缩写名/全名 |
HEMOGLOBIN
HEMOGLOBIN |
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ISSN号 | 0363-0269 | ||||||||||||||||||||||||||||
研究方向 | 医学-生化与分子生物学 | ||||||||||||||||||||||||||||
影响因子 | 2015:0.747, 2016:0.77, 2017:0.462, 2018:0.598, 2019:0.526, | ||||||||||||||||||||||||||||
出版国家 | UNITED STATES | ||||||||||||||||||||||||||||
出版周期 | Quarterly | ||||||||||||||||||||||||||||
年文章数 | 34 | ||||||||||||||||||||||||||||
出版年份 | 1976 | ||||||||||||||||||||||||||||
是否OA | No | ||||||||||||||||||||||||||||
审稿周期(仅供参考) | 较慢,6-12周 |
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录用比例 | 容易 | ||||||||||||||||||||||||||||
投稿链接 | |||||||||||||||||||||||||||||
投稿官网 | http://pdb101.rcsb.org/motm/41 | ||||||||||||||||||||||||||||
h-index | 34 | ||||||||||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0363-0269%5BISSN%5D | ||||||||||||||||||||||||||||
中科院SCI期刊分区 ( 2018年新版本) |
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中科院SCI期刊分区 ( 2020年新版本) |
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中国学者近期发表的论文 | |
1. | Hb Sichuan [α67(E16)Thr→Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin Electrophoresis. Author: Xu AP1, Chen WD1, Li J1, Zhou Y1, Zheng RY1, Li X1, Ji L1. Journal: Hemoglobin. 2018 Sep - Nov;42(5-6):330-332. doi: 10.1080/03630269.2018.1540352. Epub 2019 Jan 7. PubMed DOI |
2. | First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family. Author: He S1, Qin Q2, Lin L1, Zuo Y1, Chen Q1, Wei H1, Zheng C1, Chen B1, Qiu X1. Journal: Hemoglobin. 2018 Jul;42(4):272-275. doi: 10.1080/03630269.2018.1531018. Epub 2019 Jan 7. PubMed DOI |
3. | Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients. Author: Chen GL1, Jiang F1, Li J1, Zhou JY1, Li DZ1. Journal: Hemoglobin. 2018 Sep - Nov;42(5-6):306-309. doi: 10.1080/03630269.2018.1561461. Epub 2019 Jan 7. PubMed DOI |
4. | Detection of Hb A2 and Hb Constant Spring (HBA2: c.427T>C) by Capillary Electrophoresis in a Patient with Hb H-Hb CS Disease. Author: Li YQ1, Wei JH1, Liang L1. Journal: Hemoglobin. 2018 Sep - Nov;42(5-6):342-343. doi: 10.1080/03630269.2018.1551232. Epub 2019 Jan 9. PubMed DOI |
5. | First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene. Author: He XH1, Zhang R1, Mai GX1, Ren LR2, Li DZ3. Journal: Hemoglobin. 2018 Sep - Nov;42(5-6):344-346. doi: 10.1080/03630269.2018.1556684. Epub 2019 Jan 24. PubMed DOI |
6. | Hb H Disease Results from Compound Heterozygosity of - -SEA and -αMAL3.5 in a Chinese Family. Author: Zhao Y1, Lou J1, Sun M1, Fu Y1, Ye W1, Li Y1, Dai Y1, Liu Y1. Journal: Hemoglobin. 2019 Feb 27:1-4. doi: 10.1080/03630269.2019.1575849. [Epub ahead of print] PubMed DOI |
7. | Iron Metabolism and Oxidative Status in Patients with Hb H Disease. Author: Yao X1, Xu LH1, Xu HG1, Li XY1, Liu Y1, Fang JP1. Journal: Hemoglobin. 2019 Mar 27:1-4. doi: 10.1080/03630269.2019.1575850. [Epub ahead of print] PubMed DOI |
8. | Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene. Author: Su Q1,2, Chen S3, Wu L1, Tian R1, Yang X3, Huang X3, Chen Y1, Peng Z3, Chen J4,5. Journal: Hemoglobin. 2019 May 14:1-5. doi: 10.1080/03630269.2019.1582430. [Epub ahead of print] PubMed DOI |
9. | Unstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice. Author: Jiang H1, Zhou JY2, Li J2, Li DZ2. Journal: Hemoglobin. 2019 May 15:1-3. doi: 10.1080/03630269.2019.1582429. [Epub ahead of print] PubMed DOI |
10. | Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency? Author: Jiang F1, Li J1, Zhou JY1, Liao C1, Li DZ1. Journal: Hemoglobin. 2019 May 20:1-3. doi: 10.1080/03630269.2019.1588130. [Epub ahead of print] PubMed DOI |
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