Zobrazeno 1 - 10
of 137
pro vyhledávání: '"J C Penhos"'
Autor:
J C, PENHOS
Publikováno v:
La Semana medica. 54(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::afa06cf98de21884e844a3ad680ac35b
https://pubmed.ncbi.nlm.nih.gov/20342246
https://pubmed.ncbi.nlm.nih.gov/20342246
Autor:
J C, PENHOS
Publikováno v:
La Semana medica. 54(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad9037feb1a303cb7212f521624ecb5a
https://pubmed.ncbi.nlm.nih.gov/20239621
https://pubmed.ncbi.nlm.nih.gov/20239621
Publikováno v:
Transplantation. 49(5)
The growth-inhibitory effect of prednisone is a serious drawback to its use in kidney graft recipients. At high doses, cyclosporine also inhibits somatic growth in animals. Furthermore, cyclosporine, in addition to being nephrotoxic in patients, is r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c06b69fc1fc99e98980358f99917eed5
https://pubmed.ncbi.nlm.nih.gov/2336703
https://pubmed.ncbi.nlm.nih.gov/2336703
Publikováno v:
Annals of the New York Academy of Sciences. 71:25-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e11a6f049aef84147284af0386ece71
https://doi.org/10.1111/j.1749-6632.1975.tb46725.x
https://doi.org/10.1111/j.1749-6632.1975.tb46725.x
Publikováno v:
Prostaglandins. 21:699-705
1. 1. Pharmacologic doses of hydrocortisone sodium succinate (100 mg/kg) has a rapid protective action against arachidonate-induced mortality in mice when administered intravenously 5 to 60 min before intravenous infusion of arachidonate. 2. 2. Intra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df5778b21cd516ff2609c7a1f17fe21
https://doi.org/10.1016/0090-6980(81)90227-6
https://doi.org/10.1016/0090-6980(81)90227-6
Publikováno v:
Experimental Biology and Medicine. 148:1159-1163
SummaryA new technique is described for evisceration in the rat in which liver function is preserved. These animals lack all known sources of glucagon and insulin and are capable of active gluconeogenesis, urea formation and ketone body production by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22dab08327ec13d11cd9af0463325e7e
https://doi.org/10.3181/00379727-148-38708
https://doi.org/10.3181/00379727-148-38708
Publikováno v:
Annals of the New York Academy of Sciences. 71:12-24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19f43b83eec3570d3bf4770f8fbf96ed
https://doi.org/10.1111/j.1749-6632.1975.tb46724.x
https://doi.org/10.1111/j.1749-6632.1975.tb46724.x
Publikováno v:
Diabetologia. 14:177-184
Eviscerated rats (animals without gastrointestinal tract or pancreas, but with intact liver and kidneys) are diabetic with blood glucose levels of 287 ± 10 mg% (n = 35) 24 h after surgery. Immunoreactive insulin (IRI) and immunoreactive glucagon (IR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda65a245274bceb003805becbe043d2
https://doi.org/10.1007/bf00429778
https://doi.org/10.1007/bf00429778
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 239:E346-E353
Surgical removal of the jejunum, ileum, and colon from rats (LBX) results in greatly elevated levels of plasma immunoreactive glucagon (pIRG) 24 h after surgery (0.98 +/- 0.07 ng/ml, n = 51 vs. 0.20 +/- 0.02 ng/ml, n = 34 in sham-operated controls).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6631c8ebff5d604055b07c7cd924c4c
https://doi.org/10.1152/ajpendo.1980.239.5.e346
https://doi.org/10.1152/ajpendo.1980.239.5.e346
Publikováno v:
Diabetes. 24:637-640
Fed male Wistar rats were eviscerated by two procedures. The first group of eviscerated rats were left with a nonfunctional liver in situ while the second group were eviscerated by a newer technic, developed in this laboratory, that preserves liver f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f633557ef1f8040e32be6ce8d90bf26
https://doi.org/10.2337/diabetes.24.7.637
https://doi.org/10.2337/diabetes.24.7.637