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1
Essential Pentosuria.
Br Med J. 1963 Jun 22;1(5346):1628-9.
2
Human L-xylulose reductase variation: family and population studies.
Ann Hum Genet. 1985 Jul;49(3):227-35. doi: 10.1111/j.1469-1809.1985.tb01696.x.
3
A Feeling for the Human Subject: Margaret Lasker and the Genetic Puzzle of Pentosuria.
J Hist Biol. 2021 Jun;54(2):247-274. doi: 10.1007/s10739-021-09642-9. Epub 2021 Jul 9.
4
Studies of pentose metabolism in normal subjects and in patients with pentosuria and pentosuria trait.
J Clin Endocrinol Metab. 1961 Aug;21:887-94. doi: 10.1210/jcem-21-8-887.
5
On the nature of L-xylulose reductase deficiency in essential pentosuria.
Biochem Genet. 1985 Feb;23(1-2):61-72. doi: 10.1007/BF00499113.
6
SEVEN CASES OF ESSENTIAL PENTOSURIA.
Br Med J. 1920 Nov 20;2(3125):777-9. doi: 10.1136/bmj.2.3125.777.
10
ESSENTIAL PENTOSURIA.
Va Med Mon (1918). 1965 Aug;92:385.

本文引用的文献

1
L-xylulosuria in a Lebanese family.
Am J Hum Genet. 1962 Sep;14(3):256-60.
2
Incidence of pentosuria.
N Engl J Med. 1961 Dec 7;265:1154. doi: 10.1056/NEJM196112072652308.
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Essential pentosuria: renal or enzymic disorder.
Nature. 1959 Aug 8;184 (Suppl7):463-4. doi: 10.1038/184463a0.
5
The conversion of 1-13C-D-glucuronolactone to 5-13C-L-xylulose in a pentosuric human.
Biochim Biophys Acta. 1957 Jul;25(1):196-8. doi: 10.1016/0006-3002(57)90443-2.

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