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001-es BibID:BIBFORM039858
Első szerző:Mokánszki Attila (molekuláris biológus Ph.D hallgató)
Cím:Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH) / Attila Mokánszki, Anikó Ujfalusi, Erzsébet Balogh, Andrea Sümegi, Péter Antal-Szalmás, Zsuzsa Kassai Bazsáné, Zsuzsanna Molnár, Attila Varga, Tamás Sápy, Attila Jakab, Éva Oláh
Dátum:2012
ISSN:1939-6368
Megjegyzések:Male carriers with balanced reciprocal translocations can produce a variable proportion of unbalanced gametes resulting in reproductive failures. The presence of a structural rearrangement may induce an interchromosomal effect. This is characterized by abnormal bivalents not involved in the reorganization thereby yielding non-disjunction, which would present as aneuploid spermatozoa for these chromosomes. In the present case report segregation analysis of the sperm and investigationof interchromosomal effect were carried out using cytogenetic and fluorescence in situ hybridization (FISH) analysis on blood lymphocytes. The karyotype of the patient was 46,XY,t(3;6)(q21;q23). During sperm segregation analysis a total of 2,002 sperms were evaluated, of which 46.8% showed normal/balanced (alternate segregation mode) and 53.2% of sperm showed an abnormal signal pattern. A significant difference in the frequency of the estimated number of chromosome anomalies was observed in the translocation carrier when compared to the normozoospermic group (P < 0.0001) and the oligozoospermicgroup (P < 0.0001). Meiotic segregation analysisof sperm together with aneuploidy assessment for X, Y, and 17chromosomes using FISH allows for the determination of areproductive prognosis in male balanced translocation carriersand can be used for appropriate genetic counseling.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
balanced reciprocal translocation
interchromosomal effect
meiotic segregation analysis
sperm FISH
egyetemen (Magyarországon) készült közlemény
Megjelenés:Systems Biology in Reproductive Medicine. - 58 : 3 (2012), p. 160-164. -
További szerzők:Ujfalusi Anikó (1968-) (gyermekorvos, laboratóriumi szakorvos) Balogh Erzsébet (1949-) (biológus, citogenetikus) Sümegi Andrea (1969-) (biológus) Antal-Szalmás Péter (1968-) (laboratóriumi szakorvos) Bazsáné Kassai Zsuzsa (1946-) (embriológus) Molnár Zsuzsanna (1980-) (szülész-nőgyógyász, labor szakorvosjelölt, urológus) Varga Attila (1949-) (urológus, andrológus) Sápy Tamás (1970-) (szülész-nőgyógyász) Jakab Attila (1964-) (szülész-nőgyógyász, endokrinológus) Oláh Éva (1943-2019) (gyermekgyógyász, klinikai genetikus)
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2.

001-es BibID:BIBFORM039857
Első szerző:Mokánszki Attila (molekuláris biológus Ph.D hallgató)
Cím:Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients / Attila Mokánszki, Zsuzsanna Molnár, Anikó Ujfalusi, Erzsébet Balogh, Zsuzsa Kassai Bazsáné, Attila Varga, Attila Jakab, Éva Oláh
Dátum:2012
ISSN:1472-6483
Megjegyzések:Infertile men with low sperm concentration and/or less motile spermatozoa have an increased risk of producing aneuploid spermatozoa. Selecting spermatozoa by hyaluronic acid (HA) binding may reduce genetic risks such as chromosomal rearrangements and numerical aberrations. Fluorescence in-situ hybridization (FISH) has been used to evaluate the presence of aneuploidies. This study examined spermatozoa of 10 oligozoospermic, 9 asthenozoospermic, 9 oligoasthenozoospermic and 17 normozoospermic men by HA binding and FISH. Mean percentage of HA-bound spermatozoa in the normozoospermic group was 81%, which was significantly higher than in the oligozoospermic (P<0.001), asthenozoospermic (P<0.001) and oligoasthenozoospermic (P<0.001) groups. Disomy of sex chromosomes (P=0.014) and chromosome 17 (P=0.0019), diploidy (P=0.03) and estimated numerical chromosome aberrations (P=0.004) were significantly higher in the oligoasthenozoospermic group compared with the other groups. There were statistically significant relationships (P<0.001) between sperm concentration and HA binding (r=0.658), between sperm concentration and estimated numerical chromosome aberrations (r=-0.668) and between HA binding and estimated numerical chromosome aberrations (r=-0.682). HA binding and aneuploidy studies of spermatozoa in individual cases allow prediction of reproductive prognosis and provision of appropriate genetic counselling. Infertile men with normal karyotypes and low sperm concentrations and/or less motile spermatozoa have significantly increased risks of producing aneuploid (diminished mature) spermatozoa. Selecting spermatozoa by hyaluronic acid (HA) binding, based on a binding between sperm receptors for zona pellucida and HA, may reduce the potential genetic risks such as chromosomal rearrangements and numerical aberrations. In the present study we examined sperm samples of 45 men with different sperm parameters by HA-binding assay and fluorescence in-situ hybridization (FISH). Mean percentage of HA-bound spermatozoa in the normozoospermic group was significantly higher than the oligozoospermic, the asthenozoospermic and the oligoasthenozoospermic groups. Using FISH, disomy of sex chromosomes and chromosome 17, diploidy and estimated numerical chromosome aberration frequencies were significantly higher in the oligoasthenozoospermic group compared with the three other groups. A significant positive correlation was found between the sperm concentration and the HA-binding capacity, and significant negative correlations between the sperm concentration and the estimated numerical chromosomes aberrations as well as between the HA-binding ability and the estimated numerical chromosome aberrations were identified. We conclude that HA-binding assay and sperm aneuploidy study using FISH may help to predict the reproductive ability of selected infertile male patients and to provide appropriate genetic counselling.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
lissencephaly
subcortical band heterotopia
LIS1 (PAFAH1B1)
DCX
TUBA1A
pachygyria
agyria
egyetemen (Magyarországon) készült közlemény
Megjelenés:Reproductive Biomedicine Online. - 25 : 6 (2012), p. 620-626. -
További szerzők:Molnár Zsuzsanna (1980-) (szülész-nőgyógyász, labor szakorvosjelölt, urológus) Ujfalusi Anikó (1968-) (gyermekorvos, laboratóriumi szakorvos) Balogh Erzsébet (1949-) (biológus, citogenetikus) Bazsáné Kassai Zsuzsa (1946-) (embriológus) Varga Attila (1949-) (urológus, andrológus) Jakab Attila (1964-) (szülész-nőgyógyász, endokrinológus) Oláh Éva (1943-2019) (gyermekgyógyász, klinikai genetikus)
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DOI
Intézményi repozitóriumban (DEA) tárolt változat
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