15 results for author:"Maillet P." in Literature citations
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| BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families. Cherbal F., Salhi N., Bakour R., Adane S., Boualga K., Maillet P. Dis. Markers 32:343-353(2012) · Mapped (18) |
| BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families. Cherbal F., Bakour R., Adane S., Boualga K., Benais-Pont G., Maillet P. Dis. Markers 28:377-384(2010) · Mapped (18) |
| International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation. Peixoto A., Santos C., Pinheiro M., Pinto P., Soares M.J., Rocha P., Gusmao L., Amorim A., van der Hout A., Gerdes A.M. et al. Breast Cancer Res. Treat. 127:671-679(2011) · Mapped (18) |
| Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases. Novak D.J., Sabbaghian N., Maillet P., Chappuis P.O., Foulkes W.D., Tischkowitz M. Breast Cancer Res. Treat. 117:453-459(2009) · UniProtKB (2) · Mapped (2) |
| The contribution of germline rearrangements to the spectrum of BRCA2 mutations. Casilli F., Tournier I., Sinilnikova O.M., Coulet F., Soubrier F., Houdayer C., Hardouin A., Berthet P., Sobol H., Bourdon V. et al. J. Med. Genet. 43:e49-e49(2006) · Mapped (18) |
| Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients. Russell A.M., Zhang J., Luz J., Hutter P., Chappuis P.O., Berthod C.R., Maillet P., Mueller H., Heinimann K. Int. J. Cancer 118:1937-1940(2006) · Mapped (13) |
| Protein 4.1R expression in normal and dystrophic skeletal muscle. Delhommeau F., Dalla Venezia N., Moriniere M., Collin H., Maillet P., Guerfali I., Leclerc P., Fardeau M., Delaunay J., Baklouti F. C. R. Biol. 328:43-56(2005) · Mapped (8) |
| Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis. Alloisio N., Texier P., Vallier A., Ribeiro M.L., Morle L., Bozon M., Bursaux E., Maillet P., Goncalves P., Tanner M.J. et al. Blood 90:414-420(1997) · UniProtKB (1) |
| Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus. Miraglia del Giudice E., Vallier A., Maillet P., Perrotta S., Cutillo S., Iolascon A., Tanner M.J., Delaunay J., Alloisio N. Br. J. Haematol. 96:70-76(1997) · UniProtKB (1) |
| Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis. Maillet P., Alloisio N., Morle L., Delaunay J. Hum. Mutat. 8:97-107(1996) · UniProtKB (2) |
| Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas). Alloisio N., Maillet P., Carre G., Texier P., Vallier A., Baklouti F., Philippe N., Delaunay J. Blood 88:1062-1069(1996) · Mapped (11) |
| Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11. Maillet P., Vallier A., Reinhart W.H., Wyss E.J., Ott P., Texier P., Baklouti F., Tanner M.J.A., Delaunay J., Alloisio N. Br. J. Haematol. 91:804-810(1995) · UniProtKB (1) |
| Complete amino acid sequence of a human platelet proteoglycan. Alliel P.M., Perin J.-P., Maillet P., Bonnet F., Rosa J.-P., Jolles P. FEBS Lett. 236:123-126(1988) · UniProtKB (1) |
| Characterization and N-terminal sequence of human platelet proteoglycan. Perin J.-P., Bonnet F., Maillet P., Jolles P. Biochem. J. 255:1007-1013(1988) · UniProtKB (1) |
| Characterization of a human seminal plasma glycosaminoglycan-bearing polypeptide. Bonnet F., Perin J.-P., Maillet P., Jolles P., Alliel P.M. Biochem. J. 288:565-569(1992) · UniProtKB (1) |