Literature DB >> 15142125

Erythropoietin receptor defect: a cause of primary polycythaemia.

K B Petersen, P Hokland, G B Petersen, C G Nyvold, K Brorson Petersen, G Bruun Petersen, C Guldborg Nyvold.   

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Year:  2004        PMID： 15142125     DOI： 10.1111/j.1365-2141.2004.04931.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  4 in total

1.  A novel mutation of the erythropoietin receptor gene associated with primary familial and congenital polycythaemia.

Authors:  Kacey O'Rourke; David J Fairbairn; Kathryn A Jackson; Kirk L Morris; Siok-Keen Tey; Glen A Kennedy
Journal:  Int J Hematol       Date:  2011-03-25       Impact factor: 2.490

Review 2.  Advances in understanding the pathogenesis of primary familial and congenital polycythaemia.

Authors:  Lily J Huang; Yu-Min Shen; Gamze B Bulut
Journal:  Br J Haematol       Date:  2010-01-20       Impact factor: 6.998

3.  New pathogenic mechanisms induced by germline erythropoietin receptor mutations in primary erythrocytosis.

Authors:  Florence Pasquier; Caroline Marty; Thomas Balligand; Frédérique Verdier; Sarah Grosjean; Vitalina Gryshkova; Hana Raslova; Stefan N Constantinescu; Nicole Casadevall; William Vainchenker; Christine Bellanné-Chantelot; Isabelle Plo
Journal:  Haematologica       Date:  2017-12-21       Impact factor: 9.941

Review 4.  Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis.

Authors:  Danijela Vočanec; Tinkara Prijatelj; Nataša Debeljak; Tanja Kunej
Journal:  Int J Lab Hematol       Date:  2018-12-03       Impact factor: 2.877
  4 in total

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