Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alenka Erjavec Škerget"'
Publikováno v:
Anali PAZU. 3:95-103
Kvantitativna fluorescentna verižna reakcija s polimerazo (QF-PCR) je uveljavljena metoda za usmerjeno, hitro, zanesljivo in poceni določanje najpomembnejših kromosomskih anomalij v prenatalni diagnostiki. To so trisomije kromosomov 13, 18 in 21,
Publikováno v:
Anali PAZU. 1:62-66
Kvantitativna verižna reakcija s polimerazo (QF-PCR) z uporabo markerjev specifičnih za kratka ponavljajoča se zaporedja (STR-short tandem repeat), značilna za določen kromosom, je uspešna metoda za hitro diagnosticiranje najpogostejših kromos
Autor:
Špela Stangler Herodež, Nastja Stankovič, Boris Zagradišnik, Alenka Erjavec Škerget, Nadja Kokalj Vokač
Publikováno v:
Acta Medico-Biotechnica. 6:47-52
Purpose: The VKORC1 polymorphism is an important genetic factor affecting warfarin dose requirement. Patients require different warfarin doses in order to achieve the target therapeutic anticoagulation. The aim of our study was to determine the frequ
Autor:
Boris Zagradišnik, Špela Stangler Herodež, Alenka Erjavec-Škerget, Andreja Zagorac, Nadja Kokalj-Vokač
Publikováno v:
Acta Medico-Biotechnica. 4:51-60
Purpose: About 10-15% of all pregnancies terminate as spontaneous miscarriages. In the first trimester, ≈50% of spontaneous miscarriages are the result of chromosomal aberrations, mostly chromosomal aneuploidies. Cytogenetic analyses are used to co
Publikováno v:
Acta Medico-Biotechnica. 3:35-40
Purpose: To evaluate the diagnostic accuracy of the UroVysion FISH test for detecting transitional cell bladder cancer on a mixed sample of urological patients. Methods: Urine samples were collected from patients before cystoscopy. In the case of tum
Publikováno v:
Zdravniški Vestnik, Vol 72, Iss 6 (2003)
Background. Cryptic subtelomeric chromosome anomalies have been recognised as a significant cause of idiopathic mental retardation (IMR) and/or dysmorphology. This study presents an innovative simmultane fluorescence in situ hybridisation (FISH) tech
Externí odkaz:
https://doaj.org/article/ee28d5418841488bbeb951128a50f73f
Publikováno v:
Cancer Genetics and Cytogenetics. 195:19-22
TERC gene amplification was investigated as a possible diagnostic marker for use in routine cytological screening to improve the accuracy of conventional screening procedures in detection of cervical preneoplastic lesions. Cervical smears were screen
Autor:
Faris Mujezinović, Alenka Erjavec Škerget, Nadja Kokalj Vokac, Andreja Zagorac, Špela Stangler Herodež, Boris Zagradišnik
Publikováno v:
Genetic testing and molecular biomarkers. 17(9)
Quantitative-fluorescence polymerase chain reaction (QF-PCR) was used to detect common fetal aneuploidies in pregnancies with increased (maternal age) or high risk (increased nuchal translucency, abnormal fetal ultrasonography, positive biochemical h
Autor:
Mario Poljak, Andreja Zagorac, Darja Arko, Tatjana Kodrič, Alenka Erjavec-Škerget, Iztok Takač, Nadja Kokalj-Vokac
Publikováno v:
The Journal of international medical research. 37(5)
This study was designed to investigate whether a correlation exists between amplification of the human telomerase gene (human telomerase RNA component [ TERC]) and high-risk human papillomavirus (HR-HPV) infection in 101 women with cervical intra-epi
Autor:
Alenka Erjavec-Škerget, Špela Stangler-Herodež, Andreja Zagorac, Boris Zagradišnik, Nadja Kokalj-Vokač
Publikováno v:
Croatian Medical Journal
Volume 47
Issue 6
Volume 47
Issue 6
Aim To identify cryptic subtelomeric rearrangement, a possible cause of idiopathic mental retardation by means of multiprobe telomere fluorescent in situ hybridization (T-FISH). Methods Hundred patients (median age 3.0 years) with mental retardation