KSIĄŻKI POWIĄZANE ZE SŁOWEM «SULPHATASE»
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1
Comparative Animal Biochemistry
Because of the frequent overlapping of the substrate specificity of individual
enzymes, this classification must be considered provisional; the real relationships
between the sulphatase types cannot be determined in the absence of sequence
...
2
The Biochemistry of Inorganic Compounds of Sulphur
deficient not only in sulphatase A and sulphatase B but also in sulphatase C. The
deficiency of sulphatase A, however, seems to be a constant factor. This work is
the first demonstration of an alteration in the level of a specific sulphatase in a ...
A. B. Roy, P. A. Trudinger, 1970
3
the biochemistry of enorganic compounds of sulphur
deficient not only in sulphatase A and sulphatase B but also in sulphatase C. The
deficiency of sulphatase A, however, seems to be a constant factor. This work is
the first demonstration of an alteration in the level of a specific sulphatase in a ...
4
Mycobacterium: Genomics and Molecular Biology
The sequence information given for M. avium stf5 and stf6 from mycobacterial
sulphatase analysis study (Mougous et al., 2002a) does not match with the open
reading frames in the annotated-M. avium genome; therefore, the genome ...
Tanya Parish, Amanda Claire Brown, 2009
5
Chemistry and Biology of Heparin and Heparan Sulfate
Human liver iduronate2-sulphatase. Purification, characterization and catalytic
properties. Biochem J 1990; 271:75-86. Wilson PJ, Morris CP, Anson DS,
Occhiodoro T, Bielicki J , Clements PR, Hopwood JJ. Hunter syndrome: isolation
of an ...
Hari G. Garg, Robert J. Linhardt, Charles A. Hales, 2011
6
Genetic Disorders and the Fetus: Diagnosis, Prevention and ...
The metabolic and molecular bases of inherited disease, 8th edn. New York:
McGraw-Hill, 2001:3725. 255. Vamos E, Liebaers l, Bousard N, Libert J,
Perlmutter N. Multiple sulphatase deficiency with early onset. J Inherit Metab Dis
1981;4:103.
Aubrey Milunsky, Jeff Milunsky, 2011
7
Greenfield's Neuropathology, 2-Volume Set, Eighth Edition
Iduronate sulphatase Oetc. O S 1 O O S H2COH H2COH O COOH COOH O O
NAc NAc O O H2COH H2COH COOH O α-L-Iduronidase Oetc. S O O 2 O H2COH
COOH COOH O NAc NAc O O H2COH O O Oetc. O 3 O NAc NAc OO O SO (a) ...
Seth Love, David Louis, David W Ellison, 2008
8
A Dictionary of Biomedicine
Aryl sulphatase A (EC 3.1.6.1, 507 aa) is a lysosomal enzyme that hydrolyses
cerebroside 3-sulphate and is deficient in *metachromatic leucodystrophy. Aryl
sulphatase B (N-acetylgalactosamine 4-sulphatase, EC 3.1.6.12, 533 aa) is
involved ...
John Lackie, Christopher O'Callaghan, 2010
9
Metabolic Breakdown of Steroids: Volume 2: Book II on ...
They believe that the body must contain an enzyme capable of hydrolysing this
conjugated (estrogen and obtained some evidence for the presence of a
sulphatase in rat liver homogenates. . CALLOWZ I should have wondered
whether you ...
CIBA Foundation Symposium, 2009
10
The Climacteric: An Update
Oestrone sulphatase is a membranebound enzyme. Moreover clinical
observation 3 has confirmed that the sulphatase activity does not vary inrelation
to themenstrualcycle, that the activityincreases in patientswithan irregular
cycleandthat ...
H. Herendael, B. Herendael, F. E. Riphagen, 1984
WIADOMOŚCI, KTÓRE ZAWIERAJĄ SŁOWO «SULPHATASE»
Sprawdź, o czym dyskutuje się w prasie krajowej i zagranicznej oraz jak jest stosowane słowo
sulphatase w wiadomościach.
Double the reasons to celebrate at The Acorns
At the event was 18-year-old Pavan Tailor who has a Multiple Sulphatase Deficiency and has used the services of Acorns at its hospice in Birmingham for 15 ... «www.solihullnews.net, Gru 14»
Izzy's Mission
Izzy has a rare form of this disease, Multiple Sulphatase Deficiency (MSD), which further complicates the treatment, and course of the disease. It is not known ... «The Jewish Press, Gru 13»
libragen contributes to success of PolyModE
As a result of this combined approach, 10 novel sulphatase producers were identified from more than 20000 screened metagenomic clones and the partners ... «News-Medical.net, Paz 13»
Trial watch: Enzyme replacement success in Phase III trial for rare …
In MPS-IVA there is a deficiency in galactosamine-6-sulphatase, an enzyme that is responsible for degradation of the keratan sulphate that is normally found in ... «Nature.com, Sty 13»
