Zobrazeno 1 - 10
of 26
pro vyhledávání: '"J. Alexander Lowden"'
Autor:
J. Alexander Lowden
Publikováno v:
North American Actuarial Journal. 3:67-78
Genetic tests are laboratory procedures that identify changes in our genes. Most human disease results, in whole or in part, from alterations in genes. Because the tests are expected to have incredible predictive power and because they may tell us pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09b5afab754e5215dc5e5ed6f6d384bd
https://doi.org/10.1080/10920277.1999.10595775
https://doi.org/10.1080/10920277.1999.10595775
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1199:215-223
Rates of GM2 ganglioside hydrolysis by fibroblasts from normal controls and patients with GM2 gangliosidosis were measured in situ, with cells growing in tissue culture by assaying the decrease in cell-incorporated 3H-GM2 over time, and in vitro by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f48f9865f2e1875c84d364fe7269c0
https://doi.org/10.1016/0304-4165(94)90118-x
https://doi.org/10.1016/0304-4165(94)90118-x
Autor:
J Alexander, Lowden
Publikováno v:
Journal of insurance medicine (New York, N.Y.). 34(1)
The National Cholesterol Education Program has developed a set of guidelines for optimal levels of serum lipids that are recommended to reduce the risk of coronary artery disease. This article compares those values to lipid levels found in insurance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6ba584cb1d760b87aba89f2c4038c68
https://pubmed.ncbi.nlm.nih.gov/15303591
https://pubmed.ncbi.nlm.nih.gov/15303591
Autor:
J Alexander, Lowden
Publikováno v:
Proceedings, the annual meeting of the Medical Section of the American Council of Life Insurance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::458d5377e29d153a7ef98b220e7a2006
https://pubmed.ncbi.nlm.nih.gov/11653009
https://pubmed.ncbi.nlm.nih.gov/11653009
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1243:557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::315ae87334f3decd5f02eac27c6e710d
https://doi.org/10.1016/0304-4165(94)00120-m
https://doi.org/10.1016/0304-4165(94)00120-m
Autor:
J. Alexander Lowden, Anton Novak
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1243:555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35372787fe7ae0cd25b7e69808f16f6
https://doi.org/10.1016/0304-4165(94)00119-i
https://doi.org/10.1016/0304-4165(94)00119-i
Publikováno v:
Canadian Journal of Biochemistry and Cell Biology. 63:723-729
The type and distribution of the oligosaccharides on each polypeptide of human placental β-hexosaminidases A (α(βaβb)) and B (2((βaβb)) were examined. The denatured polypeptides were separated by isoelectric focussing in a polyacrylamide slab g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a8459427e8a588be952054122758402
https://doi.org/10.1139/o85-090
https://doi.org/10.1139/o85-090
Publikováno v:
Canadian Journal of Biochemistry and Cell Biology. 62:529-534
β-Galactosidase purified to apparent homogeneity from human placenta occurred in two separable fractions. A low molecular mass form (relative mass (Mr) 170 000) is composed of a single polypeptide chain (Mr 70 000). This was derived from a larger fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::794f09f0a17afba3d8de7b0a30813fa9
https://doi.org/10.1139/o84-070
https://doi.org/10.1139/o84-070
Publikováno v:
The Journal of Pediatrics. 86:805-809
THIS 8 -YEAR-OLD BOY was n o r m a l u n t i l t h r e e months before admission, when he developed a sore throat and was treated with an unknown antibiotic, after which he became progressively deaf to the spoken word. One and one-half months later h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d43b01b3971e7e669790f56dd899699
https://doi.org/10.1016/s0022-3476(75)80379-9
https://doi.org/10.1016/s0022-3476(75)80379-9
Publikováno v:
Clinical Biochemistry. 18:92-97
Metachromatic leukodystrophy (MLD) presents as six separate variant forms, four allelic and two non-allelic. It is diagnosed in the laboratory by a decrease in the fibroblast or leukocyte arylsulfatase A activity, generally against an artificial subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f04e857c0a7ec266afd721a3b467cde7
https://doi.org/10.1016/s0009-9120(85)80088-6
https://doi.org/10.1016/s0009-9120(85)80088-6