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To the memory of professor Teresa Hulewicz [1916 - 1994]

100%

Jassem M.

Journal of Applied Genetics

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1995

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tom 36

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nr 2

2

Indentification of three different chromosomal additions by chromosome painting using fluorescence in situ hybridization [FISH] technique

88%

Bocian E., Stankiewicz P., Stanczak H., Obersztyn E., Mazurczak T., Mazurczak T.

Journal of Applied Genetics

|

1996

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tom 37

|

nr 2

Fluorescence in situ hybridization (FISH) is a very useful method for assessing chromosome rearrangements. When neither banding pattern nor clinical symptoms are sufficient to determine the origin of additional chromosomal fragment, FISH with multiple chromosome-specific libraries (chromosome painting), allows to solve this diagnostic problem rapidly. Three chromosomal additions, 7q+, 13p+ and 22q+, found in routine cytogenetic studies performed in children with phenotypic abnormalities were analysed using FISH. This technique documented the origin of the extra material to be derived from chromosome 16[der(7)t(7; 16)(q36.3;p 13.11)], 18[der(13)t(13; 18)(p12;q 12.2)] and 22[dup(22)(q11.2q13.1)], respectively. In two cases the abnormality arose de novo, while in the third case the product of translocation t(13;18) was maternal by origin. It was present in 30% of mother's lymphocytes, and in 70% of them a balanced Robertsonian translocation t(13q;15q) was found. In the presented cases the chromosome analysis with both traditional banding and chromosome painting techniques, allowed to establish final clinical diagnosis.

3

Androgenetic response of Polish wheat varieties

88%

Czaplicki A.

Polish Journal of Natural Sciences. Supplement

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2003

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tom 01

4

Cytogenetics, embryology and fertility of red clover [Trifolium pratense L.] with short flowers and anthocyanin spots on the leaves

88%

Kazimierski T., Kazimierska E. M.

Journal of Applied Genetics

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1995

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tom 36

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nr 4

Anthocyanin spot on the leaves of red clover is inherited independently of light spot and uniform leaf colour. The gene determining anthocyanin spot is probably localized on the other chromosome than the gene determining light spot on the leaves. A short flower tube is also determined by a single recessive gene of a pleiotropic action. It simultaneously causes reduction of pistil style, thickening of the endothecium layer in anthers - entails their indehiscence, pollen grain-agglutination and often deformation, no division of part of pollen grains into a vegetative and generative cells as well as germination of single grains in pollen sacks. The changes in the structure of endothecium and pollen grains cause almost complete male and female infertility of plants with short flower tubes.

5

Comparison of GTG-banded karyotypes and microsatellite sequences in some species of the Bovidae and Cervidae families

75%

Kozubska-Sobocinska A., Zabek T., Slota E., Kaczor U.

Journal of Animal and Feed Sciences

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2007

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tom 16

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nr 4

565-576

6

FISH mapping in cattle (Bos taurus L.) is not yet out of fashion

75%

De Lorenzi L., Molteni L., Parma P.

Journal of Applied Genetics

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2010

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tom 51

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nr 4

Physical mapping of genes by fluorescence in situ hybridization (FISH) seems to be out of fashion in species whose assembled genome sequences are available. However, in this work we evidence the existence of errors in gene location in the Btau_4.0 assembly. We show that DFNA5 and CHCHD6 genes are located on BTA4 and BTA22, respectively, instead of BTA10 and BTA3, as displayed by Btau_4.0. This report emphasizes the need to verify the data on physical localization of genes in the cattle genome (at least by taking into account comparative data reported in available papers) and the need to improve the cattle genome assembly. Our results indicate that FISH mapping in cattle is still useful.

7

Acquired pericentric inversion of chromosome 9 in acute myeloid leukemia

75%

Udayakumar A. M., Pathare A. V., Dennison D., Raeburn J. A.

Journal of Applied Genetics

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2009

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tom 50

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nr 1

73-76

Pericentric inversion of chromosome 9 involving the qh region is relatively common as a constitutional genetic aberration without any apparent phenotypic consequences. However, it has not been established as an acquired abnormality in cancer. Among the three patients reported so far in the literature with acquired inv(9), only one had acute myeloid leukemia (AML). Here we describe an unique case where both chromosomes 9 presented with an acquired pericentric inversion with breakpoints at 9p 13 and 9q 12 respectively, in a AML patient with aberrant CD7 and CD9 positivity. Additionally, one der(9) also showed short arm deletion at 9p21 to the centromeric region and including the p 16 gene. The constitutional karyotype was normal. This is probably the first report describing an acquired inv(9) involving both chromosomes 9 in AML. The possible significance of this inversion is discussed.

8

Cytogenetic study of embryos from ducks maintained in conservative flocks

75%

Jaszczak K., Ksiazkiewicz J., Parada R., Sacharczuk M.

Journal of Animal and Feed Sciences

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2005

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tom 14

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nr 3

571-575

9

First description of supernumerary chromosomes in Ictalurus punctatus Rafinesque 1818 reveals active ribosomal genes in the B complement

75%

Prado F. D., Daniel S. N., Penitente M., Hashimoto D. T., Foresti F., Porto-Foresti F.

