Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I. (Q35153234)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25298037%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I (English)

1 reference

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20 February 2020

main subject

mucopolysaccharidosis I

1 reference

2

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20 February 2020

Pravin Patel

5

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20 February 2020

Marta Serafini

12

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20 February 2020

author name string

Alice Pievani

1

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20 February 2020

Laura Antolini

3

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20 February 2020

Tsutomu Shimada

4

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20 February 2020

Cristina Remoli

6

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20 February 2020

Benedetta Rambaldi

7

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20 February 2020

Maria Grazia Valsecchi

8

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20 February 2020

Mara Riminucci

9

1 reference

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20 February 2020

Andrea Biondi

10

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20 February 2020

Shunji Tomatsu

11

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20 February 2020

language of work or name

English

0 references

publication date

8 October 2014

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20 February 2020

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20 February 2020

volume

125

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20 February 2020

page(s)

1662-1671

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20 February 2020

issue

10

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Assay for Glycosaminoglycans by Tandem Mass Spectrometry and its Applications

20 February 2020

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Identification of infants at risk for developing Fabry, Pompe, or mucopolysaccharidosis-I from newborn blood spots by tandem mass spectrometry

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28 July 2018

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Assessment of bone dysplasia by micro-CT and glycosaminoglycan levels in mouse models for mucopolysaccharidosis type I, IIIA, IVA, and VII

28 July 2018

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Orthopaedic aspects of mucopolysaccharidoses

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28 July 2018

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Replacing the enzyme alpha-L-iduronidase at birth ameliorates symptoms in the brain and periphery of dogs with mucopolysaccharidosis type I.

28 July 2018

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Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer

28 July 2018

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Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model.

28 July 2018

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Glycosaminoglycan-mediated loss of cathepsin K collagenolytic activity in MPS I contributes to osteoclast and growth plate abnormalities

28 July 2018

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The clinical outcome of Hurler syndrome after stem cell transplantation.

28 July 2018

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Mobility in Hurler syndrome

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28 July 2018

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Correction of clinical manifestations of canine mucopolysaccharidosis I with neonatal retroviral vector gene therapy

28 July 2018

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Bone marrow transplantation for feline mucopolysaccharidosis I.

28 July 2018

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Neonatal gene therapy of MPS I mice by intravenous injection of a lentiviral vector

28 July 2018

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Long-term nonsense suppression therapy moderates MPS I-H disease progression.

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Expression in blood cells may contribute to biochemical and pathological improvements after neonatal intravenous gene therapy for mucopolysaccharidosis VII in dogs

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Musculoskeletal complications associated with lysosomal storage disorders: Gaucher disease and Hurler-Scheie syndrome (mucopolysaccharidosis type I).

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27 September 2018

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27 September 2018

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27 September 2018

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27 September 2018

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27 September 2018

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Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates.

27 September 2018

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Validation of keratan sulfate level in mucopolysaccharidosis type IVA by liquid chromatography-tandem mass spectrometry

27 September 2018

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

Neonatal bone marrow transplantation prevents liver disease in a murine model of erythropoietic protoporphyria

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12 December 2020

The controversial and changing role of haematopoietic cell transplantation for lysosomal storage disorders: an update

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12 December 2020

10.1182/BLOOD-2014-06-581207

Identifiers

DOI

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20 February 2020

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20 February 2020

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