Zobrazeno 1 - 10
of 20
pro vyhledávání: '"P E, Purdue"'
Publikováno v:
Hydrology and Earth System Sciences, Vol 18, Iss 4, Pp 1369-1382 (2014)
When simulating social action in modeling efforts, as in socio-hydrology, an issue of obvious importance is how to ensure that social action by human agents is well-represented in the analysis and the model. Generally, human decision-making is either
Externí odkaz:
https://doaj.org/article/c5e7e5e0b4ef452ca4849b44a04839d9
Publikováno v:
Clinical Orthopaedics and Related Research. 454:251-261
The generation of prosthetic implant wear after total joint arthroplasty is recognized as the major initiating event in development of periprosthetic osteolysis and aseptic loosening, the leading complication of this otherwise successful surgical pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0893fb321d5751f88a4906d7a5b85b85
https://doi.org/10.1097/01.blo.0000238813.95035.1b
https://doi.org/10.1097/01.blo.0000238813.95035.1b
Autor:
Zhenxin Shen, Kevin P. McHugh, P E Purdue, Merrilee R. Flannery, Regina P. O'Sullivan, Steven R. Goldring, Tania N. Crotti
Publikováno v:
Annals of the Rheumatic Diseases. 69:i83-i85
Analysis of tissues retrieved from the bone-pannus interface from patients with rheumatoid arthritis (RA) and studies in animal models of inflammatory arthritis provide strong evidence that osteoclasts, the cells that are essential for physiological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea1b8d929b52ffcf433a75f976a0b502
https://doi.org/10.1136/ard.2009.120188
https://doi.org/10.1136/ard.2009.120188
Publikováno v:
Neurochemical Research. 24:581-586
Rhizomelic chondrodysplasia punctata (RCDP) is a lethal autosomal recessive disease corresponding to complementation group 11 (CG11), the second most common of the thirteen CGs of peroxisomal biogenesis disorders (PBDs). RCDP is characterized by prox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee86de6325adee5f39c9a92ebebfc53b
https://doi.org/10.1023/a:1023957110171
https://doi.org/10.1023/a:1023957110171
Autor:
P E Purdue, Paul B. Lazarow
Publikováno v:
The Journal of Cell Biology
We have identified a novel peroxisomal targeting sequence (PTS) at the extreme COOH terminus of human catalase. The last four amino acids of this protein (-KANL) are necessary and sufficient to effect targeting to peroxisomes in both human fibroblast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2123f37db1c60fab9557895355b666eb
https://doi.org/10.1083/jcb.134.4.849
https://doi.org/10.1083/jcb.134.4.849
Autor:
Paul B. Lazarow, P E Purdue
Publikováno v:
Journal of Biological Chemistry. 269:30065-30068
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eca7882541e3f000b511f8d4c0650343
https://doi.org/10.1016/s0021-9258(18)43771-4
https://doi.org/10.1016/s0021-9258(18)43771-4
Publikováno v:
Human Genetics. 94:55-64
The autosomal recessive disease primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver-specific peroxisomal enzyme alanine:glyoxylate amino-transferase (AGT). This paper concerns the identification, characterization and clinical us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04adb5c580262fa335999d9dadb371d
https://doi.org/10.1007/bf02272842
https://doi.org/10.1007/bf02272842
Publikováno v:
Journal of Inherited Metabolic Disease. 17:487-499
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by a deficiency of the liver-specific peroxisomal enzyme alanine: glyoxylate aminotransferase (AGT). The disease is notable for its extensive heterogeneity at the clinical, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d25f1157e9ea383ec099b2efbaa6a54e
https://doi.org/10.1007/bf00711363
https://doi.org/10.1007/bf00711363
Publikováno v:
The Plant Journal. 2:763-773
Two maize genes and cDNAs encoding the mitochondrial adenine nucleotide translocator (ANT), a nuclear-encoded inner mitochondrial membrane carrier protein, have previously been isolated in this laboratory. Sequence analysis revealed the existence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d8467173d46ab3ede1874e53332264
https://doi.org/10.1046/j.1365-313x.1992.t01-15-00999.x
https://doi.org/10.1046/j.1365-313x.1992.t01-15-00999.x
Publikováno v:
Proceedings of the National Academy of Sciences. 88:10900-10904
In approximately one-third of primary hyperoxaluria type 1 patients, disease is associated with a unique protein sorting defect in which hepatic L-alanine:glyoxylate aminotransferase (AGT; EC 2.6.1.44), which is normally peroxisomal, is mistargeted t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac806d0b83421b05d3247f4d7fa39dc
https://doi.org/10.1073/pnas.88.23.10900
https://doi.org/10.1073/pnas.88.23.10900