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Biochimica Et Biophysica Acta|June 30, 1985
Synthesis and secretion of the human vitamin B12-binding protein, transcobalamin II, by cultured skin fibroblasts and by bone marrow cellsM Fràter-Schröder, H J Porck, J Erten, et al.
Transplantation Proceedings|April 28, 2004
Severe rhabdomyolysis and acute renal failure in a kidney transplant patient treated with tacrolimus and chimaeric CD25 monoclonal antibodyI Fontana, F Ginevri, G Basile, et al.
Scientific Reports|March 12, 2024
Global multi-hazard risk assessment in a changing climateZélie Stalhandske, Carmen B Steinmann, Simona Meiler, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 27, 2006
Successful in vitro priming of EBV-specific CD8+ T cells endowed with strong cytotoxic function from T cells of EBV-seronegative childrenP Comoli, F Ginevri, R Maccario, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|June 28, 2000
Normal values of the bioelectrical impedance vector in childhood and pubertyT De Palo, G Messina, A Edefonti, et al.
Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.
The Journal of Clinical Investigation|September 1, 1996
Cross-linking of the dermo-epidermal junction of skin regenerating from keratinocyte autografts. Anchoring fibrils are a target for tissue transglutaminaseM Raghunath, B Höpfner, D Aeschlimann, et al.
The Journal of Biological Chemistry|April 15, 1990
In vivo and in vitro noncovalent association of excised alpha 1 (I) amino-terminal propeptides with mutant pN alpha 2(I) collagen chains in native mutant collagen in a case of Ehlers-Danlos syndrome, type VIIM K Wirtz, D R Keene, H Hori, et al.
Biochimica Et Biophysica Acta|February 26, 1999
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defectsJ T Lam, M G Martín, E Turk, et al.
Clinical Genetics|March 1, 1984
Ehlers-Danlos syndrome type IV D: an autosomal recessive disorderH M Sulh, B Steinmann, V H Rao, et al.
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