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Results: 1-19 |
Results: 19
A new family of compounds with tetrahedral anions: PbnBiOn(XO4), X = V, P,As, n=1, 2, 4. A comparison with lead oxysulfates PbnPbOn(SO4)
Authors: Giraud, S Mizrahi, A Drache, M Conflant, P Wignacourt, JP Steinfink, H
Citation: S. Giraud et al., A new family of compounds with tetrahedral anions: PbnBiOn(XO4), X = V, P,As, n=1, 2, 4. A comparison with lead oxysulfates PbnPbOn(SO4), SOLID ST SC, 3(5), 2001, pp. 593-602
Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients
Authors: Niccoli-Sire, P Murat, A Rohmer, V Franc, S Chabrier, G Baldet, L Maes, B Savagner, F Giraud, S Bezieau, S Kottler, ML Morange, S Conte-Devolx, B
Citation: P. Niccoli-sire et al., Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients, J CLIN END, 86(8), 2001, pp. 3746-3753
Translation initiation of the insulin-like growth factor I receptor mRNA is mediated by an internal ribosome entry site
Authors: Giraud, S Greco, A Brink, M Diaz, JJ Delafontaine, P
Citation: S. Giraud et al., Translation initiation of the insulin-like growth factor I receptor mRNA is mediated by an internal ribosome entry site, J BIOL CHEM, 276(8), 2001, pp. 5668-5675
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?
Authors: Martin-Denavit, T Duthel, S Giraud, S Olschwang, S Saurin, JC Plauchu, H
Citation: T. Martin-denavit et al., Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?, CLIN GENET, 60(2), 2001, pp. 125-131
Association of medullary sponge kidney disease and multiple endocrine neoplasia type IIA due to RET gene mutation: is there a causal relationship?
Authors: Diouf, B Ka, EF Calender, A Giraud, S Moreira, T Diop, TM
Citation: B. Diouf et al., Association of medullary sponge kidney disease and multiple endocrine neoplasia type IIA due to RET gene mutation: is there a causal relationship?, NEPH DIAL T, 15(12), 2000, pp. 2062-2063
Molecular characterization of germline NF2 gene rearrangements
Authors: Legoix, P Sarkissian, HD Cazes, L Giraud, S Sor, F Rouleau, GA Lenoir, G Thomas, G Zucman-Rossi, J
Citation: P. Legoix et al., Molecular characterization of germline NF2 gene rearrangements, GENOMICS, 65(1), 2000, pp. 62-66
Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease
Authors: Richard, S David, P Marsot-Dupuch, K Giraud, S Beroud, C Resche, F
Citation: S. Richard et al., Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease, NEUROSURG R, 23(1), 2000, pp. 1-22
On the existence of Bi6.67O4 (XO4)(4) and PbBi6O4 (XO4)(4) (X = P,V, and As)
Authors: Giraud, S Drache, M Conflant, P Wignacourt, JP Steinfink, H
Citation: S. Giraud et al., On the existence of Bi6.67O4 (XO4)(4) and PbBi6O4 (XO4)(4) (X = P,V, and As), J SOL ST CH, 154(2), 2000, pp. 435-443
Crystal structure of Pb5Bi18P4O42: A fluorite-related superstructure
Authors: Giraud, S Wignacourt, JP Swinnea, S Steinfink, H Harlow, R
Citation: S. Giraud et al., Crystal structure of Pb5Bi18P4O42: A fluorite-related superstructure, J SOL ST CH, 151(2), 2000, pp. 181-189
Neuroendocrine tumors and von Hipple-Lindau disease: three cases
Authors: Aubert-Petit, G Baudin, E Cailleux, AF Pellegriti, G Elias, D Travagli, JP Giraud, S Richard, S Schlumberger, M
Citation: G. Aubert-petit et al., Neuroendocrine tumors and von Hipple-Lindau disease: three cases, PRESSE MED, 28(23), 1999, pp. 1231-1234
