Autor: Kamiński, S. - Katalog OPAC zbiorów

Skocz do pozycji: 1.

Tytuł:: Novel method for identification of the lethal mutation in bovine APAF1 geneand its preliminary prevalence in Polish Holstein-Friesian bulls
Autorzy:: Kamiński, S.
Powiązania:: https://bibliotekanauki.pl/articles/2087363.pdf
Data publikacji:: 2020
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: Holstein bull
lethal genetic defect
carrier
APAF1 gene
Źródło:: Polish Journal of Veterinary Sciences; 2020, 23, 1; 157-160
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 2.

Tytuł:: Missense mutation in SDE2 gene – new lethal defect transmitted into Polish Holstein-Friesian cattle
Autorzy:: Kamiński, S.
Powiązania:: https://bibliotekanauki.pl/articles/2087487.pdf
Data publikacji:: 2019
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: Holstein bull
lethal genetic defect
carrier
SDE2 gene
Źródło:: Polish Journal of Veterinary Sciences; 2019, 3; 627-630
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 3.

Tytuł:: Bovine kappa-casein [CASK] gene - molecular nature and application in dairy cattle breeding
Autorzy:: Kaminski, S
Powiązania:: https://bibliotekanauki.pl/articles/2047276.pdf
Data publikacji:: 1996
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: bovine kappa-casein
quantitative trait locus
polymorphism
gene frequency
milk protein content
genotype
cattle breeding
dairy cattle
Opis:: The bovine kappa-casein (CASK) gene is considered a potential marker for quantitative trait loci (QTL) in dairy cattle. A large amount of research has been performed to explore the nature and variation of the CASK gene and its possible applications in cattle breeding. The purpose of this review is to sum up the knowledge of all known aspects of the CASK gene: molecular structure and function, polymorphism and allele freqeuncy, methods of genotyping and possibilities of the use of CASK polymorphism in dairy cattle breeding.
Źródło:: Journal of Applied Genetics; 1996, 37, 2; 179-196
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 4.

Tytuł:: Dde I RFLP at the 5 region of bovine kappa-casein gene
Autorzy:: Kaminski, S
Powiązania:: https://bibliotekanauki.pl/articles/2047278.pdf
Data publikacji:: 1996
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: gene region
bovine kappa-casein
polymorphism
milk property
dairy cattle
Opis:: The bovine kappa-casein (CASK) gene is known as a potential quantitative trait locus in dairy cattle breeding. However, the molecular basis of the effect of the CASK allele B on different milk properties remains unclear. In this report, a 214 bp fragment of the 5' untranslated region of the CASK gene containing 5 potential consensus sequenses for different transcription factors was PCR-amplified to find RFLPs. A Dde I RFLP was identified. In a population of 112 Bos taurus (86 cows and 26 bulls of Polish Black and White crossbred Holstein-Friesian) and 7 Bison bonasus individuals, 7 had no recognition sites for Dde I, 23 were heterozygous and 89 were cut completely into two fragments.
Źródło:: Journal of Applied Genetics; 1996, 37, 2; 173-178
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 5.

Tytuł:: Associations between bovine beta-lactoglobulin polymorphism within coding and regulatory sequences and milk performance traits
Autorzy:: Kaminski, S
Zabolewicz, T.
Powiązania:: https://bibliotekanauki.pl/articles/2043147.pdf
Data publikacji:: 2000
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: chromosome
polymorphism
promoter
haplotype
beta-lactoglobulin gene
mutation
cattle breeding
amino acid
milk
dairy cattle
protein content
Źródło:: Journal of Applied Genetics; 2000, 41, 2; 91-99
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 6.

Tytuł:: SSCP polymorphism within 5 region of bovine lactoglobulin [LGB] gene
Autorzy:: Kaminski, S
Zabolewicz, T.
Powiązania:: https://bibliotekanauki.pl/articles/2044462.pdf
Data publikacji:: 1998
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: lactoglobulin gene
polymorphism
SSCP method
cattle
gene transcription
electrophoresis
hormonal receptor
mutation
beta-lactoglobulin
milk
Opis:: In the paper the detection of the SSCP polymorphism within the 5’ fragment of bovine beta-lactoglobulin (LGB) gene is described. The 5’ fragment of LGB gene (209 bp) was PCR-amplified and then subjected to electrophoresis allowing the detection of SSCP polymorphism. Among 124 animals (50 cows and 74 bulls) six SSCP patterns were identified and named Rl, R2, R3, R4, R5 and R6, which occured with the frequency of 0.32, 0.51, 0.09, 0.06, 0.01 and 0.01, respectively. The PCR-SSCP method is simple, fast, and relatively inexpensive. The SSCP polymorphism reported in the paper may be useful in looking for the associations between different SSCP patterns and LGB gene expression and milk properties.
Źródło:: Journal of Applied Genetics; 1998, 39, 1; 97-102
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 7.

