Výsledky vyhledávání - "C M, Castiglione"

Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia

Autor: K S, Chang, J M, Trujillo, T, Ogura, C M, Castiglione, K K, Kidd, S R, Zhao, E J, Freireich, S A, Stass

Publikováno v: Leukemia. 5(3)

The retinoic acid receptor-alpha (RAR-alpha) gene was previously localized to chromosome 17q21, a region close to the t(15;17) (q22;q21) abnormality in acute promyelocytic leukemia (APL). We used the RAR-alpha gene as a probe and found that eight of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::65c1ddf6b68e7eb8af4cae6b27225e06
https://pubmed.ncbi.nlm.nih.gov/1849600

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The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10

Autor: J S, Wu, N L, Carson, S, Myers, A J, Pakstis, J R, Kidd, C M, Castiglione, L, Anderson, L S, Hoyle, M, Genel, M, Verdy

Publikováno v: American journal of human genetics. 46(3)

Multiple endocrine neoplasia type 2A (MEN2A) is a rare cancer syndrome that is inherited in an apparently autosomal dominant fashion. Previous linkage studies had assigned the MEN2A locus to chromosome 10 in the pericentromeric region. We recently ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::193e16cc31a5b725b4f2e4bbae6225a5
https://pubmed.ncbi.nlm.nih.gov/1968709

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Polymorphism of the human c-abl gene: relation to incidence and course of chronic myelogenous leukemia

Autor: L, Daniel, C M, Ahmed, R S, Bloodgood, J R, Kidd, C M, Castiglione, S, Duttagupta, P, Lebowitz

Publikováno v: Oncogene. 1(2)

Abnormalities in structure and expression of the proto-oncogene c-abl have been implicated in the genesis of chronic myelogenous leukemia (CML). We studied leukemic cell DNA from 42 CML patients for evidence of rearrangement and/or amplification of c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7dea35e0c5dde58e21eb7c9c25c5f309
https://pubmed.ncbi.nlm.nih.gov/2894000

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Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion region

Autor: K K, Kidd, J R, Kidd, C M, Castiglione, A J, Pakstis, R S, Sparkes

Publikováno v: Genetic epidemiology. 3(3)

In an earlier paper, positive but nonsignificant lod scores were found in pair-wise linkage tests between multiple endocrine neoplasia type 2A (MEN-2A) and both the haptoglobin (HP) locus on chromosome 16 and group-specific component (GC) locus on ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b70d4b6364d867b43379d1c9aeac5d20
https://pubmed.ncbi.nlm.nih.gov/2873080

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One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map

Autor: A J, Pakstis, J R, Kidd, C M, Castiglione, B A, Pletcher, P D, Murphy, L A, Farrer, M, Genel, K K, Kidd

Publikováno v: Henry Ford Hospital medical journal. 35(2-3)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::520a424540b2ca1ec0746faa71b4a5fc
https://pubmed.ncbi.nlm.nih.gov/2891651

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The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1

Autor: K K, Kidd, J R, Kidd, C M, Castiglione, R S, Sparkes, J A, Egeland, E, Bakker

Publikováno v: Human heredity. 38(1)

D1S2 was one of the first restriction fragment length polymorphisms (RFLPs) assigned to chromosome 1, but its regional location was unknown. In this paper we present data that place this RFLP into both the genetic map and the physical-cytogenetic map

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d6c79c716d1a1953fc857d3209ddd1c7
https://pubmed.ncbi.nlm.nih.gov/2895061

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