Literature DB >> 23594618

Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I.

Katarzyna Rawa1, Liliana Chelmecka-Hanusiewicz, Danuta Plochocka, Katarzyna Pawinska-Wasikowska, Walentyna Balwierz, Beata Burzynska.   

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Year:  2013        PMID： 23594618     DOI： 10.1159/000347041

Source DB:  PubMed          Journal:  Acta Haematol        ISSN： 0001-5792            Impact factor:   2.195


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  1 in total

1.  Cytochrome B5 type A alleviates HCC metastasis via regulating STOML2 related autophagy and promoting sensitivity to ruxolitinib.

Authors:  Hongrui Guo; Shuhang Liang; Yan Wang; Shuo Zhou; Dalong Yin; Shugeng Zhang; Jizhou Wang; Dehai Wu; Kun Ma; Yufeng Liu; Linmao Sun; Changyong Ji; Xianying Li; Huanran Zhou; Guangchao Yang; Xinyu Guo; Tianming Cui; Zihao Li; Yao Liu; Jiabei Wang; Lianxin Liu
Journal:  Cell Death Dis       Date:  2022-07-18       Impact factor: 9.685
  1 in total

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