A Male Japanese Patient with Temple Syndrome Complicated by Type 2 Diabetes Mellitus-Reference-Cited by-同舟云学术

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A Male Japanese Patient with Temple Syndrome Complicated by Type 2 Diabetes Mellitus

Published:2024 Issue: Volume: Page:
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Iwanishi Masanori¹,Yorifuji Tohru²,Yamamoto Yukako¹,Ito-Kobayashi Jun¹,Shimatsu Akira¹,Kikugawa Shingo³,Kagami Masayo⁴

Affiliation:

1. Department of Diabetes and Endocrinology, Omi Medical Center, Japan

2. Second Department of Internal Medicine, Date Red Cross Hospital, Japan

3. DNA Chip Research Inc., Japan

4. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Japan

Publisher

Japanese Society of Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/advpub/0/advpub_2743-23/_pdf

Reference33 articles.

1. 1. Temple IK, Cockwell K, Hassold T, Pettay D, Jacobs P. Maternal uniparental disomy for chromosome 14. J Med Genet 28: 511-514, 1991.

2. 2. Ioannides Y, Lokulo-Sodipe K, Mackay DJG, Davis JH, Temple IK. Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases. J Med Genet 51: 495-501, 2014.

3. 3. da Silva C, Durandt C, Kallmeyer K, Ambele MA, Pepper MS. The Role of Pref-1 during Adipogenic Differentiation: An Overview of Suggested Mechanisms. Int J Mol Sci 21: 4104, 2020.

4. 4. Moon YS, Smas CM, Lee K, et al. Mice Lacking Paternally Expressed Pref-1/Dlk 1 Display Growth Retardation and accelerated Adiposity. Mol Cell Biol 22: 5585-5592, 2002.

5. 5. Kitazawa M, Hayashi S, Imamura M, et al. Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes. Development 147: dev185918, 2020.

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