Tytuł:: Detection of bovine leucocyte adhesion deficiency [BLAD] carriers using a new PCR test
Autorzy:: Kaminski, S
Czarnik, U
Powiązania:: https://bibliotekanauki.pl/articles/2046599.pdf
Data publikacji:: 1997
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: cattle
bovine leucocyte adhesion deficiency
polymerase chain reaction
bacterial infection
Opis:: In this report we demonstrate a simple, effective and reliable diagnostic test of BLAD carrier detection based on specific PCR amplification of a 367 bp CD18 gene fragment and RFLP analysis using Taq I restriction enzyme. In a non-random population of 220 animals we found 48 BLAD carriers. Within the amplified PCR fragment an unknown intron sequence of 159 bp was identified.
Źródło:: Journal of Applied Genetics; 1997, 38, 1; 51-55
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 8.

Tytuł:: Genotyping of bovine beta-lactoglobulin [LGB] by PCR-SSCP technique
Autorzy:: Kaminski, S
Zabolewicz, T
Powiązania:: https://bibliotekanauki.pl/articles/2046615.pdf
Data publikacji:: 1997
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: AB genotype
SSCP method
cattle
genotype
AA genotype
BB genotype
beta-lactoglobulin
polymerase chain reaction
allele
identification
Opis:: A new method facilitating the identification of the two most common alleles (A and B) of the bovine beta-lacoglobulin (LGB) gene is described. The method is based on two steps: PCR amplification of 240 bp fragment of LGB gene followed by the single stranded conformation polymorphism (SSCP) detection. AA, AB and BB genotypes of LGB were identified with this technique. The PCR-SSCP is simple, accurate and relatively inexpensive. Additionally, this method has a potential to detect new variants within the amplified gene fragment.
Źródło:: Journal of Applied Genetics; 1997, 38, 4; 471-476
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 9.

Tytuł:: Detection of Brachyspina carriers within Polish Holstein-Friesian bulls
Autorzy:: Rusc, A.
Kaminski, S.
Powiązania:: https://bibliotekanauki.pl/articles/31551.pdf
Data publikacji:: 2015
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:: The aim of this paper was to verify the hypothesis whether carriers of genetic defect Brachyspina occur in the Polish Holstein-Friesian Cattle. PCR method was used to screen 78 Polish Hol-stein-Friesian bulls. Eight bulls were identified as heterozygotes for 3,3 kb deletion in the FANCI gene - the mutation causing Brachyspina defect. All carriers were sons of 3 sires: Cleitus Jabot, Sandy-Valley Bolton ET and Coyne-Farms Dorcy ET which were descendants of the US sire Sweet Haven Tradition (HOUSAM 1682485). Systematic screening of young bulls having in the pedigree Barchyspina carrier is necessary to prevent spreading of the recessive mutation in the dairy cattle population in Poland.
Źródło:: Polish Journal of Veterinary Sciences; 2015, 18, 2
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 10.

Tytuł:: Cholesterol Deficiency - new genetic defect transmitted to Polish Holstein-Friesian cattle
Autorzy:: Kaminski, S.
Rusc, A.
Powiązania:: https://bibliotekanauki.pl/articles/30953.pdf
Data publikacji:: 2016
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:: The aim of the study was to find out whether carriers of new genetic defect Cholesterol Deficiency (CD) occur in the population of Polish Holstein-Friesian bulls. Twenty seven bulls were included in the analysis. Bulls were selected as having in the pedigree known carrier of CD (Maughlin Storm CANM000005457798). All bulls were diagnosed by the test described by Menzi et al. (2016) by using allele-specific PCR. Among 27 bulls, 9 new CD carriers were found. Our results show that causal mutation for CD is already transmitted to Polish Holstein-Friesian cattle. The results are sufficient ground to take practical action in order to avoid further spreading of mutation causing CD.
Źródło:: Polish Journal of Veterinary Sciences; 2016, 19, 4
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 11.

