A historical perspective on the discovery of the Kell blood group carriers von Redman, Colvin M., Lee, Soohee

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Identification of two new members, XPLAC and XTES, of the XK family von Calenda, Giulia, Peng, Jianbin, Redman, Colvin M., Sha, Quan, Wu, Xu, Lee, Soohee

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Endothelin-3-converting Enzyme Activity of the KEL1 and KEL6 Phenotypes of the Kell Blood Group System von Sha, Quan, Redman, Colvin M., Lee, Soohee

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Point mutations causing the McLeod phenotype von Russo, David C.W., Lee, Soohee, Reid, Marion E., Redman, Colvin M.

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Oxysterols suppress constitutive fibrinogen expression von Xia, Hui, Redman, Colvin M.

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Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases von Peng, Jianbin, Redman, Colvin M., Wu, Xu, Song, Xiaoling, Walker, Ruth H., Westhoff, Connie M., Lee, Soohee

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The Kell blood group system: Kell and XK membrane proteins von Lee, Soohee, Russo, David, Redman, Colvin M

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Changes in red cell ion transport, reduced intratumoral neovascularization, and some mild motor function abnormalities accompany targeted disruption of the Mouse Kell gene (Kel) von Zhu, Xiang, Rivera, Alicia, Golub, Mari S., Peng, Jianbin, Sha, Quan, Wu, Xu, Song, Xiaoling, Kumarathasan, Prem, Ho, Mac, Redman, Colvin M., Lee, Soohee

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Active amino acids of the Kell blood group protein and model of the ectodomain based on the structure of neutral endopeptidase 24.11 von Lee, Soohee, Debnath, Asim K., Redman, Colvin M.

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Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype von Lee, Soohee, Russo, David C.W., Reid, Marion E., Redman, Colvin M.

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Molecular Defects Underlying the Kell Null Phenotype von Lee, Soohee, Russo, David C.W., Reiner, Alexander P., Lee, Jeffrey H., Sy, Michael Y., Telen, Marilyn J., Judd, W. John, Simon, Philippe, Rodrigues, Maria J., Chabert, Teresa, Poole, Joyce, Jovanovic-Srzentic, Snezana, Levene, Cyril, Yahalom, Vered, Redman, Colvin M.

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Onset of expression of the components of the Kell blood group complex von Pu, Jeffrey J., Redman, Colvin M., Visser, Jan W.M., Lee, Soohee

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Fibrinogen Biosynthesis von REDMAN, COLVIN M., XIA, HUI

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A historical perspective on the discovery of the K ell blood group carriers von Redman, Colvin M., Lee, Soohee

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The McLeod syndrome: an example of the value of integrating clinical and molecular studies von Redman, Colvin M., Reid, Marion E.

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Kell, Kx and the McLeod syndrome von Redman, Colvin M, Russo, David, Lee, Soohee

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First example of anti‐Kx in a person with the McLeod phenotype and without chronic granulomatous disease von Russo, David C., Øyen, Ragnhild, Powell, Vivien I., Perry, Sherry, Hitchcock, Judith, Redman, Colvin M., Reid, Marion E.

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Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion von Redman, C M, Xia, H

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Assembly and Secretion of Fibrinogen von Zhang, Jian-Zhong, Redman, Colvin M.

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Secretion of Biologically Active Recombinant Fibrinogen by Yeast (∗) von Roy, Samar N., Kudryk, Bohdan, Redman, Colvin M.

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