Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria-Reference-Cited by-同舟云学术

Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria

Published:2020-12 Issue: Volume:25 Page:100640
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Bik-Multanowski Miroslaw,Madetko-Talowska Anna,Betka Iwona,Swieczka Elzbieta,Didycz Bozena,Orchel-Szastak Karolina,Bik-Multanowska Kinga,Starostecka Ewa,Jaglowska Joanna,Mozrzymas Renata,Zolkowska Joanna,Chyz Katarzyna,Korycinska-Chaaban Dorota

Funder

National Science Centre

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference40 articles.

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3. Genetics of phenylketonuria: then and now;Blau;Hum. Mutat.,2016

4. The complete European guidelines on phenylketonuria: diagnosis and treatment;van Wegberg;Orphanet J Rare Dis.,2017

5. Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy;Acosta;J. Am. Diet. Assoc.,2003

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. LAT1-dependent placental methionine uptake is a key player in fetal programming of metabolic disease;Metabolism;2024-04

2. Management precautions for risk of obesity are necessary among infants with PKU carrying the rs113883650 variant of the LAT1 gene: A cross-sectional study;PLOS ONE;2022-02-17

3. Blood phenylalanine reduction reverses gene expression changes observed in a mouse model of phenylketonuria;Scientific Reports;2021-11-24

4. The rs113883650 variant of SLC7A5 (LAT1) gene may alter brain phenylalanine content in PKU;Molecular Genetics and Metabolism Reports;2021-06