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A GENE ADJACENT TO SATELLITE DNA IN DROSOPHILA MELANOGASTERCARLSON M; BRUTLAG D.1978; PROC. NATION. ACAD. SCI. U.S.A.; USA; DA. 1978; VOL. 75; NO 12; PP. 5898-5902; BIBL. 29 REF.Article

CLUSTERS CONTAINING DIFFERENT MOBILE DISPERSED GENES IN THE GENOME OF DROSOPHILA MELANOGASTERTCHURIKOV NA; ZELENTSOVA ES; GEORGIEV GP et al.1980; NUCLEIC ACIDS RES.; GBR; DA. 1980; VOL. 8; NO 6; PP. 1243-1258; BIBL. 17 REF.Article

Identification of restriction fragment length polymorphism and random amplified polymorphic DNA markers linked to downy mildew resistance genes in lettuce, using near-isogenic linesPARAN, I; KESSELI, R; MICHELMORE, R et al.Genome (Ottawa. Print). 1991, Vol 34, Num 6, pp 1021-1027, issn 0831-2796Article

Histological characterization of resistant in Lactuca saligna to lettuce downy mildew (Bremia lactucae)LEBEDA, A; REININK, K.Physiological and molecular plant pathology. 1994, Vol 44, Num 2, pp 125-139, issn 0885-5765Article

Development of reliable PCR-based markers linked to downy mildew resistance genes in lettucePARAN, I; MICHELMORE, R. W.Theoretical and Applied Genetics. 1993, Vol 85, Num 8, pp 985-993, issn 0040-5752Article

Detection of a premutation in Japanese myotonic dystrophyYAMAGATA, H; MIKI, T; JOHNSON, K et al.Human molecular genetics (Print). 1994, Vol 3, Num 5, pp 819-820, issn 0964-6906Article

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal alleleHOFMANN-RADVANYI, H; LAVEDAN, C; RABES, J.-P et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, pp 1263-1266, issn 0964-6906Article

An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3LENNON, G. G; LAMERDIN, J; LIEUALLEN, K et al.Human molecular genetics (Print). 1992, Vol 1, Num 3, issn 0964-6906, p. 217Article

MspI RFLP at 19q12-q13.1 identified by the anonymous DNA sequence p20B18 [D19S30]SMEETS, H; SCHEPENS, J; COERWINKEL, M et al.Nucleic acids research. 1989, Vol 17, Num 8, issn 0305-1048, 3323 [1 p.]Article

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyANVRET, M; ÅHLBERG, G; GRANDELL, U et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, pp 1397-1400, issn 0964-6906Article

MspI RFLP at 19cen-q12 identified by the anonymous DNA sequence pPM17.4 [D19S29]SMEETS, H; MARKSLAG, P; HULSEBOS, T et al.Nucleic acids research. 1989, Vol 17, Num 8, issn 0305-1048, 3324 [1 p.]Article

TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28]SMEETS, H; SCHEPENS, J; COERWINKEL, M et al.Nucleic acids research. 1989, Vol 17, Num 8, issn 0305-1048, 3325 [1 p.]Article

A novel repeat structure at the myotonic dystrophy locus in a 37 repeat allele with unexpectedly high stabilityLEEFLANG, E. P; ARNHEIM, N.Human molecular genetics (Print). 1995, Vol 4, Num 1, pp 135-136, issn 0964-6906Article

Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) geneJANSEN, G; COERWINKEL-DRIESSEN, M; NILLESEN, W et al.Human molecular genetics (Print). 1993, Vol 2, Num 3, issn 0964-6906, p. 333Article

Myotonic dystrophy mutation : an unstable CTG repeat in the 3' untranslated region of the geneMAHADEVAN, M; TSILFIDIS, C; LEBLOND, S et al.Science (Washington, D.C.). 1992, Vol 255, Num 5049, pp 1253-1255, issn 0036-8075Article

cDNA surveying of specific tissue expression of human chromosome 19 sequencesDUNNE, P. W; SHANG-WU WANG; ASHIZAWA, T et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 2, pp 263-269, issn 0888-7543Article

Localization of trinucleotide repeat sequences in myotonic dystrophy cells using a single fluorochrome-labeled PNA probeTANEJA, K. L.BioTechniques. 1998, Vol 24, Num 3, pp 472-476, issn 0736-6205Article

LES NOUVEAUX GENES DU CMH (TAP, LMP ET DM) : POLYMORPHISME, COMPATIBILITE ET ASSOCIATION AVEC LE REJET CELLULAIRE EN TRANSPLANTATION RENALE = THE NEW MHC ENCODED GENES (TAP, LMP AND DM) : POLYMORPHISM, COMPATIBILITY AND ASSOCIATION WITH ACUTE CELLULAR REJECTION IN KIDNEY TRANSPLANTATIONChevrier, Dominique; Muller, Jean-Yves.1997, 150 p.Thesis

A molecular protocol for diagnosing myotonic dystrophyGUIDA, M; MARGER, R. S; PAPP, A. C et al.Clinical chemistry (Baltimore, Md.). 1995, Vol 41, Num 1, pp 69-72, issn 0009-9147Conference Paper

High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutationNEVILLE, C. E; MAHADEVAN, M. S; BARCELO, J. M et al.Human molecular genetics (Print). 1994, Vol 3, Num 1, pp 45-51, issn 0964-6906Article

Identification of variable simple sequence motifs in 19q13.2-qter : markers for the myotonic dystrophy locusSMEETS, H. J. M; HERMENS, R; BRUNNER, H. G et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 2, pp 257-263, issn 0888-7543, 7 p.Article

Myotonic dystrophy rewied: back to the future?WIERINGA, B.Human molecular genetics (Print). 1994, Vol 3, Num 1, pp 1-7, issn 0964-6906Article

Structure and genomic sequence of the myotonic dystrophy (DM kinase) geneMAHADEVAN, M. S; AMENIYA, C; DE JONG, P et al.Human molecular genetics (Print). 1993, Vol 2, Num 3, pp 299-304, issn 0964-6906Article

Les genes TAP, LMP et DM : une contribution a l'étude du polymorphisme = Studies of polymorphism in TAP, LMP and DM genesMoins Teisserenc, Helene; Charron, Dominique.1997, 145 p.Thesis

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesJANSEN, G; BARTOLOMEI, M; KALSCHEUER, V et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, pp 1221-1227, issn 0964-6906Article

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