戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 r injections in the cat model of human alpha-mannosidosis.
2 cDNA isolated from a goat affected with beta-mannosidosis.
3 (derived from normal marrow) in feline alpha-mannosidosis.
4 cal or pathological progression of the alpha-mannosidosis.
5    Deficiency of this enzyme results in beta-mannosidosis, a lysosomal storage disease characterized
6                                        Alpha-mannosidosis (AMD) is an autosomal recessive prototypica
7 his mouse model closely resembles human beta-mannosidosis and provides a useful tool for studying the
8 ection in a large brain model of human alpha-mannosidosis by intravascular gene therapy', by Yoon et
9                                Treated alpha-mannosidosis cats had reduced severity of neurological s
10 and that obligate carriers in a caprine beta-mannosidosis colony were heterozygous.
11  two siblings differently affected with beta-mannosidosis demonstrated a homozygous A-->G transition
12 arides, oligosaccharides isolated from alpha-mannosidosis fibroblasts, and p-nitrophenyl-alpha-D-mann
13 in all human tissues tested, including alpha-mannosidosis fibroblasts, while minor transcripts of 3.6
14 tem cell transplantation in alpha- and beta- mannosidosis, fucosidosis, and the mucopolysaccharidoses
15 valuated in the large animal models of alpha-mannosidosis, globoid cell leukodystrophy, GM1 and GM2 g
16 utation that is associated with caprine beta-mannosidosis has been identified.
17                                   Human beta-mannosidosis is an autosomal recessive, lysosomal storag
18 ation among the reported cases of human beta-mannosidosis is variable, even among members of the same
19 d by off-target effects, which produce alpha-mannosidosis-like symptoms.
20 erism in a goat with an atypically mild beta-mannosidosis phenotype.
21                                In human beta-mannosidosis, the clinical presentation is variable and
22 n, confirmed that animals affected with beta-mannosidosis were homozygous for the mutation and that o
23 of the human lysosomal storage disease alpha-mannosidosis, which has globally distributed lysosomal s