Literature DB >> 4768898

Isolation and characterization of glucocerebrosidase from human placental tissue.

P G Pentchev, R O Brady, S R Hibbert, A E Gal, D Shapiro.   

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Year:  1973        PMID: 4768898

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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  33 in total

1.  Benefits from unearthing "a biochemical Rosetta Stone".

Authors:  Roscoe O Brady
Journal:  J Biol Chem       Date:  2010-10-28       Impact factor: 5.157

2.  Enzyme replacement therapy in Gaucher's disease: preliminary clinical trial of a new enzyme preparation.

Authors:  E Beutler; G L Dale; D E Guinto; W Kuhl
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

Review 3.  Glycosphingolipid hydrolases: properties and molecular genetics.

Authors:  M Wan Ho; A G Norden; J A Alhadeff; J S O'Brien
Journal:  Mol Cell Biochem       Date:  1977-10-07       Impact factor: 3.396

4.  Enzyme replacement and gene therapy for Gaucher's disease.

Authors:  R O Brady; N W Barton
Journal:  Lipids       Date:  1996-03       Impact factor: 1.880

5.  Rapid partial purification of placental glucocerebroside beta-glucosidase and its entrapment in liposomes.

Authors:  I P Braidman; G Gregoriadis
Journal:  Biochem J       Date:  1977-05-15       Impact factor: 3.857

Review 6.  Lysosomal enzyme replacement therapies: Historical development, clinical outcomes, and future perspectives.

Authors:  Melani Solomon; Silvia Muro
Journal:  Adv Drug Deliv Rev       Date:  2017-05-11       Impact factor: 15.470

Review 7.  Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923-2016).

Authors:  Markus Ries
Journal:  J Inherit Metab Dis       Date:  2017-03-17       Impact factor: 4.982

Review 8.  Modifying exogenous glucocerebrosidase for effective replacement therapy in Gaucher disease.

Authors:  R O Brady; G J Murray; N W Barton
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

9.  [Glucocerebrosidase deficiency and tentative identification of heterozygous carriers in a family with Gaucher's disease type I (author's transl)].

Authors:  K Harzer
Journal:  Klin Wochenschr       Date:  1974-12-15

10.  Review of the safety and efficacy of imiglucerase treatment of Gaucher disease.

Authors:  Deborah Elstein; Ari Zimran
Journal:  Biologics       Date:  2009-09-15
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