Classic Galactosemia: Study on the Late Prenatal Development of GALT Specific Activity in a Sheep Model-Reference-Cited by-同舟云学术

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Classic Galactosemia: Study on the Late Prenatal Development of GALT Specific Activity in a Sheep Model

Published:2017-06-07 Issue:9 Volume:300 Page:1570-1575
ISSN:1932-8486
Container-title:The Anatomical Record
language:en
Short-container-title:Anat. Rec.

Author:

Coelho Ana I.¹²,Bierau Jörgen²,Lindhout Martijn²,Achten Jelle²,Kramer Boris W.³,Rubio-Gozalbo M. Estela¹²

Affiliation:

1. Department of Pediatrics; Maastricht University Medical Centre; Maastricht The Netherlands

2. Department of Clinical Genetics; Maastricht University Medical Centre; Maastricht The Netherlands

3. Department of Pediatrics/Neonatology; Maastricht University Medical Centre; Maastricht The Netherlands

Publisher

Wiley

Subject

Ecology, Evolution, Behavior and Systematics,Histology,Biotechnology,Anatomy

Reference44 articles.

1. The instrumented fetal sheep as a model of cerebral white matter injury in the premature infant;Back;Neurotherapeutics,2012

2. Galactose toxicity in the rat as a model for premature ovarian failure: an experimental approach readdressed;Bandyopadhyay;Hum Reprod,2003a

3. Prenatal exposure to high galactose adversely affects initial gonadal pool of germ cells in rats;Bandyopadhyay;Hum Reprod,2003b

4. Is prenatal myo-inositol deficiency a mechanism of CNS injury in galactosemia?;Berry;J Inherit Metab Dis,2011

5. Introduction to the Maastricht workshop: lessons from the past and new directions in galactosemia;Berry;J Inherit Metab Dis,2011

Cited by 7 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. Brain function in classic galactosemia, a galactosemia network (GalNet) members review;Frontiers in Genetics;2024-02-15

2. Current and Future Treatments for Classic Galactosemia;Journal of Personalized Medicine;2021-01-28

3. The Galactose Index measured in fibroblasts of GALT deficient patients distinguishes variant patients detected by newborn screening from patients with classical phenotypes;Molecular Genetics and Metabolism;2020-03

4. The 1‐ 13 C galactose breath test in GALT deficient patients distinguishes NBS detected variant patients but does not predict outcome in classical phenotypes;Journal of Inherited Metabolic Disease;2020-01-22

5. Galactose 1‐phosphate accumulates to high levels in galactose‐treated cells due to low GALT activity and absence of product inhibition of GALK;Journal of Inherited Metabolic Disease;2019-12-17

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