Pseudohypoparathyroidism type 1B associated with assisted reproductive technology-Reference-Cited by-同舟云学术

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology

Published:2017-01-01 Issue:10 Volume:30 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Fernandez Monica,Zambrano Maria Jose,Riquelme Joel,Castiglioni Claudia,Kottler Marie-Laure,Jüppner Harald,Mericq Veronica

Abstract

AbstractEvidence suggests an increased incidence of imprinting disorders in children conceived by assisted reproductive technologies (ART). Maternal loss-of-methylation atEstablished factsNovel Insights

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/jpem-2017-0226/pdf

Reference52 articles.

1. Imprinting disorders and assisted reproductive technology;Semin Reprod Med,2009

2. Imprinting on chromosome 20: tissue-specific imprinting and imprinting mutations in the GNAS locus;Am J Med Genet C Semin Med Genet,2010

3. Stimulation of creatine kinase BB activity by parathyroid hormone and by prostaglandin E2 in cultured bone cells;Biochem J,1985

4. A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously;Hum Reprod Update,2014

5. The autism-related gene SNRPN regulates cortical and spine development via controlling nuclear receptor Nr4a1;Sci Rep,2016

Cited by 10 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. Calcium-phosphorus metabolism and assisted reproductive technologies: intersection points;Russian Journal of Human Reproduction;2024

2. (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B;European Journal of Endocrinology;2023-12-01

3. Pseudohypoparathyroidism: complex disease variants with unfortunate names;Journal of Molecular Endocrinology;2023-11-15

4. Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib;The Journal of Clinical Endocrinology & Metabolism;2021-11-15

5. ¿Se puede diagnosticar una enfermedad genética en base a caracteres fenotípicos? A propósito de un caso de pseudohipoparatiroidismo en Ecuador;Revista de Osteoporosis y Metabolismo Mineral;2020-12