Wyniki wyszukiwania

1

Identification of minisatellite DNA markers for quantitative traits loci in geese

100%

Zawadzka M., Jaszczak K., Rabsztyn A.

Animal Science Papers and Reports

|

2001

|

tom 19

|

nr 1

2

Towards a genetic map of beet [Beta vulgaris L.]

100%

Jagosz B., Grzebelus D., Scholten O., Michalik B., Lange W.

Folia Horticulturae

|

1999

|

tom 11

|

nr 2

3

Inheritance of some omega-gliadin protein subunits in spelt wheat and their linkage with the red glume coding RG-1 locus

80%

Waga J.

Plant Breeding and Seed Science

|

2002

|

tom 46

|

nr 2

4

Artykuł dostępny w postaci pełnego tekstu - kliknij by otworzyć plik

Is the recently discovered EDA gene associated with anhidrotic ectodermal dysplasia?

80%

Kobielak K., Kobielak A., Trzeciak W. H.

Journal of Applied Genetics

|

1997

|

tom 38

|

nr 3

The evidence from literature strongly suggests that Christ-Siemens-Touraine (CST) syndrome is associated with mutations of the newly discovered EDA gene. The gene is situated on the long arm of the X chromosome (Xq12.2-q13.1) and contains two exons separated by a 200 kbp intron. The 5’-untranslated region and most of the coding sequence are localized in exon 1, while three C-terminal amino acids are encoded by exon 2. The coding sequence was interrupted by translocations in three affected females: t(X;l), t(X;12), t(X;9), and submicroscopic deletions of the EDA gene were found in five males with CST syndrome, and point mutations were discovered in exon 1 in nine other patients. Northern blot analysis and in situ hybridization studies revealed that the EDA gene was expressed in the foetus, and postnatally in a specific type of skin cell and that the expression was limited to cells of ectodermal origin. A predicted protein product of the EDA gene contains 135 to 140 amino acids, organized in three distinct domains and may belong to class II transmembrane receptors.

5

Usefulness of microsatellite markers in identification of family members carrying a mutation of the beta-myosin heavy chain gene in families with hypertrophic cardiomyopathy

80%

Smolik S., Domal-Kwiatkowska D., Mazurek U., Moric E., Nowalany-Kozielska E., Glanowska G., Kozakiewicz K., Wodniecki J., Tendera M., Wilczok T.

Journal of Applied Genetics

|

2000

|

tom 41

|

nr 3

Ograniczanie wyników

2 Journal of Applied Genetics

1 Animal Science Papers and Reports

1 Folia Horticulturae

1 Plant Breeding and Seed Science

1 Domal-Kwiatkowska D.

1 Glanowska G.

1 Grzebelus D.

1 Jagosz B.

1 Jaszczak K.

1 Kobielak A.

1 Kobielak K.

1 Kozakiewicz K.

1 Lange W.

1 Mazurek U.

1 Michalik B.

1 Moric E.

1 Nowalany-Kozielska E.

1 Rabsztyn A.

1 Scholten O.

1 Smolik S.

1 Tendera M.

1 Trzeciak W. H.

1 Waga J.

1 Wilczok T.

1 Wodniecki J.

1 Zawadzka M.

1 2002

1 2001

1 2000

1 1999

1 1997

Identification of minisatellite DNA markers for quantitative traits loci in geese

Towards a genetic map of beet [Beta vulgaris L.]

Inheritance of some omega-gliadin protein subunits in spelt wheat and their linkage with the red glume coding RG-1 locus

Is the recently discovered EDA gene associated with anhidrotic ectodermal dysplasia?

Usefulness of microsatellite markers in identification of family members carrying a mutation of the beta-myosin heavy chain gene in families with hypertrophic cardiomyopathy