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Kimérizmusvizsgálatok jelentősége allogén hematopoetikus őssejt-transzplantációt követően

Significance of chimerism testing following allogeneic hematopoietic stem cell transplantation

Hematológia–Transzfuziológia
Authors:
Nóra Meggyesi
,
Hajnalka Andrikovics
,
András Kozma
,
András Bors
,
Lívia Varga
,
Zoltán Őrfi
,
László Gopcsa
,
Melinda Paksi
,
Éva Torbágyi
,
Nóra Lovas
,
Marienn Réti
,
Gergely Kriván
,
István Vályi-Nagy
, and
Péter Reményi

JR, Scott SD, Jack AL, et al.: Monitoring of chimerism following allogeneic haematopoietic stem cell transplantation (HSCT): technical recommendations for the use of short tandem repeat (STR) based techniques

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A case of disputed paternity in dogs is reported. DNA examinations were carried out from hair samples of the individuals several months after the death of the putative sire. Ten short tandem repeat (STR) loci were analysed by fluorescence- labelled multiplex PCR using ABI PRISM 310 Genetic Analyser. Based on the results the candidate sire was included in the pedigree records as the biological sire. In spite o f the genetic homogeneity of pedigree dogs due to inbreeding, canine microsatellites can provide an adequate basis for assigning paternity in pure breeds.

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Orvosi Hetilap
Authors:
Lilla Lakner
,
Veronika Csöngei
,
Lili Magyari
,
Márta Varga
,
Pál Miheller
,
Patrícia Sarlós
,
Péter Orosz
,
Zsolt Bári
,
István Takács
,
Luca Járomi
,
Enikő Sáfrány
,
Csilla Sipeky
,
Judit Bene
,
Zsolt Tulassay
,
Zoltán Döbrönte
, and
Béla Melegh

-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers. Hum. Mutat., 2005, 25 , 156–166. Funke A. A

Open access

A ritka kromoszóma-rendellenességek és a fetoplacentaris mozaikosság jelentősége a praenatalis diagnosztikában a nem invazív szűrővizsgálatok tükrében

The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis in the non-invasive prenatal testing era

Orvosi Hetilap
Authors:
Zsolt Tidrenczel
,
Erika P. Tardy
,
Ildikó Böjtös
,
Edina Sarkadi
,
Judit Simon
,
Henriett Pikó
,
Gábor Vermes
,
János Demeter
, and
Artúr Beke

] 4 Findlay I, Tóth T, Matthews P, et al. Rapid trisomy diagnosis (21, 18, and 13) using fluorescent PCR and short tandem repeats: applications for prenatal diagnosis and preimplantation genetic

Open access
Orvosi Hetilap
Authors:
Zsolt Tidrenczel
,
Erika P. Tardy
,
Henriett Pikó
,
Edina Sarkadi
,
Ildikó Böjtös
,
János Demeter
,
P. János Kósa
, and
Artúr Beke

, 18, and 13) using fluorescent PCR and short tandem repeats: applications for prenatal diagnosis and preimplantation genetic diagnosis. J Assist Reprod Genet. 1998; 15: 266–275. 9

Open access
Acta Microbiologica et Immunologica Hungarica
Authors:
Gábor Görcsös
,
László Irinyi
,
László Radócz
,
Gábor Tarcali
, and
Erzsébet Sándor

, C. : Mutation of human short tandem repeats . Hum Mol Genet 2 , 1123 – 1128 ( 1993 ). 38. Schug , M. D. , Mackay , T. F. C. , Aquadro , C. F. : Low mutation rates

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Allogén HSCT után a kimérizmus monitorozása az igazságügyi orvostanban is alkalmazott egyénazonosító technikával, short tandem repeat módszerrel történik, melynek érzékenysége >1%. Ahogy a mérhető reziduális betegség (MRD) vizsgálata betegségspecifikus

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