185 related articles for article (PubMed ID: 37106711)
21. Mutation screening of the Krüppel-like factor 1 gene using single-strand conformational polymorphism in a cohort of Iranian β-thalassemia patients.
Zaker-Kandjani B; Namdar-Aligoodarzi P; Azarkeivan A; Najmabadi H; Banan M
Hemoglobin; 2015; 39(1):24-9. PubMed ID: 25583416
[TBL] [Abstract][Full Text] [Related]
22. Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis.
Caria CA; Faà V; Ristaldi MS
Cells; 2022 Sep; 11(19):. PubMed ID: 36231031
[TBL] [Abstract][Full Text] [Related]
23. Hemoglobin switching in mice carrying the
Korporaal A; Gillemans N; Heshusius S; Cantú I; van den Akker E; van Dijk TB; von Lindern M; Philipsen S
Haematologica; 2021 Feb; 106(2):464-473. PubMed ID: 32467144
[TBL] [Abstract][Full Text] [Related]
24. KLF1 directly activates expression of the novel fetal globin repressor
Norton LJ; Funnell APW; Burdach J; Wienert B; Kurita R; Nakamura Y; Philipsen S; Pearson RCM; Quinlan KGR; Crossley M
Blood Adv; 2017 Apr; 1(11):685-692. PubMed ID: 29296711
[TBL] [Abstract][Full Text] [Related]
25. Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran.
Hamid M; Ershadi Oskouei S; Shariati G; Babaei E; Galehdari H; Saberi A; Sedaghat A
J Pediatr Hematol Oncol; 2018 Apr; 40(3):192-195. PubMed ID: 29420372
[TBL] [Abstract][Full Text] [Related]
26. Kruppel-like factor 1-GATA1 fusion protein improves the sickle cell disease phenotype in mice both in vitro and in vivo.
Zhu J; Li H; Aerbajinai W; Kumkhaek C; Pirooznia M; Saxena A; Dagur P; Chin K; Rodgers GP
Blood; 2022 Nov; 140(21):2276-2289. PubMed ID: 36399071
[TBL] [Abstract][Full Text] [Related]
27. Simvastatin and t-butylhydroquinone suppress KLF1 and BCL11A gene expression and additively increase fetal hemoglobin in primary human erythroid cells.
Macari ER; Schaeffer EK; West RJ; Lowrey CH
Blood; 2013 Jan; 121(5):830-9. PubMed ID: 23223429
[TBL] [Abstract][Full Text] [Related]
28. Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.
Helias V; Saison C; Peyrard T; Vera E; Prehu C; Cartron JP; Arnaud L
Hum Mutat; 2013 Jan; 34(1):221-8. PubMed ID: 23125034
[TBL] [Abstract][Full Text] [Related]
29. Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin.
Radmilovic M; Zukic B; Petrovic MS; Bartsakoulia M; Stankovic B; Kotur N; Dokmanovic L; Georgitsi M; Patrinos GP; Pavlovic S
Ann Hematol; 2013 Jan; 92(1):53-8. PubMed ID: 23161389
[TBL] [Abstract][Full Text] [Related]
30. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.
Huang J; Zhang X; Liu D; Wei X; Shang X; Xiong F; Yu L; Yin X; Xu X
Eur J Hum Genet; 2015 Oct; 23(10):1341-8. PubMed ID: 25585695
[TBL] [Abstract][Full Text] [Related]
31. Krüppel-like factor 1 (KLF1) gene single nucleotide polymorphisms in sickle cell disease and its association with disease-related morbidities.
Kumar R; Yadav R; Mishra S; Singh MPSS; Gwal A; Bharti PK; Rajasubramaniam S
Ann Hematol; 2021 Feb; 100(2):365-373. PubMed ID: 33388857
[TBL] [Abstract][Full Text] [Related]
32. miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells.
Li Y; Liu D; Zhang X; Li Z; Ye Y; Liu Q; Shen J; Chen Z; Huang H; Liang Y; Han X; Liu J; An X; Mohandas N; Xu X
Exp Hematol; 2018 Jul; 63():33-40.e2. PubMed ID: 29601850
[TBL] [Abstract][Full Text] [Related]
33. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin.
Satta S; Perseu L; Moi P; Asunis I; Cabriolu A; Maccioni L; Demartis FR; Manunza L; Cao A; Galanello R
Haematologica; 2011 May; 96(5):767-70. PubMed ID: 21273267
[TBL] [Abstract][Full Text] [Related]
34. Krüppel-Like Transcription Factor KLF1 Is Required for Optimal γ- and β-Globin Expression in Human Fetal Erythroblasts.
Vinjamur DS; Alhashem YN; Mohamad SF; Amin P; Williams DC; Lloyd JA
PLoS One; 2016; 11(2):e0146802. PubMed ID: 26840243
[TBL] [Abstract][Full Text] [Related]
35. Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
Pereira C; Relvas L; Bento C; Abade A; Ribeiro ML; Manco L
Blood Cells Mol Dis; 2015 Apr; 54(4):315-20. PubMed ID: 25842369
[TBL] [Abstract][Full Text] [Related]
36. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.
Borg J; Papadopoulos P; Georgitsi M; Gutiérrez L; Grech G; Fanis P; Phylactides M; Verkerk AJ; van der Spek PJ; Scerri CA; Cassar W; Galdies R; van Ijcken W; Ozgür Z; Gillemans N; Hou J; Bugeja M; Grosveld FG; von Lindern M; Felice AE; Patrinos GP; Philipsen S
Nat Genet; 2010 Sep; 42(9):801-5. PubMed ID: 20676099
[TBL] [Abstract][Full Text] [Related]
37. Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.
Satta S; Perseu L; Maccioni L; Giagu N; Galanello R
Blood Cells Mol Dis; 2012 Jan; 48(1):22-4. PubMed ID: 22093801
[TBL] [Abstract][Full Text] [Related]
38. Whole exome sequencing and rare variant association study to identify genetic modifiers,
Hantaweepant C; Suktitipat B; Pithukpakorn M; Chinthammitr Y; Limwongse C; Tansiri N; Sawatnatee S; Takpradit C; Rotchanapanya W; Pongudom S; Charoenprasert K; Paiboonsukwong K; Thamprasert W; Nolwachai N; Rattanasawat W; Sae-Aeng B; Khorwanichakij N; Saetow P; Saengboon S; Kamjornpreecha K; Pholmoo W; Dujjawan B; Siritanaratkul N
Hematology; 2023 Dec; 28(1):2187155. PubMed ID: 36939018
[TBL] [Abstract][Full Text] [Related]
39. Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction.
Shariati L; Modarressi MH; Tabatabaiefar MA; Kouhpayeh S; Hejazi Z; Shahbazi M; Sabzehei F; Salehi M; Khanahmad H
J Cell Biochem; 2019 May; 120(5):8438-8446. PubMed ID: 30556211
[TBL] [Abstract][Full Text] [Related]
40. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
