Histological characterization of retinal degeneration in mucopolysaccharidosis type IIIC-Reference-Cited by-同舟云学术

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Histological characterization of retinal degeneration in mucopolysaccharidosis type IIIC

Published:2023-04 Issue: Volume:229 Page:109433
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Ludwig Jessica,Sawant Onkar B.,Wood Jill,Singamsetty Srikanth,Pan Xuefang,Bonilha Vera L.,Rao Sujata,Pshezhetsky Alexey V.

Funder

National Eye Institute

Research to Prevent Blindness

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference21 articles.

1. A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant;Bhattacharyya;Glycobiology,2001

2. Geographic atrophy: confocal scanning laser ophthalmoscopy, histology, and inflammation in the region of expanding lesions;Bonilha;Invest. Ophthalmol. Vis. Sci.,2020

3. The genetic basis of pericentral retinitis pigmentosa-A form of mild retinitis pigmentosa;Comander;Genes,2017

4. Characterization of a C57BL/6 congenic mouse strain of mucopolysaccharidosis type IIIA;Crawley;Brain Res.,2006

5. Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B;Heldermon;PLoS One,2007

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heterologous HSPC Transplantation Rescues Neuroinflammation and Ameliorates Peripheral Manifestations in the Mouse Model of Lysosomal Transmembrane Enzyme Deficiency, MPS IIIC;Cells;2024-05-20

2. Heterologous HSPC transplantation rescues neuroinflammation and ameliorates peripheral manifestations in the mouse model of lysosomal transmembrane enzyme deficiency, MPS IIIC;2024-04-05

3. Transplantation of Wild-Type Hematopoietic Stem and Progenitor Cells Improves Disease Phenotypes in Novel Mucopolysaccharidosis Iiic Mouse Model;2024

4. Biomarkers for predicting disease course in Sanfilippo syndrome: An urgent unmet need in childhood‐onset dementia;Journal of Neurochemistry;2023-06-26

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