Wyniki wyszukiwania

1

Molecular cloning and sequencing og the cDNA encoding plant 22 kDa nuclease

100%

Szmidzinski R., Wilczynski G., Szopa J.

Acta Biochimica Polonica

|

1994

|

tom 41

|

nr 2

2

Zawartosc jadrowego DNA w komorkach gesi domowej Anser anser

86%

Andraszek K., Smalec E.

Roczniki Naukowe Polskiego Towarzystwa Zootechnicznego

|

2007

|

tom 03

|

nr 1

9-17

3

Sekwencjonowanie RNA - wszechstronna metoda poznania transkryptomu

86%

Domka A., Domka B., Kornas A.

Postępy Biologii Komórki

|

2014

|

tom 41

|

nr 4

4

Przeszukiwanie bazy danych EST w celu zidentyfikowania pelnej sekwencji cDNA genu kodujacego akwaporyne Pharbitis nil Choisy [PnPIP1]

86%

Dabrowska G., Mordaka P. M.

Biotechnologia

|

2008

|

nr 2

190-198

5

Infekcyjne klony cDNA roslinnych wirusow

86%

Sadowy E., Zagorski W., Hulanicka D.

Biotechnologia

|

1996

|

nr 3

60-68

6

Potato plants over- and underexpressing 14-3-3 protein isoforms

86%

Wilczynski G., Kulma A., Szopa J.

Cellular and Molecular Biology Letters

|

1997

|

tom 02

|

nr 2

7

Towards an understanding of the functional significance for N-terminal domain divergence in human AMP deaminase isoform

86%

Sabina R. L., Mahnke-Zizelman D. K.

Cellular and Molecular Biology Letters

|

1999

|

tom 04

|

nr 3

8

Isolation and classification of a family of cyclin gene homologues in Lupinus luteus

86%

Deckert J., Jelenska J., Zaborowska Z., Legocki A. B.

Acta Biochimica Polonica

|

1997

|

tom 44

|

nr 1

The lupine (Lupinus luteus cv. Ventus) cDNA clones encoding homologues of cyclin (CycBlfi, CycBl;3, CycBl;4) have been Isolated from cDNA library prepared from roots inoculated with Bradyrhizobium lupint. Comparison of the deduced amino-acid sequences of CycBlg, CycBl;3, CycBl;4 and previously described CycBl;l (Deckert et al 1996, Biochimie 78, 90-94) showed that they share 46-65% of identical amino acids. The presence of conserved residues (Renaudin et al., in The Plant Cell Cycle, in the press; Renaudin et al.. Plant Mol. Biol., in the press) along with phylogenetic analysis of known plant cyclins revealed that the four lupine sequences belong to subgroup I of B-like mitotic cyclins.

9

The repression of six 14-3-3 isoforms resulting in the activation of NR and SPS and an increase in the antioxidant properties of transgenic potato plants

86%

Zuk M., Szopa J.

Cellular and Molecular Biology Letters

|

2002

|

tom 07

|

nr Suppl.

10

Molecular cloning and sequencing of the cDNA encoding plant nuclear matrix endonuclease

86%

Markiwicz E., Rzepecki R., Szopa J.

Acta Biochimica Polonica

|

1994

|

tom 41

|

nr 2

11

Cytosolic purine 5'-nucleotidase from chicken heart: an isozyme of the liver enzyme as evidenced by northern blot analysis

86%

Oka J.

Cellular and Molecular Biology Letters

|

1999

|

tom 04

|

nr 3

12

The 3' untranslated region of mRNAs from the ciliate Nyctotherus ovalis

86%

Destables E., Thomas N. A., Boxma B., Van Alen T. A., Van der Staay G. W. M., Hackstein J. H. P., McEwan N. R.

Acta Protozoologica

|

2005

|

tom 44

|

nr 3

13

Isolation and characterization of a serine-threonine protein kinase SOS2 gene from Brassica napus

86%

Wang J., Wu W., Zuo K., Fei J., Sun X., Lin J., Li X., Tang K.

Cellular and Molecular Biology Letters

|

2004

|

tom 09

|

nr 3

A full-length cDNA of a new serine/threonine (Ser/Thr) protein kinase gene, designated as BnSOS2 (GenBank Acc. No.AY310413), was cloned from Brassica napus by rapid amplification of cDNA ends (RACE). The fulllength cDNA of BnSOS2 was 1779 bp and contained a 1539-bp open reading frame encoding a protein of 512 amino acids. Homology analysis shows that BnSOS2 strongly resembles other Ser/Thr protein kinase genes, and that its putative protein belongs to a typical Ser/Thr kinase family. Northern blot analysis reveals that BnSOS2 is salt-inducible. Our results indicate that BnSOS2 is a new member of the plant SOS2 gene family, which may play an important role in salt tolerance of plants.

