Literature DB >> 27701781

Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion.

Abdelhafid Natiq1,2, Philippe A Lysy3, Nynke Gillemans4, Rianne Schaap5, Abdelaziz Sefiani1,6, Saaid Amzazi2, Siham Chafai El-Alaoui1,6, Ileana Cantú4, Bella Banjanin4, Kirsten van Lom7, Cornelis L Harteveld5, Sjaak Philipsen4.   

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Year:  2016        PMID： 27701781     DOI： 10.1002/ajh.24574

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  2 in total

1.  Single-nucleotide-level mapping of DNA regulatory elements that control fetal hemoglobin expression.

Authors:  Li Cheng; Yichao Li; Qian Qi; Peng Xu; Ruopeng Feng; Lance Palmer; Jingjing Chen; Ruiqiong Wu; Tiffany Yee; Jingjing Zhang; Yu Yao; Akshay Sharma; Ross C Hardison; Mitchell J Weiss; Yong Cheng
Journal:  Nat Genet       Date:  2021-05-06       Impact factor: 38.330

2.  Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.

Authors:  Joseph Borg; Emile van den Akker; Sjaak Philipsen; Steven Heshusius; Laura Grech; Nynke Gillemans; Rutger W W Brouwer; Xander T den Dekker; Wilfred F J van IJcken; Benjamin Nota; Alex E Felice; Thamar B van Dijk; Marieke von Lindern
Journal:  Sci Rep       Date:  2022-01-10       Impact factor: 4.379
  2 in total

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