WordNet

an impairment of health or a condition of abnormal functioning
street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
having the characteristics of an acid; "an acid reaction"
(computer science) the process of storing information in a computer memory or on a magnetic tape or disk
the act of storing something
the commercial enterprise of storing goods and materials
of or relating to infants or infancy; "infantile paralysis"
being or befitting or characteristic of an infant; "infantile games"
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

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1. ペリツェウス・メルツバッハー病 pelizaeus merzbacher disease
2. 先天性代謝異常：分類 inborn errors of metabolism classification
3. 先天性代謝異常：疫学、病因、および臨床的特徴 inborn errors of metabolism epidemiology pathogenesis and clinical features

A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.

Chung YK1, Sohn YB, Sohn JM, Lee J, Chang MS, Kwun Y, Kim CH, Lee JY, Yook YJ, Ko AR, Jin DK.
Glycoconjugate journal.Glycoconj J.2014 May;31(4):309-15. doi: 10.1007/s10719-014-9523-0. Epub 2014 Apr 30.
Mucopolysaccharidosis II (MPS II, Hunter syndrome; OMIM 309900) is an X-linked lysosomal storage disease caused by a deficiency in the enzyme iduronate-2-sulfatase (IDS), leading to accumulation of glycosaminoglycans (GAGs). For enzyme replacement therapy (ERT) of Hunter syndrome, two recombinant en
PMID 24781369

Extraction and immobilization of SA-α-2,6-Gal receptors on magnetic nanoparticles to study receptor stability and interaction with Sambucus nigra lectin.

Gregorio-Jauregui KM1, Carrizalez-Alvarez SA, Rivera-Salinas JE, Saade H, Martinez JL, López RG, Segura EP, Ilyina A.
Applied biochemistry and biotechnology.Appl Biochem Biotechnol.2014 Apr;172(8):3721-35. doi: 10.1007/s12010-014-0801-x. Epub 2014 Feb 25.
The interaction between influenza virus hemagglutinins and host cell with terminal sialic acid linked receptors, SA-α-2,6-Gal for human strains is important to obtain insights into this infectious disease. Sambucus nigra lectin has high affinity for SA-α-2,6-Gal receptors. The goals of this work w
PMID 24566927

GM1-gangliosidosis in American black bears: clinical, pathological, biochemical and molecular genetic characterization.

Muthupalani S1, Torres PA2, Wang BC2, Zeng BJ2, Eaton S3, Erdelyi I1, Ducore R1, Maganti R1, Keating J1, Perry BJ1, Tseng FS4, Waliszewski N4, Pokras M4, Causey R5, Seger R5, March P6, Tidwell A6, Pfannl R7, Seyfried T3, Kolodny EH8, Alroy J9.
Molecular genetics and metabolism.Mol Genet Metab.2014 Apr;111(4):513-21. doi: 10.1016/j.ymgme.2014.02.002. Epub 2014 Feb 13.
G(M1)-gangliosidosis is a rare progressive neurodegenerative disorder due to an autosomal recessively inherited deficiency of lysosomal β-galactosidase. We have identified seven American black bears (Ursus americanus) found in the Northeast United States suffering from G(M1)-gangliosidosis. This re
PMID 24581871

Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder

Ishiwari Kouhei,Kotani Masaharu,Suzuki Minoru [他],Pumbo E,Suzuki A,Kobayashi T,Ueno T,Fukushige T,Kanzaki T,Imada M,Itoh K,Akioka S,Tajima Y,Sakuraba H
Journal of human genetics 49(12), 656-663, 2004-12-01
NAID 10014226137

Infantile sialic acid storage disease (ISSD) : Report of the first case detected in Poland

TYLKI-SZYMANSKA ANNA,CZARTORYSKA BARBARA,LUGOWSKA AGNIESZKA,VERHEIJEN FRANS W,MANCINI GRAZIA M S,ROKICKI DARIUSZ,TAYBERT JOANNA,CHMIELINSKA ELZBIETA
Pediatrics international : official journal of the Japan Pediatric Society 45(2), 199-200, 2003-04-01
NAID 10011917227