Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Nicole S. Fraser"'
1
Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population
Autor: Brett Wilson, Robyn M Turner, Glenda M. Millard, Yew-Wah Liew, Naomi M. Roots, Nicole S. Fraser, Robert L. Flower, Catherine A. Hyland, Genghis H. Lopez
Publikováno v: Transfusion Medicine and Hemotherapy. 47:279-287
Background: MNS blood group system genes GYPA and GYPB share a high degree of sequence homology and gene structure. Homologous exchanges between GYPA and GYPB form hybrid genes encoding hybrid glycophorins GP(A-B-A) and GP(B-A-B). Over 20 hybrid glyc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e6c255e9527c891836d5e5fdf970c477
https://doi.org/10.1159/000504026
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2
Investigation of the variable In(Lu) phenotype caused byKLF1variants
Autor: Melinda M. Dean, Assia Moussa, Nicole S. Fraser, Terry Walsh, Catherine A. Hyland, Andrew C. Perkins, Christine Knauth, Robert L. Flower, Glenda M. Millard, Elizna M. Schoeman
Publikováno v: Transfusion. 58:2414-2420
KLF1 is an essential transcriptional activator that drives erythropoiesis. KLF1 variants can result in the Inhibitor of Lutheran, or In(Lu), phenotype where red blood cells (RBCs) have reduced BCAM (LU) and CD44 (IN). Other RBC surface molecules also
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::055a0fb599cadd398e3910279bdd2797
https://doi.org/10.1111/trf.14926
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3
Frequency of Mi(a) (MNS7) and Classification of Mi(a)-Positive Hybrid Glycophorins in an Australian Blood Donor Population
Autor: Genghis H, Lopez, Brett, Wilson, Robyn M, Turner, Glenda M, Millard, Nicole S, Fraser, Naomi M, Roots, Yew-Wah, Liew, Catherine A, Hyland, Robert L, Flower
Publikováno v: Transfus Med Hemother
BACKGROUND: MNS blood group system genes GYPA and GYPB share a high degree of sequence homology and gene structure. Homologous exchanges between GYPA and GYPB form hybrid genes encoding hybrid glycophorins GP(A-B-A) and GP(B-A-B). Over 20 hybrid glyc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::eec1f958dc91679e85851ff2315a3e40
https://europepmc.org/articles/PMC7443653/
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4
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
Autor: Melinda M. Dean, Nicole S. Fraser, Catherine A. Hyland, Assia Moussa, Andrew C. Perkins, Robert L. Flower, Elizna M. Schoeman, Christine Knauth
Publikováno v: Transfusion medicine reviews. 33(2)
Erythroid-specific Kruppel-like factor 1, or KLF1, is an integral transcriptional activator for erythropoiesis. Genetic variants within KLF1 can result in a range of erythropoietic clinical phenotypes from benign to significant. The In(Lu) phenotype
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c2afff759be1cb3a4d017ceef99bc5
https://pubmed.ncbi.nlm.nih.gov/31023581
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5
Investigation of the variable In(Lu) phenotype caused by KLF1 variants
Autor: Nicole S, Fraser, Christine M, Knauth, Elizna M, Schoeman, Assia, Moussa, Andrew C, Perkins, Terry, Walsh, Glenda M, Millard, Melinda M, Dean, Catherine A, Hyland, Robert L, Flower
Publikováno v: Transfusion. 58(10)
KLF1 is an essential transcriptional activator that drives erythropoiesis. KLF1 variants can result in the Inhibitor of Lutheran, or In(Lu), phenotype where red blood cells (RBCs) have reduced BCAM (LU) and CD44 (IN). Other RBC surface molecules also
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9f70258972e6cb81d5801146842bd554
https://pubmed.ncbi.nlm.nih.gov/30222867
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