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1. 先天性および後天性鉄芽球性貧血の原因 causes of congenital and acquired sideroblastic anemias
2. チロシン代謝障害 disorders of tyrosine metabolism
3. ALA脱水酵素欠損性ポルフィリン症 ala dehydratase porphyria
4. ポルフィリン症：概要 porphyrias an overview
5. 光線角化症の治療 treatment of actinic keratosis

English Journal

Novel A219P Mutation of Hydroxymethylbilane Synthase Identified in a Chinese Woman with Acute Intermittent Porphyria and Syndrome of Inappropriate Antidiuretic Hormone.

Li Y1, Qu H1, Wang H1, Deng H1, Liu Z2.
Annals of human genetics.Ann Hum Genet.2015 Jul;79(4):310-2. doi: 10.1111/ahg.12107. Epub 2015 Mar 18.
Acute intermittent porphyria (AIP) is an autosomal dominant metabolic disorder caused by deficiency of the heme biosynthetic enzyme hydroxymethylbilane synthase (approved gene symbol HMBS), also known as porphobilinogen deaminase (PBGD). AIP is characterised by intermittent attacks of abdominal pain
PMID 25787008

Liver Transplantation for Acute Intermittent Porphyria: Biochemical and Pathologic Studies of the Explanted Liver.

Yasuda M1, Erwin AL1, Liu LU2, Balwani M1,2, Chen B1, Kadirvel S1, Gan L1, Fiel MI3, Gordon RE3, Yu C1, Clavero S1, Arvelakis A4, Naik H1, Martin LD5, Phillips JD6, Anderson KE7, Sadagoparamanujam VM7, Florman SS2,4, Desnick RJ1.
Molecular medicine (Cambridge, Mass.).Mol Med.2015 Jun 5. doi: 10.2119/molmed.2015.00099. [Epub ahead of print]
Acute intermittent porphyria (AIP) is an autosomal dominant hepatic disorder caused by the half-normal activity of hydroxymethylbilane synthase (HMB-synthase). Symptomatic individuals experience life-threatening acute neurovisceral attacks that are precipitated by factors that induce the hepatic exp
PMID 26062020

Expression and functional role of the prorenin receptor in the human adrenocortical zona glomerulosa and in primary aldosteronism.

Recarti C1, Seccia TM, Caroccia B, Gonzales-Campos A, Ceolotto G, Lenzini L, Petrelli L, Belloni AS, Rainey WE, Nussberger J, Rossi GP.
Journal of hypertension.J Hypertens.2015 May;33(5):1014-22. doi: 10.1097/HJH.0000000000000504.
OBJECTIVES: Prorenin can be detected in plasma of hypertensive patients. If detected in patients with primary aldosteronism could implicate prorenin in the development of primary aldosteronism. To address this issue, we measured the plasma prorenin levels in primary aldosteronism patients, the expre
PMID 25668351

Japanese Journal

Effect of cadmium binding form on rabbit aminolevulinate dehydratase in high molecular weight fraction of rainbow trout liver

JIA Huijuan,REN Huifeng,ENDO Hideaki,HAYASHI Tetsuhito
Fisheries science : FS 76(3), 495-501, 2010-05-01
NAID 10026450096

Acute Diphenyl Diselenide Treatment Reduces Hyperglycemia But Does Not Change Delta-Aminolevulinate Dehydratase Activity in Alloxan-Induced Diabetes in Rats(Biochemistry)

BARBOSA Nilda Berenice de Vargas,OLIVEIRA Caroline,ARALDI Dioneia,FOLMER Vanderlei,ROCHA Joao Batista Teixeira,NOGUEIRA Cristina Wayne
Biological & pharmaceutical bulletin 31(12), 2200-2204, 2008-12-01
… However, the delta-aminolevulinate dehydratase (δ-ALA-D) activity inhibited by alloxan was not restored by diphenyl diselenide. …
NAID 110007005015

Related Pictures

Rat Alad(Aminolevulinate Delta DehydRatase) ELISA Kit - FineTest ELISA Kit | FineTest Relationship between delta-aminolevulinic acid dehydratase (d-ALAD) | Download 5-aminolevulinate synthetase; Acid Synthetase, Aminolevulinic; Acid Synthetase, delta Porphobilinogen synthase; Aminolevulinate Hydro-Lyase; Aminolevulinic Acid Dehydratase 5-Amino Laevulinate Dehydratase

★リンクテーブル★

リンク元	「アミノレブリン酸デヒドラターゼ」
拡張検索	「5-aminolevulinate dehydratase」
関連記事	「dehydratase」「aminolevulinate」