Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Y. M. Choy"'
Publikováno v:
Diseases, Vol 7, Iss 3, p 47 (2019)
Although individually uncommon, rare diseases collectively account for a considerable proportion of disease impact worldwide. A group of rare genetic diseases called the mucopolysaccharidoses (MPSs) are characterized by accumulation of partially degr
Externí odkaz:
https://doaj.org/article/f7f96be005d5498bb01a8380bdbb3e61
Publikováno v:
Diseases, Vol 5, Iss 1, p 6 (2017)
Ease of design, relatively low cost and a multitude of gene-altering capabilities have all led to the adoption of the sophisticated and yet simple gene editing system: clustered regularly interspaced short palindromic repeats/CRISPR-associated protei
Externí odkaz:
https://doaj.org/article/4111967f769448d09dfb07a0a4664fb9
Autor:
Francis Y. M. Choy, Tessa N. Campbell
Publikováno v:
International Journal of Cell Biology, Vol 2011 (2011)
Gaucher disease is an inherited disorder caused by a deficiency in the lysosomal hydrolase glucocerebrosidase. There is a wide spectrum of clinical presentations, with the most common features being hepatosplenomegaly, skeletal disease, and cytopenia
Externí odkaz:
https://doaj.org/article/7e2d42bcf645453e9f1097a5cd3cf0f7
Publikováno v:
Journal of International Medical Research. 22:299-312
Many Chinese medicinal plants have immunomodulatory and anti-tumour activities. Most of the anti-tumour activities of these Chinese herbs are probably due to their immunostimulating polysaccharide components. A general scheme for the isolation and pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4b3c4545b1832af3d4d95f7d1d4fcf
https://doi.org/10.1177/030006059402200601
https://doi.org/10.1177/030006059402200601
Publikováno v:
Clinical Genetics. 61:229-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4481dc9df959be6be758ba689bd650b9
https://doi.org/10.1034/j.1399-0004.2002.610312.x
https://doi.org/10.1034/j.1399-0004.2002.610312.x
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2d82985228809b7631cc202cbf466e0
https://doi.org/10.1002/chin.199510297
https://doi.org/10.1002/chin.199510297
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aba026a86f6c11dccd0ca1b315775f4b
https://doi.org/10.1002/chin.199701250
https://doi.org/10.1002/chin.199701250
Publikováno v:
Current issues in molecular biology. 12(3)
Since its discovery in 1979, p53 has become the focus of intensive cancer-based research in laboratories around the world. The p53 protein mediates critical cellular functions including the response to genotoxic stress, differentiation, senescence, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d6d83daf9c934ad61d1581ba2e7b406
https://pubmed.ncbi.nlm.nih.gov/19918091
https://pubmed.ncbi.nlm.nih.gov/19918091
Publikováno v:
American Journal of Medical Genetics. 41:469-474
Gaucher disease, the most prevalent lysosomal storage disease, is an autosomal recessive sphingolipidosis resulting from deficient glucocerebrosidase activity. Genomic DNA of the structural gene of glucocerebrosidase from normal individuals and fifte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a11e3dbce0e92fd1383d0feaa719df75
https://doi.org/10.1002/ajmg.1320410418
https://doi.org/10.1002/ajmg.1320410418
Publikováno v:
Protein and peptide letters. 13(4)
We examined the production and secretion of fusion constructs containing alpha-N-acetylglucosaminidase, the enzyme deficient in Sanfilippo B, and either wildtype TAT or modified TAT in cultured Spodoptera frugiperda cells. All constructs exhibited su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f46e60c25284b39c8a11dd184bdfc9e2
https://pubmed.ncbi.nlm.nih.gov/16712510
https://pubmed.ncbi.nlm.nih.gov/16712510