क्यूआर कोड

Quantitation of a Urinary Profile of Biomarkers in Gaucher Disease Type 1 Patients Using Tandem Mass Spectrometry

Gaucher disease is a rare inherited disorder caused by a deficiency of the lysosomal acid beta-glucocerebrosidase enzyme. Metabolomic studies by our group targeted several new potential urinary biomarkers. Apart from lyso-Gb<sub>1</sub>, these studies highlighted lyso-Gb<sub>1</sub> analogs −28, −26...

पूर्ण विवरण

में बचाया:
मुख्य लेखकों: Iskren Menkovic, Michel Boutin, Abdulfatah Alayoubi, Filipa Curado, Peter Bauer, François E. Mercier, Christiane Auray-Blais
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: MDPI AG 2022-06-01
श्रृंखला:Diagnostics
विषय:
Gaucher disease type 1
urine
biomarkers
glucosylsphingosine
lyso-Gb<sub>1</sub>
lyso-Gb<sub>1</sub> analogs
ऑनलाइन पहुंच:https://www.mdpi.com/2075-4418/12/6/1414
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