Similar articles for PMID: 25921504

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1965	1
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2022	6
2023	3
2024	1

1

Molecular identification of rare FY*Null and FY*X alleles in Caucasian thalassemic family from Sardinia.

Manfroi S, Scarcello A, Pagliaro P. Manfroi S, et al. Transfus Apher Sci. 2015 Oct;53(2):225-7. doi: 10.1016/j.transci.2015.04.013. Epub 2015 Apr 15. Transfus Apher Sci. 2015. PMID: 25921504

2

Duffy blood group phenotype-genotype correlations using high-resolution melting analysis PCR and microarray reveal complex cases including a new null FY*A allele: the role for sequencing in genotyping algorithms.

Lopez GH, Morrison J, Condon JA, Wilson B, Martin JR, Liew YW, Flower RL, Hyland CA. Lopez GH, et al. Vox Sang. 2015 Oct;109(3):296-303. doi: 10.1111/vox.12273. Epub 2015 Apr 20. Vox Sang. 2015. PMID: 25900316

3

FY*X real-time polymerase chain reaction with melting curve analysis associated with a complete one-step real-time FY genotyping.

Ansart-Pirenne H, Martin-Blanc S, Le Pennec PY, Rouger P, Cartron JP, Tournamille C. Ansart-Pirenne H, et al. Vox Sang. 2007 Feb;92(2):142-7. doi: 10.1111/j.1423-0410.2006.00872.x. Vox Sang. 2007. PMID: 17298577

4

Molecular characterization of the Fy(a-b-) phenotype in a Polish family.

Karolak E, Grodecka M, Suchanowska A, Klausa E, Bochenek S, Majorczyk E, Czerwiński M, Waśniowska K. Karolak E, et al. Transfus Apher Sci. 2013 Oct;49(2):313-7. doi: 10.1016/j.transci.2013.06.006. Epub 2013 Jun 29. Transfus Apher Sci. 2013. PMID: 23820435 Clinical Trial.

5

A novel FY allele in Brazilians.

Castilho L, Rios M, Pellegrino J Jr, Saad ST, Costa FF, Reid ME. Castilho L, et al. Vox Sang. 2004 Oct;87(3):190-5. doi: 10.1111/j.1423-0410.2004.00554.x. Vox Sang. 2004. PMID: 15569072

6

Duffy Blood Group System.

Maheshwari A, Killeen RB. Maheshwari A, et al. 2023 May 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 May 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 35593798 Free Books & Documents.

7

Molecular mechanisms that lead to reduced expression of duffy antigens.

Yazdanbakhsh K, Rios M, Storry JR, Kosower N, Parasol N, Chaudhuri A, Reid ME. Yazdanbakhsh K, et al. Transfusion. 2000 Mar;40(3):310-20. doi: 10.1046/j.1537-2995.2000.40030310.x. Transfusion. 2000. PMID: 10738032

8

A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype.

Parasol N, Reid M, Rios M, Castilho L, Harari I, Kosower NS. Parasol N, et al. Blood. 1998 Oct 1;92(7):2237-43. Blood. 1998. PMID: 9746760 Free article.

9

DARC alleles and Duffy phenotypes in African Americans.

Schmid P, Ravenell KR, Sheldon SL, Flegel WA. Schmid P, et al. Transfusion. 2012 Jun;52(6):1260-7. doi: 10.1111/j.1537-2995.2011.03431.x. Epub 2011 Nov 14. Transfusion. 2012. PMID: 22082243 Free PMC article.

10

The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein.

Olsson ML, Smythe JS, Hansson C, Poole J, Mallinson G, Jones J, Avent ND, Daniels G. Olsson ML, et al. Br J Haematol. 1998 Dec;103(4):1184-91. doi: 10.1046/j.1365-2141.1998.01083.x. Br J Haematol. 1998. PMID: 9886340 Free article.

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