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Somatic Cell and Molecular Genetics|January 1, 1985
Identification of two complementation groups in Fanconi anemiaG Duckworth-Rysiecki, K Cornish, C A Clarke, et al.Developmental Medicine and Child Neurology|October 1, 1987
Magnetic resonance imaging of the brain of children with multiple sclerosisG Haas, G Schroth, I Krägeloh-Mann, et al.Deutsche Medizinische Wochenschrift (1946)|September 8, 1978
[Results of intensive care and intensive therapy of very low birth-weight infants (author's transl)]R Michaelis, M Stötter, M Buchwald, et al.Blood|December 15, 1996
Suppression of apoptosis in hematopoietic factor-dependent progenitor cell lines by expression of the FAC geneR C Cumming, J M Liu, H Youssoufian, et al.The EMBO Journal|December 8, 1998
Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasomeM A Loo, T J Jensen, L Cui, et al.The Journal of Biological Chemistry|July 25, 1992
The cystic fibrosis transmembrane regulator is present and functional in endosomes. Role as a determinant of endosomal pHG L Lukacs, X B Chang, N Kartner, et al.The Journal of Biological Chemistry|October 15, 1993
The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cellsG L Lukacs, X B Chang, C Bear, et al.The Journal of Biological Chemistry|November 1, 1996
Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activityF S Seibert, P Linsdell, T W Loo, et al.Cell|October 6, 1995
Multiple proteolytic systems, including the proteasome, contribute to CFTR processingT J Jensen, M A Loo, S Pind, et al.European Journal of Biochemistry|May 15, 1992
Quantitative expression patterns of multidrug-resistance P-glycoprotein (MDR1) and differentially spliced cystic-fibrosis transmembrane-conductance regulator mRNA transcripts in human epitheliaS Bremer, T Hoof, M Wilke, et al.Pageof 24