Pages that link to "Q36487020"
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The following pages link to Molecular cloning and nucleotide sequence of human glucocerebrosidase cDNA (Q36487020):
Displaying 50 items.
- Human lysosomal acid phosphatase: cloning, expression and chromosomal assignment (Q24297177) (← links)
- Amino acid sequence of the mRNA cap-binding protein from human tissues (Q24298811) (← links)
- Complete primary structure of human and rabbit lactase-phlorizin hydrolase: implications for biosynthesis, membrane anchoring and evolution of the enzyme (Q24338789) (← links)
- High level transcription of the glucocerebrosidase pseudogene in normal subjects and patients with Gaucher disease (Q24618509) (← links)
- Sequence variability of a human pseudogene (Q24620031) (← links)
- A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorder (Q24624775) (← links)
- Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme (Q24628616) (← links)
- Structure and replication of the genome of the hepatitis delta virus (Q24628855) (← links)
- Human acid beta-glucosidase: isolation and amino acid sequence of a peptide containing the catalytic site (Q24632218) (← links)
- Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region (Q24648974) (← links)
- Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene (Q24676872) (← links)
- High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews (Q24678565) (← links)
- Enzyme replacement in Gaucher disease (Q24796608) (← links)
- Regulation of lysosomal ion homeostasis by channels and transporters (Q28069327) (← links)
- The relationship between glucocerebrosidase mutations and Parkinson disease (Q28077257) (← links)
- Mutations causing Gaucher disease (Q28250128) (← links)
- Lambda ZAP: a bacteriophage lambda expression vector with in vivo excision properties (Q29618268) (← links)
- Non-pseudogene-derived complex acid beta-glucosidase mutations causing mild type 1 and severe type 2 gaucher disease (Q33844209) (← links)
- Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease (Q33894098) (← links)
- Sphingolipid transport in eukaryotic cells. (Q33944782) (← links)
- Gaucher disease: insights from a rare Mendelian disorder (Q34077331) (← links)
- Comparison of the chromosomal localization of murine and human glucocerebrosidase genes and of the deduced amino acid sequences (Q34286863) (← links)
- Production of human glucocerebrosidase in mice after retroviral gene transfer into multipotential hematopoietic progenitor cells (Q34319718) (← links)
- Advances in directed protein evolution by recursive genetic recombination: applications to therapeutic proteins (Q34365192) (← links)
- Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease (Q34386597) (← links)
- The LIMP-2/SCARB2 binding motif on acid β-glucosidase: basic and applied implications for Gaucher disease and associated neurodegenerative diseases (Q34396981) (← links)
- Complete correction of the enzymatic defect of type I Gaucher disease fibroblasts by retroviral-mediated gene transfer (Q34595051) (← links)
- Characterization of mutations in Gaucher patients by cDNA cloning (Q35125664) (← links)
- Gaucher disease: A G 1----A 1 IVS2 splice donor site mutation causing exon 2 skipping in the acid beta-glucosidase mRNA (Q35196039) (← links)
- Gaucher disease: genetic heterogeneity within and among the subtypes detected by immunoblotting (Q35198801) (← links)
- Human acid beta-glucosidase: Northern blot and S1 nuclease analysis of mRNA from HeLa cells and normal and Gaucher disease fibroblasts (Q35199042) (← links)
- The human glucocerebrosidase gene has two functional ATG initiator codons. (Q35199613) (← links)
- Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts (Q35248348) (← links)
- Retroviral-mediated transfer of the human glucocerebrosidase gene into cultured Gaucher bone marrow (Q35604723) (← links)
- Gaucher disease as a paradigm of current issues regarding single gene mutations of humans (Q36353819) (← links)
- The role of glucocerebrosidase mutations in Parkinson disease and Lewy body disorders (Q36486264) (← links)
- Delivery of lysosomal enzymes for therapeutic use: glucocerebrosidase as an example (Q36640336) (← links)
- Theearly andlate processing of lysosomal enzymes: Proteolysis and compartmentation (Q36777557) (← links)
- Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA). (Q37109338) (← links)
- Identification and expression of acid beta-glucosidase mutations causing severe type 1 and neurologic type 2 Gaucher disease in non-Jewish patients (Q37367741) (← links)
- Glucocerebrosidase processing in normal fibroblasts and in fibroblasts from patients with type I, type II, and type III Gaucher disease (Q37402001) (← links)
- Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state (Q37630096) (← links)
- Laboratory and genetic evaluation of Gaucher disease (Q37780488) (← links)
- Acid beta-glucosidase: enzymology and molecular biology of Gaucher disease (Q37832784) (← links)
- How I treat Gaucher disease (Q37889029) (← links)
- Emerging therapeutic targets for Gaucher disease (Q38270518) (← links)
- Translation modulation of acid beta-glucosidase in HepG2 cells: participation of the PKC pathway (Q38330962) (← links)
- Parkinson's disease: acid-glucocerebrosidase activity and alpha-synuclein clearance (Q38727638) (← links)
- Glucosidase acid beta gene mutations in Egyptian children with Gaucher disease and relation to disease phenotypes (Q38988854) (← links)
- Assembly of lysosomes: perspectives from comparative molecular cell biology. (Q39577228) (← links)