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Assignment of the programmed cell death 4 gene (PDCD4) to human chromosome band 10q24 by in situ hybridizationSOEJIMA, H; MIYOSHI, O; YOSHINAGA, H et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 113-114, issn 0301-0171Article

Terminal deletion of the long arm of chromosome 10SCIGLIANO, S; GREGOIRE, M. J; SCHMITT, M et al.Clinical genetics. 2004, Vol 65, Num 4, pp 294-298, issn 0009-9163, 5 p.Article

RING CHROMOSOME 10: 46, XX, R (10) (P15->Q26)TSUKINO R; TSUDA N; DEZAWA T et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 2; PP. 148-151; BIBL. 4 REF.Article

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26CICHON, S; SCHMIDT-WOLF, G; FRITZE, J et al.Molecular psychiatry. 2001, Vol 6, Num 3, pp 342-349, issn 1359-4184Article

Mapping of the human ribosomal small subunit protein gene RPS24 to the chromosome 10q22-q23 boundaryJONES, A.-M; MARZELLA, R; ROCCHI, M et al.Genomics (San Diego, Calif.). 1997, Vol 39, Num 1, pp 121-122, issn 0888-7543Article

Assignment of the closet human homologue (DNA2L; KIAA0083) of the yeast Dna2 helicase gene to chromosome band 10q21.3-q22.1EKI, T; OKUMURA, K; SHIRATORI, A et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 3, pp 408-410, issn 0888-7543Article

Assignment of the human β-microseminoprotein gene (MSMB) to chromosome 10q11.2SASAKI, T; MATSUMOTO, N; JINNO, Y et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 177-178, issn 0301-0171Conference Paper

Assignment of the human prosaposin gene (PSAP) to 10q22.1 by fluorescence in situ hybridizationBAR-AM, I; AVIVI, L; HOROWITZ, M et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 4, pp 316-318, issn 0301-0171Conference Paper

RING CHROMOSOME 10 ASSOCIATED WITH MULTIPLE CONGENITAL MALFORMATIONSSIMONI G; ROSSELLA F; DALPRA L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 117-121; BIBL. 8 REF.Article

Interstitial deletion del(10)(q25.2q25.3 ∼ 26.11) : case report and review of the literatureKEHRER-SAWATZKI, Hildegard; DAUMILLER, Eva; MÜLLER-NAVIA, Jutta et al.Prenatal diagnosis. 2005, Vol 25, Num 10, pp 954-959, issn 0197-3851, 6 p.Article

Localization of the gene (TAF2D) encoding the 100-kDa subunit (hTAFII100) of the human TFIID complex to chromosome 10 band q24-q25.2DUBROVSKAYA, V; MATTEI, M.-G; TORA, L et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 3, pp 556-557, issn 0888-7543Article

BALANCED TRANSMISSION OF CENTROMERIC FISSION PRODUCTS IN MANFRYNS JP; BULCKE J; HENS L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 127-128; BIBL. 7 REF.Article

RING 10 CHROMOSOME: 46, XX, R10 (P15 Q26)SPARKES RS; LING SM; MULLER H et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 341-345; BIBL. 16 REF.Article

Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanomaGULDBERG, P; THOR STRATEN, P; BIRCK, A et al.Cancer research (Baltimore). 1997, Vol 57, Num 17, pp 3660-3663, issn 0008-5472Article

HTRA1 promoter polymorphism in wet age-related macular degenerationDEWAN, Andrew; MUGEN LIU; BARNSTABLE, Colin et al.Science (Washington, D.C.). 2006, Vol 314, Num 5801, pp 989-992, issn 0036-8075, 4 p.Article

Chromosomal mapping of cell death proteases CPP32, MCH2, and MCH3BULLRICH, F; FERNANDES-ALNEMRI, T; LITWACK, G et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 2, pp 362-365, issn 0888-7543Article

Susceptibility genes for age-related maculopathy on chromosome 10q26JAKOBSDOTTIR, Johanna; CONLEY, Yvette P; WEEKS, Daniel E et al.American journal of human genetics. 2005, Vol 77, Num 3, pp 389-407, issn 0002-9297, 19 p.Article

Improving the comparative map of porcine chromosome 10 with respect to human chromosomes 1, 9 and 10ALDENHOVEN, J; CHEN, Y; BACKOFEN, B et al.Cytogenetic and genome research. 2003, Vol 102, Num 1-4, pp 121-127, issn 1424-8581, 7 p.Article

Transmission ratio distortion in females on chromosome 10p11-p15PATERSON, A. D; PETRONIS, A.American journal of medical genetics. 1999, Vol 88, Num 6, pp 657-661, issn 0148-7299Article

A polymorphism in intron 6 of the CYP17 geneCROCITTO, L. E; FEIGELSON, H. S; YU, M. C et al.Clinical genetics. 1997, Vol 52, Num 1, pp 68-69, issn 0009-9163Article

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolutionCHENG, Jill; KAPRANOV, Philipp; SEMENTCHENKO, Victor et al.Science (Washington, D.C.). 2005, Vol 308, Num 5725, pp 1149-1154, issn 0036-8075, 6 p.Article

PTEN and MXI1 allelic loss on chromosome 10q is rare in melanoma in vivoHERBST, R. A; PODEWSKI, E. K; MOMMERT, S et al.Archives of dermatological research (Print). 1999, Vol 291, Num 10, pp 567-569, issn 0340-3696Article

Assignment of the human ADP-ribosylation factor-like 3 (ARL3) gene to chromosome 10 band q23.3 by radiation hybrid mappingKIM, H.-S.Cytogenetics and cell genetics. 1998, Vol 83, Num 3-4, issn 0301-0171, p. 246Conference Paper

Assignment of human genes for β2 and β4 subunits of voltage-dependent Ca2+ channels to chromosomes 10p12 and 2q22-q23TAVIAUX, S; WILLIAMS, M. E; HARPOLD, M. M et al.Human genetics. 1997, Vol 100, Num 2, pp 151-154, issn 0340-6717Article

Assignment of the human gene encoding the Δ1-pyrroline-5-carboxylate synthetase (P5CS) to 10q24.3 by in situ hybridizationLIU, G; MAUNOURY, C; KAMOUN, P et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 1, pp 145-146, issn 0888-7543Article

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