Folia Biologica

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2016

|

tom 64

|

nr 4

10

Infertility and marker chromosomes: Application of molecular cytogenetic techniques in a case of inv dupp.89-91,fig.,ref.

75%

Vulcani-Freitas T. M., Gil-da-Silva-Lopes V. L., Varella-Garcia M., Maciel-Guerra A. T.

Journal of Applied Genetics

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2006

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tom 47

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nr 1

We report on a phenotypically normal man with infertility, whose 47,XY,+mar karyotype was studied by spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH) using a chromosome-15-specific probe (LSI SNRPN). By these techniques, the marker chromosome was identified as a small inv dup (15). Possible causes for male infertility in this case are discussed.

11

Chromosome study of peled [Coregonus peled, Salmoniformes]

75%

Kirtiklis L., Jankun M.

Folia Biologica

|

2004

|

tom 52

|

nr 3-4

12

Cytogenetic status of barley plants regenerated from anther culture

75%

Szarejko I., Janusz A., Nabialkowska D., Trojanowska A.

Prace Naukowe Uniwersytetu Śląskiego w Katowicach

|

1998

|

tom 1696

13

Chromosome preparation from human bone marrow - technique modified for immediate clinical investigation

75%

Sett R. N.

Folia Biologica

|

1992

|

tom 40

|

nr 1-2

14

Comparative cytogenetic study of Poecilimon brunneri Frivaldsky and P.zwicki Ramme [Phaneropteridae: Orthoptera]

75%

Warchalowska-Sliwa E., Michailova P. V., Peshev G.

Folia Biologica

|

1992

|

tom 40

|

nr 1-2

15

Distribution and heterogeneity of heterochromatin in the European huchen (Hucho hucho Linnaeus, 1758) (Salmonidae)

63%

Kucinski M., Ocalewicz K., Fopp-Bayat D., Liszewski T., Furgala-Selezniow G., Jankun M.

Folia Biologica

|

2014

|

tom 62

|

nr 2

16

The cytogenetics and molecular characteristics of a translocated chromosome 1AS.1AL-1DL with a Glu-D1 locus in durum wheat

63%

Blanco A., Cenci A., Simeone R., Gadaleta A., Pignone D., Galasso I.

Cellular and Molecular Biology Letters

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2002

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tom 07

|

nr 2A

Wheat quality depends directly on the grain protein content and protein composition. High and low molecular weight glutenin subunits play an important role in determining the visco-elastic properties of gluten. In an attempt to improve the breadmaking quality of hexaploid triticale, a fragment of wheat chromosome 1D, containing the Glu-D1 allele encoding the 5+10 subunits, was translocated to the long arm of chromosome 1A by Lukaszewski and Curtis [1], The 1A.1D translocation chromosome was transferred to tetraploid wheat [2], making the Glu-D1 locus available for the improvement of durum wheat. The goal of this study was to evaluate using cytogenetics and molecular approaches the amount of chromatin introgressed in durum wheat. Fluorescence in situ hybridization with total genomic DNA (GISH) of Aegilops squarrosa L. indicated that the translocated chromosome 1A.1D had a terminal 1DL segment of about 35-40% of the recombinant arm length. Several pairs of microsatellite primers from chromosome 1A and 1D were used to genetically characterize the recombinant chromosome. The mapping data indicated that a 1AL segment, at least 150 cM long, was substituted by a 1DL segment with a minimal length of 72 cM, and that the translocation breakpoint was near the 1A centromeric region. The genetic and physical data highlight a substantial discrepancy between the recombinational and physical map distances. We are using a targeted strategy via the Ph pairing manipulation system to generate smali intercalary 1D chromosome segments in a durum wheat background.

17

Comparison of the G-banded karyotype of the fallow deer (Dama dama) and sheep (Ovis aries)

63%

Kozubska-Sobocinska A., Slota E., Pakusiewicz M.

Annals of Animal Science

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2006

|

tom 06

|

nr 2

18

Wykorzystanie oceny prawidlowosci kariotypu w hodowli zwierzat gospodarskich

63%

Slota E., Danielak B., Rejduch B., Kozbuska-Sobocinska A., Sysa P. S.

Biuletyn Informacyjny. Instytut Zootechniki

|

1993

|

tom 31

|

nr 5-6

21-30

19

Y chromosome polymorphism in some species of Bovidae

63%

Kozubska-Sobocinska A., Slota E.

Annals of Animal Science

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2002

|

tom 02

|

nr 1

20

Professor Romana Czapik - biographical note

63%

Jankun A.

Acta Biologica Cracoviensia. Series Botanica

|

1999

|

tom 41

Ograniczanie wyników

To the memory of professor Teresa Hulewicz [1916 - 1994]

Indentification of three different chromosomal additions by chromosome painting using fluorescence in situ hybridization [FISH] technique

Androgenetic response of Polish wheat varieties

Cytogenetics, embryology and fertility of red clover [Trifolium pratense L.] with short flowers and anthocyanin spots on the leaves

Comparison of GTG-banded karyotypes and microsatellite sequences in some species of the Bovidae and Cervidae families

FISH mapping in cattle (Bos taurus L.) is not yet out of fashion

Acquired pericentric inversion of chromosome 9 in acute myeloid leukemia