المؤلفون: Baqai, Kanza, Bassetti, Jennifer A.^{Aff1, Aff2}, Kovanlikaya, Arzu^{Aff1, Aff2}, Seshan, Surya V.^{Aff1, Aff2}, Akchurin, Oleh^{Aff1, Aff2, IDs00467024063884_cor5}

المصدر: Pediatric Nephrology: Journal of the International Pediatric Nephrology Association. 39(11):3201-3204

المؤلفون: Abarca-Barriga, Hugo Hernán^{Aff1, Aff2, IDs12887024046411_cor1}, Laso-Salazar, María Cristina, Orihuela-Tacuri, Diego, Chirinos-Saire, Jenny, Venero-Nuñez, Anahí

المصدر: BMC Pediatrics. 24(1)

المؤلفون: Du, Taozi, Xia, Yu, Sun, Chengkai, Gong, Zhuwen, Liang, Lili, Gong, Zizhen, Wang, Ruifang, Lu, Deyun, Zhang, Kaichuang, Yang, Yi, Sun, Yuning, Sun, Manqing, Sun, Yu^{Aff1, Aff2}, Xiao, Bing^{Aff1, Aff2, IDs13023024030708_cor14}, Qiu, Wenjuan^{Aff1, IDs13023024030708_cor15}

المصدر: Orphanet Journal of Rare Diseases. 19(1)

المؤلفون: Hugo Hernán Abarca-Barriga, María Cristina Laso-Salazar, Diego Orihuela-Tacuri, Jenny Chirinos-Saire, Anahí Venero-Nuñez

المصدر: BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)

مصطلحات موضوعية: SLC2A2, Hypophosphatemia, Glycogen storage disease, Renal tubular acidosis, Exome sequencing, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2431

URL الوصول: https://doaj.org/article/20d5351d41b24c7cb1a7866292cc8dfd

المؤلفون: Taozi Du, Yu Xia, Chengkai Sun, Zhuwen Gong, Lili Liang, Zizhen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Manqing Sun, Yu Sun, Bing Xiao, Wenjuan Qiu

المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)

مصطلحات موضوعية: Fanconi-Bickel syndrome, SLC2A2, Glucose transporter protein 2, Variant, Regions of homozygosity, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/e7e3ae2e471947f6bc84b8442bc1926e

المؤلفون: Battal, Abdulhamit^{Aff1, IDs11033023083325_cor1}, Dogan, Abdulahad, Uyar, Ahmet, Demir, Abdulbaki, Keleş, Ömer Faruk, Celik, Ismail, Baloglu, Mehmet Cengiz, Aslan, Ali^{Aff7, Aff8}

المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 50(5):4193-4205

المؤلفون: Satoshi Yoshino, Emi Ishida, Kazuhiko Horiguchi, Shunichi Matsumoto, Yasuyo Nakajima, Atsushi Ozawa, Masanobu Yamada, Eijiro Yamada

المصدر: International Journal of Molecular Sciences, Vol 25, Iss 9, p 4704 (2024)

مصطلحات موضوعية: diabetes, beta cells, glucose responsiveness, MLL, SLC2A1, SLC2A2, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/25/9/4704; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/0726925ca76a4b4084b328505b3b4882

المؤلفون: Nicola Morrice, Susanne Vainio, Kirsi Mikkola, Lidy van Aalten, Jennifer R. Gallagher, Michael L.J. Ashford, Alison D. McNeilly, Rory J. McCrimmon, Alexandra Grosfeld, Patricia Serradas, Jukka Koffert, Ewan R. Pearson, Pirjo Nuutila, Calum Sutherland

المصدر: Molecular Metabolism, Vol 77, Iss , Pp 101807- (2023)

مصطلحات موضوعية: Diabetes, Metformin, Slc2a2, Glucose-uptake, [18F]FDG-PET, Internal medicine, RC31-1245

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2212877823001412; https://doaj.org/toc/2212-8778

URL الوصول: https://doaj.org/article/60ff9417f6b94a40a6a38abc3d1becfc

المؤلفون: Sarah Alsobaie, Arwa A. Alageel, Tahira Ishfaq, Imran Ali Khan, Khalid Khalaf Alharbi

المصدر: Diagnostics, Vol 13, Iss 20, p 3214 (2023)

مصطلحات موضوعية: polycystic ovary syndrome (PCOS), rs8192675 SNP, SLC2A2 gene, T2DM, Saudi women, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2075-4418/13/20/3214; https://doaj.org/toc/2075-4418

URL الوصول: https://doaj.org/article/c7dd3d9d0d294c7c930442df30d4fe0c

المؤلفون: Enogieru, Osatohanmwen J, Ung, Peter MU, Yee, Sook Wah, Schlessinger, Avner, Giacomini, Kathleen M

المصدر: Human Mutation. 40(7)

مصطلحات موضوعية: Biological Sciences, Genetics, Aetiology, 2.1 Biological and endogenous factors, Metabolic and endocrine, Animals, Binding Sites, Cell Membrane, Fanconi Syndrome, Female, Genetic Association Studies, Glucose, Glucose Transporter Type 2, Humans, Models, Molecular, Mutation, Oocytes, Xenopus, Fanconi-Bickel syndrome, glucose transport, GLUT2, glycogen storage, orphan disease, rare disease, rare variants, structural homology, type 2 diabetes, SLC2A2, Clinical Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/16x2m6rw