The stereochemical effect of 6s(2) lone-pair electrons: The crystal structure of a new lead bismuth oxyphosphate Pb4BiO4PO4
Authors: Giraud, S Wignacourt, JP Drache, M Nowogrocki, G Steinfink, H
Citation: S. Giraud et al., The stereochemical effect of 6s(2) lone-pair electrons: The crystal structure of a new lead bismuth oxyphosphate Pb4BiO4PO4, J SOL ST CH, 142(1), 1999, pp. 80-88
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma
Authors: Pigny, P Bauters, C Wemeau, JL Houcke, ML Crepin, M Caron, P Giraud, S Calender, A Buisine, MP Kerckaert, JP Porchet, N
Citation: P. Pigny et al., A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma, J CLIN END, 84(5), 1999, pp. 1700-1704
Mammalian small stress proteins protect against oxidative stress through their ability to increase glucose-6-phosphate dehydrogenase activity and by maintaining optimal cellular detoxifying machinery
Authors: Preville, X Salvemini, F Giraud, S Chaufour, S Paul, C Stepien, G Ursini, MV Arrigo, AP
Citation: X. Preville et al., Mammalian small stress proteins protect against oxidative stress through their ability to increase glucose-6-phosphate dehydrogenase activity and by maintaining optimal cellular detoxifying machinery, EXP CELL RE, 247(1), 1999, pp. 61-78
Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies
Authors: Bonod-Bidaud, C Giraud, S Mandon, G Mousson, B Stepien, G
Citation: C. Bonod-bidaud et al., Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies, EXP CELL RE, 246(1), 1999, pp. 91-97
NF2 gene in neurofibromatosis type 2 patients
Authors: Zucman-Rossi, J Legoix, P Der Sarkissian, H Cheret, G Sor, F Bernardi, A Cazes, L Giraud, S Ollagnon, E Lenoir, G Thomas, G
Citation: J. Zucman-rossi et al., NF2 gene in neurofibromatosis type 2 patients, HUM MOL GEN, 7(13), 1998, pp. 2095-2101
Low temperature epitaxial growth of Si on Si(111) by gas-source MBE with heat-pulse annealing
Authors: Ishikawa, T Okumura, H Akane, T Sano, M Giraud, S Nakabayashi, Y Matsumoto, S
Citation: T. Ishikawa et al., Low temperature epitaxial growth of Si on Si(111) by gas-source MBE with heat-pulse annealing, THIN SOL FI, 336(1-2), 1998, pp. 232-235
Clinical genetic study of MEN1: recent pathophysiological data and clinical applications
Authors: Calender, A Giraud, S Porchet, N Gaudray, P Cadiot, G Mignon, M
Citation: A. Calender et al., Clinical genetic study of MEN1: recent pathophysiological data and clinical applications, ANN ENDOCR, 59(6), 1998, pp. 444-451
von Hippel-Lindau (VHL) disease: recent progress in genetics and patient management
Authors: Richard, S Giraud, S Beroud, C Caron, J Penfornis, F Baudin, E Niccoli-Sire, P Murat, A Schlumberger, M Plouin, PF Conte-Devolx, B
Citation: S. Richard et al., von Hippel-Lindau (VHL) disease: recent progress in genetics and patient management, ANN ENDOCR, 59(6), 1998, pp. 452-458
RET, hereditary cancers and congenital malformation: A deregulation model of a tyrosine kinase receptor in human pathology
Authors: Pasini, A Chappuis-Flament, S Geneste, O Fournier, L Schuffenecker, I Michiels, FM Feunteun, J Pelet, A Lyonnet, S De Vita, G Santoro, M Lenoir, GM Giraud, S Billaud, M
Citation: A. Pasini et al., RET, hereditary cancers and congenital malformation: A deregulation model of a tyrosine kinase receptor in human pathology, EUROCANCER 98, 1998, pp. 95-96
Risultati: 1-19 |