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3
Sanfilippo disease type B: enzyme replacement and metabolic correction in cultured fibroblasts.
Science. 1973 Aug 24;181(4101):753-5. doi: 10.1126/science.181.4101.753.
4
Sanfilippo A syndrome: sulfamidase deficiency in cultured skin fibroblasts and liver.
J Clin Invest. 1974 Oct;54(4):907-12. doi: 10.1172/JCI107830.
5
The sanfilippo B corrective factor: a N-acetyl-alpha-D-glucosamindiase.
Biochem Biophys Res Commun. 1972 Jul 25;48(2):262-9. doi: 10.1016/s0006-291x(72)80044-5.

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5
Pinocytosis in fibroblasts. Quantitative studies in vitro.
J Cell Biol. 1974 Dec;63(3):949-69. doi: 10.1083/jcb.63.3.949.
6
Membrane flow during pinocytosis. A stereologic analysis.
J Cell Biol. 1976 Mar;68(3):665-87. doi: 10.1083/jcb.68.3.665.
9
Endocytosis of sulphated proteoglycans by cultured skin fibroblasts.
Biochem J. 1978 Dec 15;176(3):671-6. doi: 10.1042/bj1760671.

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1
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75.
4
Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion.
Proc Natl Acad Sci U S A. 1971 Feb;68(2):303-7. doi: 10.1073/pnas.68.2.303.
5
A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes.
Biochem Biophys Res Commun. 1972 Nov 15;49(4):992-9. doi: 10.1016/0006-291x(72)90310-5.
10
The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.
Proc Natl Acad Sci U S A. 1972 Aug;69(8):2048-51. doi: 10.1073/pnas.69.8.2048.

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