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Results:
1-12
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Results: 12
Authors:
Ugolini, F
Charafe-Jauffret, E
Bardou, VJ
Geneix, J
Adelaide, J
Labat-Moleur, F
Penault-Llorca, F
Longy, M
Jacquemier, J
Birnbaum, D
Pebusque, MJ
Citation: F. Ugolini et al., WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1 in most invasive carcinomas except of the medullary type, ONCOGENE, 20(41), 2001, pp. 5810-5817
Authors:
Longy, M
Citation: M. Longy, Molecular basis of diagnosis in genetics, GASTRO CL B, 25(4), 2001, pp. B14-B17
Authors:
Paraf, F
Gilquin, M
Longy, M
Gilbert, B
Gorry, P
Petit, B
Labrousse, F
Citation: F. Paraf et al., MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non-polyposis colorectal cancer in young patients, HISTOPATHOL, 39(3), 2001, pp. 250-258
Authors:
Bougeard, G
Limacher, JM
Martin, C
Charbonnier, F
Killian, A
Delattre, O
Longy, M
Jonveaux, P
Fricker, JP
Stoppa-Lyonnet, D
Flaman, JM
Frebourg, T
Citation: G. Bougeard et al., Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome, J MED GENET, 38(4), 2001, pp. 253-256
Authors:
Frebourg, T
Ebel, A
Bonaiti-Pellie, C
Brugieres, L
Berthet, P
Bressac-De Paillerets, B
Chevrier, A
Chompret, A
Cohen-Haguenauer, O
Delattre, O
Feingold, J
Feunteun, J
Frappaz, D
Fricker, JP
Gesta, P
Jonveaux, P
Kalifa, C
Lasset, C
Leheup, B
Limacher, JM
Longy, M
Nogues, C
Oppenheim, D
Sommelet, D
Soubrier, F
Stoll, C
Stoppa-Lyonnet, D
Tristant, H
Citation: T. Frebourg et al., Li-Fraumeni syndrome: update, new data and guidelines for clinical management, B CANCER, 88(6), 2001, pp. 581-587
Authors:
Bonneau, D
Longy, M
Citation: D. Bonneau et M. Longy, Mutations of the human PTEN gene, HUM MUTAT, 16(2), 2000, pp. 109-122
Authors:
Frengen, E
Rocca-Serra, P
Shaposhnikov, S
Taine, L
Thorsen, J
Bepoldin, C
Krekling, M
Lafon, D
Aas, KK
Abd El Moneim, A
Johansen, H
Longy, M
Prydz, H
Dorion-Bonnet, F
Citation: E. Frengen et al., High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1, GENOMICS, 70(3), 2000, pp. 273-285
Authors:
Leprat, F
Bonichon, F
Guyot, M
Trouette, H
Trojani, M
Vergnot, V
Longy, M
Belleannee, G
de Mascarel, A
Roger, P
Citation: F. Leprat et al., Familial non-medullary thyroid carcinoma: pathology review in 27 affected cases from 13 French families, CLIN ENDOCR, 50(5), 1999, pp. 589-594
Authors:
Longy, M
Citation: M. Longy, The Muir-Torre syndrome, ANN DER VEN, 126(8-9), 1999, pp. 580-581
Authors:
Lauge, A
Lefebvre, C
Laurent-Puig, P
Caux, V
Gad, S
Eng, C
Longy, M
Stoppa-Lyonnet, D
Citation: A. Lauge et al., No evidence for germline PTEN mutations in families with breast and brain tumours, INT J CANC, 84(3), 1999, pp. 216-219
Authors:
Zhou, XP
Li, YJ
Hoang-Xuan, K
Laurent-Puig, P
Mokhtari, K
Longy, M
Sanson, M
Delattre, JY
Thomas, G
Hamelin, R
Citation: Xp. Zhou et al., Mutational analysis of the PTEN gene in gliomas: Molecular and pathological correlations, INT J CANC, 84(2), 1999, pp. 150-154
Authors:
Feilotter, HE
Coulon, V
McVeigh, JL
Boag, AH
Dorion-Bonnet, F
Duboue, B
Latham, WCW
Eng, C
Mulligan, LM
Longy, M
Citation: He. Feilotter et al., Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma, BR J CANC, 79(5-6), 1999, pp. 718-723
Risultati:
1-12
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