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Selected Publication:

Auner, HW; Olipitz, W; Hoefler, G; Bodner, C; Konrad, D; Crevenna, R; Linkesch, W; Sill, H.
Mutational analysis of the DNA mismatch repair gene hMLH1 in myeloid leukaemias.
Br J Haematol. 1999; 106(3):706-708 Doi: 10.1046%2Fj.1365-2141.1999.01595.x [OPEN ACCESS]
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Leading authors Med Uni Graz
Sill Heinz
Co-authors Med Uni Graz
Höfler Gerald
Linkesch Werner
Olipitz Werner
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Abstract:
Mutations of the DNA mismatch repair (MMR) gene hMLH1 have recently been linked to the development of some hereditary and sporadic cancers which frequently display widespread microsatellite instability (MSI). Conflicting results regarding the extent of MSI in myeloid leukaemias prompted us to perform mutational analysis of all 19 exons of the hMLH1 gene by polymerase chain reaction-single-stranded conformation polymorphism (PCR-SSCP) and sequence analysis in a total of 133 patients with acute and chronic myeloid leukaemia. Apart from one exonic and one intronic polymorphism, no mutations were detected in any of the samples indicating that the major MMR gene hMLH1 is not involved in the pathogenesis or progression of myeloid malignancies.
Find related publications in this database (using NLM MeSH Indexing)
Acute Disease -
Base Pair Mismatch -
Carrier Proteins -
Chronic Disease -
DNA Repair -
Humans -
Leukemia, Myeloid - genetics
Microsatellite Repeats - genetics
Mutation - genetics
Neoplasm Proteins - genetics
Nuclear Proteins - genetics
Polymerase Chain Reaction - methods

Find related publications in this database (Keywords)
Acute Myeloid Leukemia
Chronic Myeloid Leukemia
DNA Mismatch Repair
Hmlh1
Microsatellite Instability
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