104 related articles for article (PubMed ID: 38739025)
1. Impact of transcription factors KLF1 and GATA1 on red blood cell antigen expression: a review.
Lopez GH; Sarri ME; Flower RL; Hyland CA
Immunohematology; 2024 Apr; 40(1):1-9. PubMed ID: 38739025
[TBL] [Abstract][Full Text] [Related]
2. Genetic Variants Within the Erythroid Transcription Factor, KLF1, and Reduction of the Expression of Lutheran and Other Blood Group Antigens: Review of the In(Lu) Phenotype.
Fraser NS; Knauth CM; Moussa A; Dean MM; Hyland CA; Perkins AC; Flower RL; Schoeman EM
Transfus Med Rev; 2019 Apr; 33(2):111-117. PubMed ID: 31023581
[TBL] [Abstract][Full Text] [Related]
3. Blood group phenotypes resulting from mutations in erythroid transcription factors.
Singleton BK; Frayne J; Anstee DJ
Curr Opin Hematol; 2012 Nov; 19(6):486-93. PubMed ID: 22954727
[TBL] [Abstract][Full Text] [Related]
4. Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.
Eernstman J; Veldhuisen B; Ligthart P; von Lindern M; van der Schoot CE; van den Akker E
Sci Rep; 2021 Sep; 11(1):18557. PubMed ID: 34535703
[TBL] [Abstract][Full Text] [Related]
5. Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies.
Garcia-Sanchez F; Pardi C; Kupatawintu P; Thornton N; Rodriguez MA; Lucea I; Sood C; Ochoa-Garay G
Transfusion; 2016 Jun; 56(6):1413-8. PubMed ID: 27043150
[TBL] [Abstract][Full Text] [Related]
6. Investigation of the variable In(Lu) phenotype caused by KLF1 variants.
Fraser NS; Knauth CM; Schoeman EM; Moussa A; Perkins AC; Walsh T; Millard GM; Dean MM; Hyland CA; Flower RL
Transfusion; 2018 Oct; 58(10):2414-2420. PubMed ID: 30222867
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Novel mutations in KLF1 encoding the In(Lu) phenotype reflect a diversity of clinical presentations.
Keller J; Vege S; Horn T; Keller MA; Leger RM; Aeschlimann J; Lomas-Francis C; Westhoff CM
Transfusion; 2018 Jan; 58(1):196-199. PubMed ID: 29047116
[TBL] [Abstract][Full Text] [Related]
9. Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants.
Ye L; Wang C; Li A; Li M; Pi Y; Yang J; Zhu Z; Lu D
BMC Genomics; 2024 Mar; 25(1):230. PubMed ID: 38429690
[TBL] [Abstract][Full Text] [Related]
10. Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype.
Kawai M; Obara K; Onodera T; Enomoto T; Ogasawara K; Tsuneyama H; Uchikawa M; Inaba S
Transfusion; 2017 Apr; 57(4):1072-1077. PubMed ID: 28194794
[TBL] [Abstract][Full Text] [Related]
11. Ldb1 complexes: the new master regulators of erythroid gene transcription.
Love PE; Warzecha C; Li L
Trends Genet; 2014 Jan; 30(1):1-9. PubMed ID: 24290192
[TBL] [Abstract][Full Text] [Related]
12. Lutheran.
Daniels G
Immunohematology; 2009; 25(4):152-9. PubMed ID: 20406022
[TBL] [Abstract][Full Text] [Related]
13. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype.
Singleton BK; Burton NM; Green C; Brady RL; Anstee DJ
Blood; 2008 Sep; 112(5):2081-8. PubMed ID: 18487511
[TBL] [Abstract][Full Text] [Related]
14. Identification of Lutheran Blood Groups and Genetic Variants within
Intharanut K; Khumsuk P; Nathalang O
Transfus Med Hemother; 2023 Aug; 50(4):313-320. PubMed ID: 37767278
[TBL] [Abstract][Full Text] [Related]
15. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Hariharan P; Colah R; Ghosh K; Nadkarni A
Genomics; 2019 Dec; 111(6):1771-1776. PubMed ID: 30529538
[TBL] [Abstract][Full Text] [Related]
16. Zkscan3 affects erythroblast development by regulating the transcriptional activity of GATA1 and KLF1 in mice.
Li Z; Sheng B; Zhang T; Wang T; Chen D; An G; Wang X; Meng H; Yang L
J Mol Histol; 2022 Apr; 53(2):423-436. PubMed ID: 34940950
[TBL] [Abstract][Full Text] [Related]
17. [Screening of rare blood group Lu(a-b-) phenotype and study of its molecular basis in ethnic Han Chinese from Shanghai region].
Wang C; Li Q; Guo Z; Ye L; Zhu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):238-41. PubMed ID: 24711040
[TBL] [Abstract][Full Text] [Related]
18. Novel roles for KLF1 in erythropoiesis revealed by mRNA-seq.
Tallack MR; Magor GW; Dartigues B; Sun L; Huang S; Fittock JM; Fry SV; Glazov EA; Bailey TL; Perkins AC
Genome Res; 2012 Dec; 22(12):2385-98. PubMed ID: 22835905
[TBL] [Abstract][Full Text] [Related]
19. Krüppel-like transcription factors KLF1 and KLF2 have unique and coordinate roles in regulating embryonic erythroid precursor maturation.
Vinjamur DS; Wade KJ; Mohamad SF; Haar JL; Sawyer ST; Lloyd JA
Haematologica; 2014 Oct; 99(10):1565-73. PubMed ID: 25150253
[TBL] [Abstract][Full Text] [Related]
20. A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells.
Tallack MR; Whitington T; Yuen WS; Wainwright EN; Keys JR; Gardiner BB; Nourbakhsh E; Cloonan N; Grimmond SM; Bailey TL; Perkins AC
Genome Res; 2010 Aug; 20(8):1052-63. PubMed ID: 20508144
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]