about
FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralizationMcLeod phenotype without the McLeod syndromeTransfusion in the age of molecular diagnostics.Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.Molecular Bases and Genotyping for Rare Blood Types.McLeod syndrome: a neurohaematological disorder.Red cell antigens: Structure and function.Molecular Basis of KELnull Phenotype in Brazilians.Applications of DNA-based assays in blood group antigen and antibody identification.Genetic basis of blood group diversity.The human Kell blood group binds the erythroid 4.1R protein: new insights into the 4.1R-dependent red cell membrane complex.Overview of molecular methods in immunohematology.The value of DNA analysis for antigens of the Kell and Kx blood group systems.Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETIEndothelin-3-converting enzyme activity of the KEL1 and KEL6 phenotypes of the Kell blood group system.Untangling the Thorns: Advances in the Neuroacanthocytosis Syndromes.Expression profiles of mouse Kell, XK, and XPLAC mRNA.Clinical Significance of an Alloantibody against the Kell Blood Group Glycoprotein.Applications and Experience with PCR-Based Assays to Predict Blood Group Antigens.Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.Two novel KEL alleles encoding K0 phenotypes in Brazilians.Silent KEL alleles identified from Japanese individuals with the Ko phenotype.Three missense mutations found in the KEL gene lead to K(mod) or K0 red blood cell phenotypes.Three uncommon KEL alleles in one family with unusual Kell phenotypes explain a 35-year old conundrum.Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.Genetic diversity of KELnull and KELel: a nationwide Austrian survey.Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM.Serial blood donations for intrauterine transfusions of severe hemolytic disease of the newborn with the use of recombinant erythropoietin in a pregnant woman alloimmunized with anti-Ku.A novel KEL silencing allele in a Brazilian patient with anti-Ku.Transfusion Medicine and Molecular Genetic Methods.
P2860
Q28177435-0935E4A9-C615-45C1-AE89-4C99060F0D2FQ28288409-C3165B6C-C075-419E-8ED3-177767712A2FQ34006112-4C08B8C2-FB49-40D7-B421-DD252BB993EEQ34198997-3F5705EB-14CE-473E-8FAE-7FCBE3863E44Q34306085-E3647CE2-1892-457B-9B64-C7782154D996Q34660441-ACE159E5-B97E-4D15-BF48-7F131BAE4009Q35199789-B6F5ECD9-5EA1-4505-B015-D60C46A4CFC8Q35507341-0A7A7D02-4059-4213-99BB-3E6EFFC4F944Q35594672-1ABA432F-7D05-4281-B8C8-A78C53364485Q35880446-CCD96FD8-AF32-467E-99EA-D3E4C774CD67Q36469748-A7F4FFDA-B87B-4F87-B179-8F534F9D74EBQ36861105-389F9AB8-128F-4DED-A762-7DF7FCF08812Q36861127-832DF39D-7FD4-4CAA-8A54-9A0804C6C67CQ37042985-B023A3DC-2DCD-4E58-8869-9F4F4A29870CQ38316622-6A5619F1-AAB8-423A-BAE4-049C480CC58CQ38531994-30214F2A-41A0-4ABA-8DB1-720C34A2008CQ40190251-7635BAF6-7172-4CC2-A436-657CFF20509BQ42272382-4D1ED029-2813-4700-9277-82E9500BAAE8Q42530509-617DA2C5-45F1-4EDB-9511-5A5250319E28Q43893889-B6FAA521-9C70-4FFF-84DF-3D7E88A58B77Q43936473-41311800-933D-4E9D-A272-74A361591484Q44490619-537CC766-5694-416D-A74E-3E3E5C8FDC91Q44869368-C53D1B9B-854B-4CEE-8B87-FF7DD619976DQ45148756-16B35AF3-49E7-4BFC-B852-3E05E6E80715Q47805563-135AD668-E7CB-4B16-80F1-BD00C36D99E9Q50465161-8763FA18-D734-4320-B675-092DDF4CA659Q50472265-28BF5268-6FAC-4FE7-8E2E-4D78DEAC92DFQ50492432-4ED81220-50D2-45EA-A8C1-274858C20E4FQ50701303-F9384429-CFC9-4783-B7FC-42E39664B60DQ50723626-B29CE61F-02C7-473C-8789-E611C0936388Q50749961-63979CE8-63FB-4A24-97E3-A3B3EF6B96DCQ53661976-A985D486-58A2-4F59-BBAB-89F8CC40C5BDQ55234148-861DA4F5-F8E3-424A-BE50-7F81F282014A
P2860
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Molecular defects underlying the Kell null phenotype.
@en
type
label
Molecular defects underlying the Kell null phenotype.
@en
prefLabel
Molecular defects underlying the Kell null phenotype.
@en
P2093
P2860
P356
P1476
Molecular defects underlying the Kell null phenotype.
@en
P2093
Jovanovic-Srzentic S
Rodrigues MJ
P2860
P304
27281-27289
P356
10.1074/JBC.M103433200
P407
P577
2001-05-24T00:00:00Z