SCOPUS 정보 검색 플랫폼

Volumn 94, Issue 1, 2008, Pages 139-

In vivo specific reduction of arylsulfatase B enzymatic activity in children with cystic fibrosis

(9) Ferrero, Giovanni Battista a Pagliardini, Severo b Veljkovic, Aleksandar b Porta, Francesco a Bena, Cristina a Tardivo, Irene b Restagno, Gabriella b Silengo, Margherita Cirillo a Bignamini, Elisabetta b

a UNIVERSITY OF TURIN (Italy)

b REGINA MARGHERITA CHILDREN S HOSPITAL (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GALACTOSIDASE; N ACETYLGALACTOSAMINE 4 SULFATASE;

ACIDIFICATION; CHILD; CONTROLLED STUDY; CYSTIC FIBROSIS; ENZYME ACTIVITY; GENOTYPE; HUMAN; IN VIVO STUDY; LETTER; LEUKOCYTE; LUNG FIBROSIS; LYSOSOME; MAJOR CLINICAL STUDY; NEWBORN SCREENING; PEDIATRICS; PRIORITY JOURNAL; REDUCTION KINETICS;

CHILD; CYSTIC FIBROSIS; HUMANS; N-ACETYLGALACTOSAMINE-4-SULFATASE;

EID: 41949086906 PISSN: 10967192 EISSN: 10967206 Source Type: Journal
DOI: 10.1016/j.ymgme.2007.10.010 Document Type: Letter

Times cited : (13)

References (5)

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2
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- Increased arylsulfatase B activity in cystic fibrosis cells following correction of CFTR
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3
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- Does deficiency of arylsulfatase B have a role in cystic fibrosis?
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- Tobacman, J.K.¹

4
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- High incidence of later-onset Fabry disease revealed by newborn screening
- Spada M., Pagliardini S., Yasuda M., Tukel T., Thiagarajan G., Sakuraba H., Ponzone A., and Desnick R.J. High incidence of later-onset Fabry disease revealed by newborn screening. Am. J. Hum. Genet. 79 (2006) 31-40
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5
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- CFTR regulates phagosome acidification in macrophages and alters bactericidal activity
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.