Zobrazeno 1 - 10
of 38
pro vyhledávání: '"gene SLC2A10"'
Autor:
CHIARELLI, NICOLA, RITELLI, MARCO, ZOPPI, NICOLETTA, BENINI, ANNA, BORSANI, GIUSEPPE, BARLATI, SERGIO, COLOMBI, MARINA
Publikováno v:
International Journal of Developmental Biology; 2011, Vol. 55 Issue 2, p229-236, 8p
Autor:
Sergio Barlati, Anna Benini, Marina Colombi, Nicola Chiarelli, Marco Ritelli, Giuseppe Borsani, Nicoletta Zoppi
The SLC2A10 gene located on chromosome 20q13.1 encodes the facilitative glucose transporter 10 (GLUT10), a class III member of the SLC2A facilitative glucose transporter family. Mutations in the human SLC2A10 gene cause arterial tortuosity syndrome (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8aec6002c91e2ebf27484b0a38e13b2
http://hdl.handle.net/11379/55244
http://hdl.handle.net/11379/55244
Publikováno v:
Università degli Studi di Brescia-IRIS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2baafe5fd0bd4c938fb4db72fd4858e4
https://iris.unibs.it/handle/11379/528633
https://iris.unibs.it/handle/11379/528633
Autor:
Nicoletta Zoppi, Marina Colombi, Marco Ritelli, Fulvio Zaccagna, Nicola Chiarelli, L. Molisso, Marco Castori, Paola Grammatico
Publikováno v:
American Journal of Medical Genetics Part A. :1164-1169
Arterial tortuosity syndrome (ATS) is an autosomal recessive connective tissue disorder, mainly characterized by tortuosity and elongation of the large- and medium-sized arteries with predisposition to stenoses and aneurysms. ATS is caused by mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489c3607cccb5c82924a85a92ececb5a
https://doi.org/10.1002/ajmg.a.35266
https://doi.org/10.1002/ajmg.a.35266
Autor:
Inserra, Maria Cristina1 (AUTHOR) c.inserra@yahoo.it, Di Mari, Alessia2 (AUTHOR), Passaniti, Giulia3 (AUTHOR), Cannizzaro, Maria Teresa1 (AUTHOR), La Rosa, Giuliana2 (AUTHOR), Poli, Daniela4 (AUTHOR), Gitto, Placido4 (AUTHOR), Patanè, Laura3 (AUTHOR), Romeo, Placido5 (AUTHOR)
Publikováno v:
Global Medical Genetics. Dec2023, Vol. 10 Issue 4, p271-277. 7p.
Autor:
Faiyaz-Ul-Haque, Muhammad a, b, c, ⁎, Zaidi, Syed H.E. d, Al-Sanna, Nouriyah e, Alswaid, Abdulrahman f, Momenah, Tariq f, Kaya, Namik g, Al-Dayel, Fouad b, Bouhoaigah, Issam e, Saliem, Mohammed e, Tsui, Lap-Chee a, h, Teebi, Ahmad S. a, i, j
Publikováno v:
In Atherosclerosis 2009 203(2):466-471
Autor:
Tang, Chuang1 (AUTHOR), Ma, Jideng1,2 (AUTHOR), Kong, Fanli3 (AUTHOR), Li, Bo3 (AUTHOR), Du, Qinjiao1 (AUTHOR), Zhang, Yali1 (AUTHOR), Wang, Haoming1 (AUTHOR), Tang, Qianzi1 (AUTHOR), Hu, Silu1 (AUTHOR), Liu, Lingyan1 (AUTHOR), Li, Xuewei1 (AUTHOR) xuewei.li@sicau.edu.cn, Li, Mingzhou1 (AUTHOR) xuewei.li@sicau.edu.cn
Publikováno v:
Animals (2076-2615). Nov2022, Vol. 12 Issue 21, p2925. 18p.
Publikováno v:
Nutrients; Jul2024, Vol. 16 Issue 14, p2363, 20p
Autor:
Jiang, Chung-Lin1 (AUTHOR), Jen, Wei-Ping1 (AUTHOR), Tsao, Chang-Yu1 (AUTHOR), Chang, Li-Ching2 (AUTHOR), Chen, Chien-Hsiun2 (AUTHOR), Lee, Yi-Ching1 (AUTHOR) yiching@gate.sinica.edu.tw
Publikováno v:
PLoS Genetics. 5/26/2020, Vol. 16 Issue 5, p1-27. 27p.
Autor:
Szablewski, Leszek1 leszek.szablewski@wum.edu.pl
Publikováno v:
Journal of Biomedical Science. 8/31/2017, Vol. 24 Issue 1, p1-12. 12p.