(Q40892818)

English

Gene transfer of the uroporphyrinogen III synthase cDNA into haematopoietic progenitor cells in view of a future gene therapy in congenital erythropoietic porphyria

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Gene transfer of the uroporphyrinogen III synthase cDNA into haematopoietic progenitor cells in view of a future gene therapy in congenital erythropoietic porphyria (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

congenital disorder

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author name string

Mazurier F

1

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Moreau-Gaudry F

2

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Salesse S

3

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Barbot C

4

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Ged C

5

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Reiffers J

6

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

de Verneuil H

7

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

publication date

1 June 1997

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Journal of Inherited Metabolic Disease

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Europe PubMed Central

PubMed publication ID

24 September 2017

20

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Europe PubMed Central

PubMed publication ID

24 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

247-257

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Europe PubMed Central

PubMed publication ID

24 September 2017

https://scigraph.springernature.com/pub.10.1023/a:1005365008147

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Cytokine stimulation of multilineage hematopoiesis from immature human cells engrafted in SCID mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of two new mutations in congenital erythropoietic porphyria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell lines.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Porphyrias: animal models and prospects for cellular and gene therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A systematic analysis of the mutations of the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Engraftment of immune-deficient mice with human hematopoietic stem cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital erythropoietic porphyria: identification and expression of 10 mutations in the uroporphyrinogen III synthase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 years.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Engraftment of immune-deficient mice with primitive hematopoietic cells from beta-thalassemia and sickle cell anemia patients: implications for evaluating human gene therapy protocols.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A spectrophotometric method for measuring hemoglobin in erythroleukemic cells (K562)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human uroporphyrinogen III synthase: molecular cloning, nucleotide sequence, and expression of a full-length cDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onset.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retroviral transduction of CD34-enriched hematopoietic progenitor cells under serum-free conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of the enzyme deficit of bone marrow cells in congenital erythropoietic porphyria by retroviral gene transfer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene transfer into hematopoietic progenitor and stem cells: progress and problems.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene therapy for adenosine deaminase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uroporphyrinogen 3 cosynthetase in human congenital erythropoietic porphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uroporphyrinogen III cosynthetase in asymptomatic carriers of congenital erythropoietic porphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of congenital erythropoietic porphyria: mutations in the human uroporphyrinogen III synthase gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CD34+ human marrow cells that express low levels of Kit protein are enriched for long-term marrow-engrafting cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presence of an autologous marrow stromal cell layer increases glucocerebrosidase gene transduction of long-term culture initiating cells (LTCICs) from the bone marrow of a patient with Gaucher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone-marrow transplantation for congenital erythropoietic porphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful cord blood stem cell transplantation for congenital erythropoietic porphyria (Gunther's disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of the enzyme defect in cultured congenital erythropoietic porphyria disease cells by retrovirus-mediated gene transfer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of congenital erythropoietic porphyria by bone marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1005365008147

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

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