![]() ![]() ![]() What’s Shen Yue and Chen Zheyuan’s Relationship?.How is Luo Yunxi and Bai Lu’s Relationship?.Who Is Miles Wei Zheming’s Wife? Did He get Married?.Does Rosy Zhao Lusi Have a Boyfriend? Her College Boyfriend was Exposed.Does Chen Zheyuan Have A Girlfriend? What’s His Ideal Type.What is Wang Yuwen and Wang Ziqi’s Relationship?.Han Y, Zhang X (2019) Genetic diagnosis of hereditary hemochromatosis. Lescano MA, Tavares LC, Santos P (2017) Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox. Preza GC, Ruchala P, Pinon R, Ramos E, Qiao B, Peralta MA, Sharma S, Waring A, Ganz T, Nemeth E (2011) Minihepcidins are rationally designed small peptides that mimic hepcidin activity in mice and may be useful for the treatment of iron overload. īillesbolle CB, Azumaya CM, Kretsch RC, Powers AS, Gonen S, Schneider S, Arvedson T, Dror RO, Cheng Y, Manglik A (2020) Structure of hepcidin-bound ferroportin reveals iron homeostatic mechanisms. Mayr R, Janecke AR, Schranz M, Griffiths WJ, Vogel W, Pietrangelo A, Zoller H (2010) Ferroportin disease: a systematic meta-analysis of clinical and molecular findings. Īltamura S, Kessler R, Grone HJ, Gretz N, Hentze MW, Galy B, Muckenthaler MU (2014) Resistance of ferroportin to hepcidin binding causes exocrine pancreatic failure and fatal iron overload. Pietrangelo A (2010) Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment. Pietrangelo A (2017) Ferroportin disease: pathogenesis, diagnosis and treatment. Sabelli M, Montosi G, Garuti C, Caleffi A, Oliveto S, Biffo S, Pietrangelo A (2017) Human macrophage ferroportin biology and the basis for the ferroportin disease. Biochim Biophys Acta Mol Basis Dis 1864(2):464–470. Majore S, Bonaccorsi di Patti MC, Valiante M, Polticelli F, Cortese A, Di Bartolomeo S, De Bernardo C, De Muro M, Faienza F, Radio FC, Grammatico P, Musci G (2018) Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis. Qiao B, Sugianto P, Fung E, Del-Castillo-Rueda A, Moran-Jimenez MJ, Ganz T, Nemeth E (2012) Hepcidin-induced endocytosis of ferroportin is dependent on ferroportin ubiquitination. Le Tertre M, Ka C, Guellec J, Gourlaouen I, Ferec C, Callebaut I, Le Gac G (2017) Deciphering the molecular basis of ferroportin resistance to hepcidin: Structure/function analysis of rare SLC40A1 missense mutations found in suspected hemochromatosis type 4 patients. Hoffbrand AV, Taher A, Cappellini MD (2012) How I treat transfusional iron overload. Hankins JS, McCarville MB, Loeffler RB, Smeltzer MP, Onciu M, Hoffer FA, Li CS, Wang WC, Ware RE, Hillenbrand CM (2009) R2* magnetic resonance imaging of the liver in patients with iron overload. Nishina S, Tomiyama Y, Ikuta K, Tatsumi Y, Toki Y, Kato A, Kato K, Yoshioka N, Sasaki K, Hara Y, Hino K (2021) Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report. Wu LY, Song ZY, Li QH, Mou LJ, Yu YY, Shen SS, Song XX (2021) Iron chelators reverse organ damage in type 4B hereditary hemochromatosis: case reports. Zhu CY, Chen Q, Feng ZX (2021) Hereditary hemochromatosis caused by mutation in the SLC40A1 gene: a case report. Y333H mutation with gain of function of ferroportin: a recurrent cause of haemochromatosis in China. ![]() Zhang W, Xu A, Li Y, Zhao S, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Nan Y, You H, Jia J, Ou X, Huang J, China Registry of Genetic/Metabolic Liver Diseases G (2019) A novel SLC40A1 p. Zhang W, Lv T, Huang J, Ou X (2017) Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: a case report and a review of the literature. Lyu TX, Zhang W, Li XJ, Xu AJ, Zhao XY, Ou XJ, Huang J (2016) Characteristics of gene mutation in Chinese patients with hereditary hemochromatosis. Wang Y, Du Y, Liu G, Guo S, Hou B, Jiang X, Han B, Chang Y, Nie G (2017) Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis. An P, Jiang L, Guan Y, Wang H, Wang J, Tian Y, Yang W, Shi Y, Xue J, Min J, Wang F (2017) Identification of hereditary hemochromatosis pedigrees and a novel SLC40A1 mutation in Chinese population. ![]()
0 Comments
Leave a Reply. |