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Items: 1 to 20 of 102

1.

Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase.

Christensen M, Duno M, Lund AM, Skovby F, Christensen E.

J Inherit Metab Dis. 2007 Apr;30(2):248-55. Epub 2007 Mar 1.

PMID:
17334708
2.

HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE.

KOMROWER GM, WILSON V, CLAMP JR, WESTALL RG.

Arch Dis Child. 1964 Jun;39:250-6. No abstract available.

3.

Vitamin B6 dependent xanthurenic aciduria.

Tada K, Yokoyama Y, Nakagawa H, Yoshida T, Arakawa T.

Tohoku J Exp Med. 1967 Oct;93(2):115-24. No abstract available.

4.

Familial hydroxykynureninuria.

Reddi OS, Reddy MV, Reddy KR.

Hum Hered. 1978;28(3):238-40. No abstract available.

PMID:
649181
5.

[B6-dependent xanthurenic aciduria].

Tada K, Yokoyama Y.

Tanpakushitsu Kakusan Koso. 1968 Apr;13(4):311-8. Japanese. No abstract available.

PMID:
5749458
6.

[Kynureninase deficiency].

Ohura T.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):255-7. Review. Japanese. No abstract available.

PMID:
9590041
7.

[Studies of tryptophan metabolism in cancer of the urinary bladder].

Wich H, Grimm U, Knapp A.

Z Urol Nephrol. 1989 Nov;82(11):593-6. German.

PMID:
2618183
8.

Abnormal red body coloration of the silkworm, Bombyx mori, is caused by a mutation in a novel kynureninase.

Meng Y, Katsuma S, Mita K, Shimada T.

Genes Cells. 2009 Feb;14(2):129-40. doi: 10.1111/j.1365-2443.2008.01257.x. Epub 2008 Jan 6.

9.

3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase.

Sass JO, Walter M, Shield JP, Atherton AM, Garg U, Scott D, Woods CG, Smith LD.

J Inherit Metab Dis. 2012 May;35(3):437-42. doi: 10.1007/s10545-011-9381-x. Epub 2011 Aug 24.

PMID:
21863277
10.

A common mutation among blacks with mut- methylmalonic aciduria.

Adjalla CE, Hosack AR, Matiaszuk NV, Rosenblatt DS.

Hum Mutat. 1998;Suppl 1:S248-50. No abstract available.

PMID:
9452100
11.

Alterations of the tryptophan--nicotinic acid metabolism in vitiligo.

De Antoni A, Cardin Dè Stefani EL, Costa C, Vanzan S, Allegri G.

Acta Vitaminol Enzymol. 1982;4(3):237-43.

PMID:
7148608
12.

On kynureninase activity.

Shibata Y, Takeuchi F, Tsubouchi R, Haneda M, Ohta T, Nakatsuka M, Nisimoto Y, Tamai T, Nomura S, Fujimoto H, et al.

Adv Exp Med Biol. 1991;294:523-6.

PMID:
1772086
13.

Vitamin B6 dependent xanthurenic aciduria (the second report).

Tada K, Yokoyama Y, Nakagawa H, Arakawa T.

Tohoku J Exp Med. 1968 Jun;95(2):107-14. No abstract available.

14.

[Mutation analysis of the MMACHC gene in a pedigree with methylmalonic aciduria].

Tang H, Hao H, Tang SH, Chen X, Liu F, Cha QB, Li YQ, Li HJ, Sun L, Yu M, Xiao X, Zhou TH.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):62-5. doi: 10.3760/cma.j.issn.1003-9406.2009.01.014. Chinese.

PMID:
19199254
15.

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population.

Zhang Y, Shen J, He X, Zhang K, Wu S, Xiao B, Zhou X, Phillips RS, Gao P, Jeunemaitre X, Zhu D.

Circ Cardiovasc Genet. 2011 Dec;4(6):687-94. doi: 10.1161/CIRCGENETICS.110.959064. Epub 2011 Oct 19.

16.

Kynurenine-transaminase, kynureninase and the increase of xanthurenic acid excretion.

OGASAWARA N, HAGINO Y, KOTAKE Y.

J Biochem. 1962 Sep;52:162-6. No abstract available.

17.

Kynurenine metabolism and xanthurenic acid formation in vitamin B6-deficient rat after tryptophan injection.

Takeuchi F, Tsubouchi R, Izuta S, Shibata Y.

J Nutr Sci Vitaminol (Tokyo). 1989 Apr;35(2):111-22.

PMID:
2732805
19.

[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment].

Grimm U, Knapp A, Machill G, Schmitz W, Smetan M, Schmitz KW, Reddemann H, Schulz M, Schlenzka K.

Acta Biol Med Ger. 1975;34?710:1659-64. German.

PMID:
1233849
20.

Deficiency of fumarylacetoacetase without hereditary tyrosinemia.

Kvittingen EA, Børresen AL, Stokke O, van der Hagen CB, Lie SO.

Clin Genet. 1985 Jun;27(6):550-4.

PMID:
4017276

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