Results 301 to 310 of about 95,243 (337)
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The British Journal of Radiology, 1972
Abstract The appearances of a cystine kidney stone undergoing dissolution therapy suggested the presence of calcium salts. Contaminants in cystine urinary stones have been investigated by X-ray crystallography. Of 29 stones, four contained sufficient insoluble material to present problems in therapy.
D G, Shaw, D J, Sutor
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Abstract The appearances of a cystine kidney stone undergoing dissolution therapy suggested the presence of calcium salts. Contaminants in cystine urinary stones have been investigated by X-ray crystallography. Of 29 stones, four contained sufficient insoluble material to present problems in therapy.
D G, Shaw, D J, Sutor
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Current Opinion in Structural Biology, 1995
Recent reports of the crystal structure of the glycoprotein hormone human chorionic gonadotrophin show that cystine knots are proving to be versatile structural motifs that enable the construction of a variety of proteins with different functional properties.
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Recent reports of the crystal structure of the glycoprotein hormone human chorionic gonadotrophin show that cystine knots are proving to be versatile structural motifs that enable the construction of a variety of proteins with different functional properties.
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International Journal of Peptide and Protein Research, 1987
NHCH3 (X = Gly 1, Ala 2, Aib 3, Leu 4 and D‐Ala 5), have been investigated by Raman and circular dichroism (CD) spectroscopy. Solid state Raman spectra are consistent with β‐turn conformations in all five peptides. These peptides exhibit similar conformations of the disulfide segment in the solid state with a characteristic disulfide stretching ...
R. KISHORE +4 more
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NHCH3 (X = Gly 1, Ala 2, Aib 3, Leu 4 and D‐Ala 5), have been investigated by Raman and circular dichroism (CD) spectroscopy. Solid state Raman spectra are consistent with β‐turn conformations in all five peptides. These peptides exhibit similar conformations of the disulfide segment in the solid state with a characteristic disulfide stretching ...
R. KISHORE +4 more
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2018
Cystinuria, an autosomal recessive disease (estimated at 1:7000 births worldwide), results from the defective reabsorption of cystine and dibasic amino acids (also ornithine, arginine, lysine, COAL) by epithelial cells of renal proximal tubules, leading to an abnormally high urinary excretion of these amino acids.
Michel Daudon, Paul Jungers
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Cystinuria, an autosomal recessive disease (estimated at 1:7000 births worldwide), results from the defective reabsorption of cystine and dibasic amino acids (also ornithine, arginine, lysine, COAL) by epithelial cells of renal proximal tubules, leading to an abnormally high urinary excretion of these amino acids.
Michel Daudon, Paul Jungers
openaire +1 more source