of dendritic cells in health and disease

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Recombinant Sendai viruses expressing different levels of a foreign reporter gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Craniometaphyseal and craniodiaphyseal dysplasia, head and neck manifestations and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

28 September 2017

Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Craniometaphyseal dysplasia -variability of expression within a large family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Generation of induced pluripotent stem cells from human cord blood using OCT4 and SOX2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. I. Familial metaphyseal dysplasia and craniometaphyseal dysplasia; their relation to leontiasis ossea and osteopetrosis; disorders of bone remodeling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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Optic Atrophy and Visual Loss in Craniometaphyseal Dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848480

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1 reference

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Characterization of mononucleated human peripheral blood cells.

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1 reference

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1 reference

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1 reference

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Unsuccessful consequence of optic canal decompression for a case of craniometaphyseal dysplasia.

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Craniometaphyseal dysplasia: The first successful surgical treatment for associated hearing loss

1 reference

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1 reference

https://pubmed.ncbi.nlm.nih.gov/24219578

12 December 2020

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10.1089/CELL.2013.0037

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

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Europe PubMed Central

PMC publication ID

19 August 2017

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