Soohee Lee

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Phenotypic variation among brothers with the McLeod neuroacanthocytosis syndrome

Hans H. Jung, A. Danek, F. Tison, 2007, Movement disorders : official journal of the Movement Disorder Society.

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

A. Debnath, Soohee Lee, C. Redman, 2003, Blood.

Effect of phosphatidylserine on the shape of McLeod red cell acanthocytes

Soohee Lee, E. Robbins, W. Marsh, 1989 .

Endothelin-3-converting Enzyme Activity of the KEL1 and KEL6 Phenotypes of the Kell Blood Group System*

Soohee Lee, C. Redman, Q. Sha, 2006, Journal of Biological Chemistry.

Recent Studies of Kell and XK: Expression Profi les of Mouse Kell and XK mRNA

Soohee Lee, Q. Sha, X. Zhu, 2008 .

Expression Profiles of Mouse Kell, XK, and XPLAC mRNA

Soohee Lee, G. Calenda, Q. Sha, 2007, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

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

Soohee Lee, J. Visser, C. Redman, 2005, Transfusion.

The Kell Blood Group Protein, its Relation to XK and its Function as an Endothelin-3-Converting Enzyme

Soohee Lee, C. Redman, D. Russo, 2004 .

Molecular Defects Underlying the Kell Null Phenotype*

M. Telen, C. Levene, J. Poole, 2001, The Journal of Biological Chemistry.

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

Soohee Lee, 2007, Transfusion.

McLeod phenotype without the McLeod syndrome

A. Danek, M. Reid, I. Uttner, 2007, Transfusion.

Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases.

C. Westhoff, R. Walker, Soohee Lee, 2007, Gene.

Molecular Basis of Kell Blood Group Phenotypes

Soohee Lee, 1997, Vox sanguinis.

Detection of a Large W hite-Specific Duplication in D-loop Region of the Porcine MtDNA . Jae#Hwan

Soohee Lee, C. Cho, H.-Y. Han, 2009 .

Spontaneously arising red cells with a McLeod-like phenotype in normal donors.

Soohee Lee, K. Sanders, J. Pu, 2009, Mutation research.

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

A. Debnath, C. Lomas‐Francis, M. Reid, 2006, Transfusion.

Dexmedetomidine-induced contraction involves tyrosine kinase-mediated calcium sensitization in isolated rat aortae

Jaehwan Kim, Jiyoong Kim, R. Subbarao, 2018 .

Kell Blood-Group Protein

Soohee Lee, C. Redman, 2004 .

Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype

M. Reid, Soohee Lee, C. Redman, 2003, Transfusion.

Point mutations causing the McLeod phenotype

M. Reid, Soohee Lee, C. Redman, 2002, Transfusion.

Association of XK and Kell Blood Group Proteins*

Soohee Lee, S. Lee, C. Redman, 1998, The Journal of Biological Chemistry.

Kell Blood Group System and the McLeod Syndrome

Soohee Lee, C. Redman, 1995 .

Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis.

Soohee Lee, J. Romero, M. Ho, 2013, Blood cells, molecules & diseases.

Two McLeod patients with novel mutations in XK

C. Singer, H. Fernandez, C. Lomas‐Francis, 2011, Journal of the Neurological Sciences.

The mouse Kell blood group gene (Kel): cDNA sequence, genomic organization, expression, and enzymatic function

Soohee Lee, C. Redman, D. Russo, 2000, Immunogenetics.

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 KETI

A. Debnath, W. Flegel, T. Peyrard, 2013, Transfusion.

Changes in red cell ion transport, reduced intratumoral neovascularization, and some mild motor function abnormalities accompany targeted disruption of the Mouse Kell gene (Kel)

M. Golub, P. Kumarathasan, Soohee Lee, 2009, American journal of hematology.

A historical perspective on the discovery of the Kell blood group carriers

Soohee Lee, C. Redman, 2013, Transfusion.

Protein 4.1R-dependent multiprotein complex: New insights into the structural organization of the red blood cell membrane

Yang Yang, J. Hartwig, N. Mohandas, 2008, Proceedings of the National Academy of Sciences.

Giant axon formation in mice lacking Kell, XK, or Kell and XK: animal models of McLeod neuroacanthocytosis syndrome.

E. Cho, R. Walker, Soohee Lee, 2014, The American journal of pathology.

Identification of two new members, XPLAC and XTES, of the XK family.

Soohee Lee, C. Redman, G. Calenda, 2006, Gene.

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

Soohee Lee, S. Lee, C. Redman, 1995, Transfusion.

Molecular basis of the Kell (K1) phenotype.

M. Reid, Soohee Lee, S. Lee, 1995, Blood.

Molecular cloning and primary structure of Kell blood group protein.

Soohee Lee, W. Marsh, S. Lee, 1991, Proceedings of the National Academy of Sciences of the United States of America.

The Kell blood group system: Kell and XK membrane proteins.

Soohee Lee, S. Lee, C. Redman, 2000, Seminars in hematology.

Proteolytic processing of big endothelin-3 by the kell blood group protein.

A. Mele, Y. Cao, Soohee Lee, 1999, Blood.

Functional and structural aspects of the Kell blood group system.

Soohee Lee, S. Lee, C. Redman, 2000, Transfusion medicine reviews.

Expression of Kell blood group protein in nonerythroid tissues.

Soohee Lee, S. Lee, C. Redman, 2000, Blood.

Kell, Kx and the McLeod syndrome.

Soohee Lee, S. Lee, C. Redman, 1999, Bailliere's best practice & research. Clinical haematology.

Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles

P. Sistonen, M. Reid, Soohee Lee, 1996, Transfusion.

The human Kell blood group gene maps to chromosome 7q33 and its expression is restricted to erythroid cells.

Soohee Lee, W. Marsh, S. Lee, 1993, Blood.

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

A. Debnath, Soohee Lee, C. Redman, 2013 .