Tytuł:: Bovine leucocyte adhesion deficiency [BLAD] and its worldwide prevalence
Autorzy:: Pareek, C S
Kaminski, S
Powiązania:: https://bibliotekanauki.pl/articles/2047260.pdf
Data publikacji:: 1996
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: gene
prevalence
clinical diagnosis
diagnosis
Holstein breed
cattle
clinical finding
bovine leucocyte adhesion deficiency
animal disease
Opis:: Bovine leukocyte adhesion deficiency (BLAD) is a well characterised lethal autosomal recessive disease that occurs in Holstein cattle. The discovery of this genetic disorder in 1990 by KEHRLI et al. was serendipitous and occurred in conjunction with studies of new methods to prevent mastitis in periparturient dairy cows ( KEHRLI et al. 1992a). In this review article we are attempting to summarise the last 6-year research (1990-1995) covering major aspects of BLAD syndrome, its worldwide prevalence with emphasize on current and future development on BLAD research.
Źródło:: Journal of Applied Genetics; 1996, 37, 3; 299-311
1234-1983
Pojawia się w:: Journal of Applied Genetics
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 12.

Tytuł:: Association between SOX5 genotypes and semen quality in Polish Holstein-Friesian bulls
Autorzy:: Hering, D.M.
Kaminski, S.
Powiązania:: https://bibliotekanauki.pl/articles/32539.pdf
Data publikacji:: 2016
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:: The aim of this study was to evaluate the effect of C/T missense mutation (SOX5) gene on selected parameters of non-frozen semen in Polish Holstein – Friesian bulls. Three hundred and sixty eight bulls were genotyped by the PCR-Rsa I technique. Semen was collected and evaluated by standardized procedure used in an AI station. Significant associations were found between SOX5 genotypes and sperm concentrations (p=0.020) and sperm motility (p=0.014). Bulls with TT genotype had the lowest values of both traits. Our results demonstrate that C/T missense mutation within the SOX5 gene is involved in bull sperm quality.
Źródło:: Polish Journal of Veterinary Sciences; 2016, 19, 3
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 13.

Tytuł:: Single nucleotide polymorphism within arylsulfatase D gene (ARSD) is associated with selected kinematic parameters of sperm motility in Holstein-Friesian bulls
Autorzy:: Hering, D.
Lecewicz, M.
Kordan, W.
Kaminski, S.
Powiązania:: https://bibliotekanauki.pl/articles/30896.pdf
Data publikacji:: 2014
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:: The aim of the study was to find out whether the single nucleotide polymorphism (SNP) within arylsulfatase D (ARSD) gene is associated with kinematic parameters of sperm motility in Holstein- Friesian bulls. 367 Holstein-Friesian bulls kept in one AI center were included in the study. Point mutation C/T at position 139037255 on chromosome X (rs42207167) was identified by PCR-RFLP method (Pflm I). Significant associations were found between ARSD genotypes and CASA-derived sperm motility parameters: average TM (Total Motility), average VSL (Straight Velocity), average VCL (Curvilinear Velocity) and for fraction of sperms showing progressive motility (a) of sperms (VSLa, VCLa and BCFa -Beat Cross Frequency). Most significant differences were observed between alternative homozygotes (CC vs TT). Our results suggest new role of arylsulfatase D gene as being involved in sperm motility.
Źródło:: Polish Journal of Veterinary Sciences; 2014, 17, 3
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 14.

Tytuł:: Missense mutation within cystic fibrosis transmembrane conductance regulator (CFTR) gene is associated with selected parameters of the frozen-thawed spermin Holstein-Friesian bulls
Autorzy:: Kaminski, S.
Hering, D.M.
Kordan, W.
Lecewicz, M.
Powiązania:: https://bibliotekanauki.pl/articles/2087549.pdf
Data publikacji:: 2019
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: bull
sperm
polymorphism
CFTR gene
antioxidant enzyme activity
Źródło:: Polish Journal of Veterinary Sciences; 2019, 2; 221-225
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 15.

Tytuł:: Screening of Polish Holstein-Friesian bulls towards eradication of Complex Vertebral Malformation (CVM) carriers
Autorzy:: Rusc, A.
Hering, D.
Puckowska, P.
Barcewicz, M.
Kaminski, S.
Powiązania:: https://bibliotekanauki.pl/articles/32473.pdf
Data publikacji:: 2013
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:: The effectiveness of a program aimed at eradicating carriers of the recessive disorder Complex Vertebral Malformation (CVM) from the population of Holstein-Friesian bulls is reported. Among 1823 bulls, 1268 young and 555 proven bulls were examined. Three hundred and three bulls appeared to be CVM carriers (16.62%). The highest number of carriers occurred in the sons of a CVM sire, 55.51% and 61.90%, for proven and young bulls, respectively. This very high incidence of CVM carriers forced us to implement a strategy of screening young bulls offered by individual breeders to insemination centers. In effect, the number of CVM carriers dramatically dropped among proven bulls born in 2004 and disappeared in bulls born in 2006.
Źródło:: Polish Journal of Veterinary Sciences; 2013, 16, 3
1505-1773
Pojawia się w:: Polish Journal of Veterinary Sciences
Dostawca treści:: Biblioteka Nauki

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