(Q36861127)

16 August 2017

1 reference

title

The value of DNA analysis for antigens of the Kell and Kx blood group systems (English)

1 reference

nucleic acid sequence analysis

16 August 2017

main subject

1 reference

Soohee Lee

1

1 reference

16 August 2017

language of work or name

1 reference

1 July 2007

1 reference

16 August 2017

1 reference

16 August 2017

volume

47

1 reference

16 August 2017

issue

1 Suppl

1 reference

16 August 2017

page(s)

32S-9S

1 reference

Association of XK and Kell blood group proteins

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular cloning and primary structure of Kell blood group protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Active amino acids of the Kell blood group protein and model of the ectodomain based on the structure of neutral endopeptidase 24.11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular basis of Kell blood group phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular basis of the K:6,-7 [Js(a+b-)] phenotype in the Kell blood group system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Endothelin-3-converting enzyme activity of the KEL1 and KEL6 phenotypes of the Kell blood group system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Functional and structural aspects of the Kell blood group system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular defects underlying the Kell null phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Onset of expression of the components of the Kell blood group complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Prenatal typing of Rh and Kell blood group system antigens: the edge of a watershed

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

McLeod phenotype without the McLeod syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

McLeod neuroacanthocytosis: genotype and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

A spontaneous novel XK gene mutation in a patient with McLeod syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Point mutations causing the McLeod phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Point mutations in KEL exon 8 determine a high-incidence (RAZ) and a low-incidence (KEL25, VLAN) antigen of the Kell blood group system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

McLeod syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

A McLeod phenotype detected by random screening for K:-4 [Kp(b-)] blood donors in Brazil.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

Analysis of deletions in three McLeod patients: exclusion of the XS locus from the Xp21.1-Xp21.2 region

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1537-2995.2007.01308.X

10.1111/J.1537-2995.2007.01308.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference