[1]
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NUCLEOTIDE SEQUENCE [MRNA].
DOI=10.1016/0092-8674(94)90136-8; PubMed=8004674 [NCBI, ExPASy, EBI, Israel, Japan]
Ho M.,
Chelly J.,
Carter N.,
Danek A.,
Crocker P.,
Monaco A.P.;
"Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.";
Cell 77:869-880(1994).
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[2]
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SEQUENCE REVISION TO 204-205.
Ho M.;
Submitted (MAY-1999) to the EMBL/GenBank/DDBJ databases.
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[3]
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NUCLEOTIDE SEQUENCE [MRNA].
Huang C.-H.,
Chen Y.;
"A superfamily of XK-related genes (XRG) widely expressed in vertebrates and invertebrates.";
Submitted (JAN-2004) to the EMBL/GenBank/DDBJ databases.
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[4]
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NUCLEOTIDE SEQUENCE [GENOMIC DNA].
Rieder M.J.,
Johanson E.J.,
da Ponte S.H.,
Hastings N.C.,
Ahearn M.O.,
Bertucci C.B.,
Wong M.W.,
Yi Q.,
Nickerson D.A.;
"SeattleSNPs. NHLBI HL66682 program for genomic applications, UW-FHCRC, Seattle, WA (URL: http://pga.gs.washington.edu).";
Submitted (MAY-2005) to the EMBL/GenBank/DDBJ databases.
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[5]
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NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
TISSUE=Testis;
DOI=10.1101/gr.2596504; PubMed=15489334 [NCBI, ExPASy, EBI, Israel, Japan]
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
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[6]
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PROTEIN SEQUENCE OF 1-22, AND LACK OF GLYCOSYLATION.
PubMed=7737196 [NCBI, ExPASy, EBI, Israel, Japan]
Khamlichi S.,
Bailly P.,
Blanchard D.,
Goossens D.,
Cartron J.-P.,
Bertrand O.;
"Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients.";
Eur. J. Biochem. 228:931-934(1995).
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[7]
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SUBUNIT, DISULFIDE BOND, AND MUTAGENESIS OF CYS-347.
DOI=10.1074/jbc.273.22.13950; PubMed=9593744 [NCBI, ExPASy, EBI, Israel, Japan]
Russo D.,
Redman C.,
Lee S.;
"Association of XK and Kell blood group proteins.";
J. Biol. Chem. 273:13950-13956(1998).
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[8]
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PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-63, AND MASS SPECTROMETRY.
TISSUE=Epithelium;
DOI=10.1016/j.cell.2006.09.026; PubMed=17081983 [NCBI, ExPASy, EBI, Israel, Japan]
Olsen J.V.,
Blagoev B.,
Gnad F.,
Macek B.,
Kumar C.,
Mortensen P.,
Mann M.;
"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.";
Cell 127:635-648(2006).
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[9]
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VARIANT MLS ARG-294.
DOI=10.1002/ana.10035; PubMed=11761473 [NCBI, ExPASy, EBI, Israel, Japan]
Danek A.,
Rubio J.P.,
Rampoldi L.,
Ho M.,
Dobson-Stone C.,
Tison F.,
Symmans W.A.,
Oechsner M.,
Kalckreuth W.,
Watt J.M.,
Corbett A.J.,
Hamdalla H.H.,
Marshall A.G.,
Sutton I.,
Dotti M.T.,
Malandrini A.,
Walker R.H.,
Daniels G.,
Monaco A.P.;
"McLeod neuroacanthocytosis: genotype and phenotype.";
Ann. Neurol. 50:755-764(2001).
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[10]
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VARIANT MLS GLY-222.
DOI=10.1046/j.1537-2995.2002.00049.x; PubMed=11961232 [NCBI, ExPASy, EBI, Israel, Japan]
Russo D.C.,
Lee S.,
Reid M.E.,
Redman C.M.;
"Point mutations causing the McLeod phenotype.";
Transfusion 42:287-293(2002).
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[11]
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VARIANT MLS LYS-327.
DOI=10.1046/j.1537-2995.2003.t01-1-00434.x; PubMed=12823753 [NCBI, ExPASy, EBI, Israel, Japan]
Jung H.H.,
Hergersberg M.,
Vogt M.,
Pahnke J.,
Treyer V.,
Rothlisberger B.,
Kollias S.S.,
Russo D.,
Frey B.M.;
"McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.";
Transfusion 43:928-938(2003).
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