Výsledky 581 – 590 z 961 (0,550 sekund)

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A default theory of default case.

CAHA, Pavel

Vydání: GLOW 46, Vienna, 12. 4. 2023, 2023.

non-decomposable cases (NOM, ACC, GEN) place no restrictions ... non-decomposable cases (NOM, ACC, GEN) place no restrictions ... Non-decomposable case (NOM, ACC, GEN) 17
https://is.muni.cz/publication/2274797/glow-caha.pdf

Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on ...

BURCKHARDT, Daniel, Liliia SERBINA, Igor MALENOVSKÝ, Dalva L. QUEIROZ, Desiree C. ALENE, Geonho CHO a Diana M. PERCY

Vydání: Zoological Journal of the Linnean Society, Oxford, Oxford University Press, 2024, 0024-4082.

ISSN: 0024-4082, UT ISI: 001100988400001

SMALL LETTER Y WITH ACUTE, gen. nov., Melanastera Serbina, MalenovskATIN SMALL ... WITH ACUTE, Queiroz and Burckhardt, gen. nov. and Woldaia stat. rev ... SMALL LETTER Y WITH ACUTE, gen. nov. and Paurocephala s.s
https://is.muni.cz/publication/2408398

Pedběžné výsledky výzkumu neogenních obratlovců z lokality Mokrá-lom.

IVANOV, Martin a Rudolf MUSIL

Název anglicky: Preliminary results of investigation of Neogene vertebrates from the Mokrá-Quarry site

Vydání: Acta Musei Moraviae, Scientiae geologicae, Brno, 2004, 1211-8796.

cf. paradoxus, Pelobates sp., Emydidae gen et sp. indet. (zřejmě Chrysemys sp.), Testudinidae gen et sp. indet. (zřejmě Testudo ... Lacerta sp. (malá forma), Boidae gen et sp. indet. (velká forma
https://is.muni.cz/publication/562707

Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I ...

FREIBERGER, Tomáš, Lenka KOLÁŘOVÁ, Pavel MEJSTŘÍK, Martina VYSKOČILOVÁ, Pavel KUKLÍNEK a Jiří LITZMAN

Vydání: Human Mutation, 2002, 1059-7794.

in the C1 inhibitor gene (C1NH) leading to ... of the C1 inhibitor gene is presented. Five novel mutations ... in the C1 inhibitor gene in five families with type
https://is.muni.cz/publication/484323

Different spectra of recurrent gene mutations in subsets of chronic lymphocytic leukemia harboring stereotyped B-cell receptors.

SUTTON, Lesley-Ann, Emma YOUNG, Panagiotis BALIAKAS, Anastasia HADZIDIMITRIOU, Theodoros MOYSIADIS, Karla PLEVOVÁ, Davide ROSSI, Jana KMÍNKOVÁ, Evangelia STALIKA a Lone BREDO PEDERSEN aj.

Vydání: Haematologica, PAVIA, FERRATA STORTI FOUNDATION, 2016, 0390-6078.

ISSN: 0390-6078, UT ISI: 000381941900019

Different spectra of recurrent gene mutations in subsets of chronic ... By combining data on recurrent gene mutations (BIRC3, MYD88 ... a subset-biased acquisition of gene mutations. More specifically, the frequency
https://is.muni.cz/publication/1355432

Association of Two Angiotensinogen Gene Polymorphisms (M235T and G(-6)A) with Chronic Heart Failure.

GOLDBERGOVÁ, Monika, Lenka ŠPINAROVÁ, Jindřich ŠPINAR, Jiří TOMAN, Anna VAŠKŮ a Jiří VÁCHA

Vydání: International Journal of Cardiology, Ireland, Elsevier, 2003, 0167-5273.

ISSN: 0167-5273, UT ISI: 000183429100018

Association of Two Angiotensinogen Gene Polymorphisms (M235T and ... relationship between the angiotensinogen (AGT) gene polymorphisms, M235T and ... of cardiovascular diseases. The AGT gene polymorphisms were detected by polymerase
https://is.muni.cz/publication/405279

Developmental regulation of the maize Zm-p60.1 gene encoding a beta-glucosidase located to plastids.

KRISTOFFERSEN, Peter, Břetislav BRZOBOHATÝ, HÖHFELD, Laszlo BAKO, Michael MELKONIAN a Klaus PALME

Vydání: Planta, Springer Berlin Heidelberg 2000, 2000, 0032-0935.

maize Zm-p60.1 gene encoding a beta-glucosidase located ... maize Zm-p60.1 gene. The expression of the Zm-p60.1 gene was analyzed by Northern blot
https://is.muni.cz/publication/242591

Pluripotent stem cells and gene therapy.

ŠIMARA, Pavel, Jason MOTL a Dan KAUFMAN

Vydání: Translational Research, 2013, 1931-5244.

ISSN: 1931-5244, UT ISI: 000316837400008

Pluripotent stem cells and gene therapy Human ... s cells. Current developments in gene modification methods have opened the ... generation techniques, as well as gene modification methods. We will then
https://is.muni.cz/publication/1094550

Association of the 5A/6A promoter polymorphism of the MMP-3 gene with the radiographic progression of rheumatoid arthritis.

NĚMEC, Petr, Monika PAVKOVA-GOLDBERGOVA, Jindra GATTEROVÁ, Anna VAŠKŮ a Miroslav SOUČEK

Vydání: Ann N Y Acad Sci. New York, USA, N Y Acad Sci, 2007, 0077-8923.

ISSN: 0077-8923, UT ISI: 000250428100020

polymorphism of the MMP-3 gene with the radiographic progression of ... polymorphism in the MMP-3 gene promoter can contribute to the ... polymorphism of the MMP-3 gene with radiographic progression of RA
https://is.muni.cz/publication/876456

Analysis of the COL7A1 gene in Czech patients with dystrophic epidermolysis bullosa reveals novel and recurrent mutations.

JEŘÁBKOVÁ, Barbora, Lenka KOPEČKOVÁ, Hana BUČKOVÁ, Karel VESELÝ, Jana VALÍČKOVÁ a Lenka FAJKUSOVÁ

Vydání: JOURNAL OF DERMATOLOGICAL SCIENCE, IRELAND, ELSEVIER IRELAND LTD, 2010, 0923-1811.

ISSN: 0923-1811, UT ISI: 000280675200010

the COL7A1 gene in Czech patients with dystrophic ... in the type VII collagen gene (COL7A1). The ... the COL7A1 gene and perform genotype-phenotype correlations
https://is.muni.cz/publication/913193

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