14

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Identyfikacja cDNA genu RSH [RelA-SpoT homolog] zaangazowanego w odpowiedz Pharbitis nil na warunki stresowe

81%

Dabrowska G., Prusinska J., Goc A.

Zeszyty Problemowe Postępów Nauk Rolniczych

|

2006

|

tom 509

333-341

Stres środowiskowy jest z jednym z głównych czynników limitujących wzrost i rozwój roślin. Przeszukiwanie biblioteki cDNA Pharbitis nil z liścieni roślin zaindukowanych do kwitnienia sondą SOD3.1 kodującą manganową dysmutazę ponadtlenkową pszenicy, umożliwiło zidentyfikowanie sekwencji długości 798 pz. Sekwencja ta wykazuje najwyższą homologię do roślinnych genów RSH, homologicznych do bakteryjnych RelA i SpoT. Białka kodowane przez te geny uczestniczą w odpowiedzi ścisłej - wysoce konserwowanym mechanizmie odpowiedzi na stres.

15

The alterations in SATB1 and nuclear F-actin expression affect apoptotic response of the MCF-7 cells to geldanamycin

72%

Grzanka D., Izdebska M., Klimaszewska-Wisniewska A., Gagat M.

Folia Histochemica et Cytobiologica

|

2015

|

tom 53

|

nr 1

16

Charakterystyka roslin ogorka uzyskanych po transformacji cDNA genu taumatyny II

72%

Szwacka M., Morawski M., Malepszy S.

Zeszyty Naukowe Akademii Rolniczej w Krakowie. Sesja Naukowa

|

1997

|

tom 50

517-520

17

Molecular cloning and preliminary expression analysis of complete cDNA homologue LOX2 gene in Lupinus luteus

72%

Wilmowicz E., Kucko A., Frankowski K., Kesy J., Marciniak K., Glazinska P., Banach M., Wojciechowski W., Kopcewicz J., Tretyn A.

BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology

|

2013

|

tom 94

|

nr 3

18

Sklonowane cDNA genow pPAG [porcine Pregnancy-Associated Glycoprotein] jako uzyteczne matryce wykorzystywane do proteomiki i genomiki diagnostycznej

72%

Panasiewicz G., Szafranska B.

Biotechnologia

|

2005

|

nr 1

47-60

19

Cloning of complete Pharbitis nil water channel cDNA (PnPIP1). PnPIP1 expression in seedlings under darkness conditions

72%

Dabrowska G., Mordaka P., Prusinska J., Srawski K., Goc A.

Acta Physiologiae Plantarum

|

2007

|

tom 29

|

nr 1 Suppl.

20

Polymerase chain reaction: amplification and sequencing of the VP1 gene of foot-and-mouth disease virus type A

72%

Paprocka G., Plucienniczak A.

Bulletin of the Veterinary Institute in Puławy

|

1996

|

tom 40

|

nr 2

The polymerase chain reaction method (PCR) has been applied to the detection of FMD viral RNA in samples taken from the calf during the clinical stage of FMD. Total RNA was extracted with a guanidinum thiocyanate-phenol-chloroform method and reverse transcribed using AMV-reverse transcriptase. cDNA was used as a template for the amplification by PCR of the 672 bp of the VP1 coding sequence. The amplified fragment of cDNA was cloned in the pBS(+) phagemid-containing sites recognized by Smal endonuclease and expressed in E. coli strain MV1193. The first DNA strand was sequenced and concurrently an amino acid sequence was established. Comparison between VP1 amino acid sequence of FMDV types A and earlier described type O was performed.

Ograniczanie wyników

Molecular cloning and sequencing og the cDNA encoding plant 22 kDa nuclease

Zawartosc jadrowego DNA w komorkach gesi domowej Anser anser

Sekwencjonowanie RNA - wszechstronna metoda poznania transkryptomu

Przeszukiwanie bazy danych EST w celu zidentyfikowania pelnej sekwencji cDNA genu kodujacego akwaporyne Pharbitis nil Choisy [PnPIP1]

Infekcyjne klony cDNA roslinnych wirusow

Potato plants over- and underexpressing 14-3-3 protein isoforms

Towards an understanding of the functional significance for N-terminal domain divergence in human AMP deaminase isoform

Isolation and classification of a family of cyclin gene homologues in Lupinus luteus