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KLF1 gene
Known as:
EKLF
, Kruppel-like factor 1 (erythroid)
, KRUPPEL-LIKE FACTOR 1
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This gene is involved in both transcriptional regulation and erythrocyte differentiation.
National Institutes of Health
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Related topics
Related topics
7 relations
Cell Differentiation process
Homo sapiens
KLF2 gene
Krueppel-Like Factor 1
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis.
N. Rani
,
M. Jamwal
,
+5 authors
R. Das
Blood Cells, Molecules & Diseases
2018
Corpus ID: 49715296
2017
2017
Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion
A. Natiq
,
P. Lysy
,
+9 authors
S. Philipsen
American journal of hematology/oncology
2017
Corpus ID: 12608739
FRANCESCO ZAJA,* VALENTINA TABANELLI, CLAUDIO AGOSTINELLI, ANGELICA CALLERI, ANNALISA CHIAPPELLA, MARZIA VARETTONI, PIER LUIGI…
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2017
2017
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation.
S. Satta
,
M. E. Paglietti
,
+6 authors
R. Origa
Blood Cells, Molecules & Diseases
2017
Corpus ID: 11669812
2015
2015
Changes in hematological parameters in α‐thalassemia individuals co‐inherited with erythroid Krüppel‐like factor mutations
Lihua Yu
,
Dun Liu
,
+10 authors
Xiangmin Xu
Clinical Genetics
2015
Corpus ID: 43686045
Phenotypic variations in α‐thalassemia mainly depend on the defective α‐globin gene number. Genetic modifiers of the phenotype of…
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2014
2014
Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals.
J. Lou
,
Dongzhi Li
,
+4 authors
Yanhui Liu
Blood Cells, Molecules & Diseases
2014
Corpus ID: 27396557
2013
2013
KLF1 Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin
Ting Wang
,
Yi He
,
+5 authors
Dongzhi Li
Hemoglobin
2013
Corpus ID: 32915978
We investigated the Krüppel-like factor 1 (KLF1) gene mutations in Chinese adults with increased Hb F levels (>1.5%) referred to…
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2011
2011
A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis
Y. Ravindranath
,
Gerald Goyette
,
+5 authors
Robert M. Johnson
2011
Corpus ID: 89160959
Abstract 2101[][1] Arnaud et al[a][2] recently reported on two children with an as yet unclassified CDA, characterized by…
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2007
2007
Identification of palmitate-regulated genes in HepG2 cells by applying microarray analysis.
C. Vock
,
M. Gleissner
,
Maja Klapper
,
F. Döring
Biochimica et Biophysica Acta
2007
Corpus ID: 42219845
1984
1984
Second replicon in ColV2-K94 mediates the stable coexistence of two incompatible plasmids
P. Weber
,
G. Mitra
,
S. Palchaudhuri
Journal of Bacteriology
1984
Corpus ID: 13483786
The colicin-producing plasmid pWS12, a Tn903 derivative of ColV2-K94, was found to be incompatible with the IncFI plasmids KLF1…
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1972
1972
Genetic and physicochemical characterization of Escherichia coli strains carrying fused F' elements derived from KLF1 and F57.
N. Willetts
,
F. Bastarrachea
Proceedings of the National Academy of Sciences…
1972
Corpus ID: 26660295
Although the two F' elements, F57 (carrying his(+)) and KLF1 (carrying leu(+)), cannot normally coexist in the same cell, crosses…
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