Kamakari S - Search Results

1

Assignment of a human cold shock domain protein A intronless pseudogene (CSDAP1) to human chromosome 16 band p11.2 by in situ hybridization.

Argyrokastritis A, Kontaraki J, Kamakari S, Pasparaki A, Moschonas NK. Argyrokastritis A, et al. Among authors: kamakari s. Cytogenet Cell Genet. 1999;84(1-2):53-4. doi: 10.1159/000015213. Cytogenet Cell Genet. 1999. PMID: 10343102 No abstract available.

2

Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17.

Argyrokastritis A, Kamakari S, Kapsetaki M, Kritis A, Talianidis I, Moschonas NK. Argyrokastritis A, et al. Among authors: kamakari s. Hum Genet. 1997 Feb;99(2):233-6. doi: 10.1007/s004390050345. Hum Genet. 1997. PMID: 9048927

3

Map integration at human chromosome 10: molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map.

Marzella R, Kokkinaki MA, Kapsetaki M, Ricco A, Argyrokastritis A, Kamakari S, Sarafidou T, Archidiacono N, Roussou A, Pasparaki A, Rocchi M, Moschonas NK. Marzella R, et al. Among authors: kamakari s. Cytogenet Cell Genet. 1997;79(3-4):257-65. doi: 10.1159/000134738. Cytogenet Cell Genet. 1997. PMID: 9605867

4

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.

Kamakari S, Thiselton D, Lindsay S, Hardcastle A, Bhattacharya S. Kamakari S, et al. Cytogenet Cell Genet. 1995;71(2):151-4. doi: 10.1159/000134096. Cytogenet Cell Genet. 1995. PMID: 7656586

5

Structural analysis and expression profile of a novel gene on chromosome 5q23 encoding a Golgi-associated protein with six splice variants, and involved within the 5q deletion of a Ph(-) CML patient.

Kamakari S, Roussou A, Jefferson A, Ragoussis I, Anagnou NP. Kamakari S, et al. Leuk Res. 2005 Jan;29(1):17-31. doi: 10.1016/j.leukres.2004.04.019. Leuk Res. 2005. PMID: 15541471

6

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.

Thiselton DL, Lindsay S, Kamakari S, Hardcastle AJ, Roustan P, Bhattacharya SS. Thiselton DL, et al. Among authors: kamakari s. Genomics. 1995 Jan 1;25(1):279-81. doi: 10.1016/0888-7543(95)80136-a. Genomics. 1995. PMID: 7774929

7

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.

Lindsay S, Curtis AR, Roustan P, Kamakari S, Thiselton DL, Stephenson A, Bhattacharya SS. Lindsay S, et al. Among authors: kamakari s. Genomics. 1993 Jul;17(1):208-10. doi: 10.1006/geno.1993.1303. Genomics. 1993. PMID: 8406451

8

Two dinucleotide repeat polymorphisms at the DXS571 locus.

Curtis AR, Roustan P, Kamakari S, Thiselton D, Lindsay S, Bhattacharya SS. Curtis AR, et al. Among authors: kamakari s. Hum Mol Genet. 1992 Dec;1(9):776. doi: 10.1093/hmg/1.9.776. Hum Mol Genet. 1992. PMID: 1302618 No abstract available.

9

Dinucleotide repeat polymorphism at the DXS559 locus.

Roustan P, Curtis AR, Kamakari S, Thiselton D, Lindsay S, Bhattacharya SS. Roustan P, et al. Among authors: kamakari s. Hum Mol Genet. 1992 Dec;1(9):778. doi: 10.1093/hmg/1.9.778. Hum Mol Genet. 1992. PMID: 1302620 No abstract available.

10

X chromosome linkage studies in familial Rett syndrome.

Curtis AR, Headland S, Lindsay S, Thomas NS, Boye E, Kamakari S, Roustan P, Anvret M, Wahlstrom J, McCarthy G, et al. Curtis AR, et al. Among authors: kamakari s. Hum Genet. 1993 Jan;90(5):551-5. doi: 10.1007/BF00217457. Hum Genet. 1993. PMID: 8094068

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