Zobrazeno 1 - 10
of 338
pro vyhledávání: '"L, Denoroy"'
Publikováno v:
Journal of Chemical Neuroanatomy. 11:131-142
The adrenergic phenotype was analysed in the rat's rostral dorsomedial medulla under normal conditions and 3 days after a single intraperitoneal injection of an eburnamine derivative, RU 24722, which increases tyrosine hydroxylase protein expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41e4c2925f55b2f23984cbca5b4955f
https://doi.org/10.1016/0891-0618(96)00152-4
https://doi.org/10.1016/0891-0618(96)00152-4
Publikováno v:
Diabetologia. 39:135-141
Anti-diabetic sulphonylureas act via high affinity binding sites coupled to K-ATP channels. Endosulfine, an endogenous ligand for these binding sites, was shown to exist in two molecular forms, alpha and beta, in both the pancreas and the central ner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2315d29d714e16643c403122160fe64
https://doi.org/10.1007/bf00403955
https://doi.org/10.1007/bf00403955
Publikováno v:
Neonatology. 65:189-193
Some dysmaturity of neuroregulator neuronal systems may be responsible for brain stem disorders. These disorders may partly explain the mechanism of death in SIDS. The available data using microbiochemical assays, immunocytochemical techniques and au
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96a05498622f828beb8f654c73aa7ba5
https://doi.org/10.1159/000244051
https://doi.org/10.1159/000244051
Autor:
N Dalla Venezia, Jean Delaunay, A Forissier, J Besalduch, M Aymerich, Nicole Alloisio, JL Vives Corrons, L Denoroy, I. Besson
Publikováno v:
Blood. 82:1661-1665
We present two Spanish children with hereditary elliptopoikilocytosis. The mother displayed a symptomless elliptocytosis. Spectrin maps showed the alpha I/50–46b abnormality in the mother and in the children. The change was more conspicuous in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55df160cebe16507cb715d5f9a150968
https://doi.org/10.1182/blood.v82.5.1661.bloodjournal8251661
https://doi.org/10.1182/blood.v82.5.1661.bloodjournal8251661
Autor:
J Maréchal, Jean Delaunay, Z Benhadji Zouaoui, Nicole Alloisio, C Feo, R Wilmotte, L Denoroy, P Texier
Publikováno v:
Blood. 81:2791-2798
Spectrin Oran (alpha II/21) has been reported previously as a variant of the alpha II domain. Its expression level is low (10% of total spectrin) in heterozygotes denoting a major disadvantage of the mutated alpha-chain dimer or tetramer with respect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbb27b500baa3aac0fbb0c9837fa208
https://doi.org/10.1182/blood.v81.10.2791.bloodjournal81102791
https://doi.org/10.1182/blood.v81.10.2791.bloodjournal81102791
Publikováno v:
Annals of Neurology. 33:357-367
We used immunohistochemical analysis to determine whether medulla oblongata neurons containing phenylethanolamine N-methyltransferase (PNMT) are affected in patients who died with idiopathic Parkinson's disease (n = 7) compared with age-matched contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83659bbfd7704b2fe4a44551ef5a4856
https://doi.org/10.1002/ana.410330405
https://doi.org/10.1002/ana.410330405
Publikováno v:
Neuropediatrics. 24:25-29
Immunohistochemical study of catecholamine synthesizing enzymes tyrosine hydroxylase (TH) and phenylethanolamine-N-methyl transferase (PNMT) was performed in lower brain stem of 5 controls and 9 sudden infant death "syndrome" (SIDS) cases. No differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3c9e8b6cee1ed8bf155ba9fb161cbc4
https://doi.org/10.1055/s-2008-1071508
https://doi.org/10.1055/s-2008-1071508
Autor:
J Maréchal, L Morle, MT Ducluzeau, R Kastally, C Feo, Nicole Alloisio, L Denoroy, R Wilmotte, Jean Delaunay, Faouzi Baklouti, BG Forget
Publikováno v:
Blood. 80:809-815
Spectrin Jendouba (alpha II/31) was found in a Tunisian family. In the heterozygous state, it is associated with asymptomatic elliptocytosis and a minimal defect in spectrin dimer self-association. On partial digestion of spectrin with trypsin, an ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::792cb00efa8e96bd3640759c2e5ba8c1
https://doi.org/10.1182/blood.v80.3.809.809
https://doi.org/10.1182/blood.v80.3.809.809
Autor:
Jean Delaunay, MH Ben Aribia, Nicole Alloisio, R Kastally, Faouzi Baklouti, MT Ducluzeau, A Mrad, J Maréchal, R Wilmotte, L Morle, L Denoroy
Publikováno v:
Blood. 79:2464-2470
Elliptocytogenic alpha I/36 spectrin Sfax is a new variant found in a Tunisian family. The alpha I/36 allele yielded a clinically manifest picture only when occurring in trans to a recently identified, low expression level polymorphism referred to as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01059c5c0a7a32146669375212d8286b
https://doi.org/10.1182/blood.v79.9.2464.2464
https://doi.org/10.1182/blood.v79.9.2464.2464
Autor:
Alain Sarrieau, Jacques Epelbaum, Fatiha Chigr, D. Jordan, Mohamed Najimi, A. de Broca, L. Denoroy, William Rostène, N. Kopp
Publikováno v:
Neurochemistry International. 20:113-118
Quantitative autoradiography analysis of neurotensin (NT) and somatostatin (SS) binding sites was performed on coronal sections of the medulla oblongata from 2 fetuses, 6 controls and 7 victims of Sudden Infant Death Syndrome (SIDS). Throughout the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da9d46beb484fc2f7b2280f9ebcaf463
https://doi.org/10.1016/0197-0186(92)90134-d
https://doi.org/10.1016/0197-0186(92)90134-d