Trzeciak, Wiesław Henryk (1934- )
Trzeciak, Wiesław.
Wiesław Henryk Trzeciak
VIAF ID: 167365565 ( Personal )
Permalink: http://viaf.org/viaf/167365565
Preferred Forms
- 100 1 _ ‡a Trzeciak, Wieslaw
- 100 1 _ ‡a Trzeciak, Wiesław
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- 100 0 _ ‡a Wiesław Henryk Trzeciak
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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Biochemia | |
Clinical features, treatment and genetic background of Treacher Collins syndrome | |
Cloning of the lymphoid enhancer binding factor-1 (Lef-1) cDNA from rat kidney : homology to the mouse sequence | |
Contribution of protein kinase A and protein kinase C signalling pathways to the regulation of HSD11B2 expression and proliferation of MCF-7 cells | |
Decreased density of the CCR5 receptor on the surface of CD4+ lymphocytes and monocytes/macrophages is associated with the CCR5-59653T transition in the promoter region | |
The effect of indole-3-carbinol on the expression of CYP1A1, CYP1B1 and AhR genes and proliferation of MCF-7 cells | |
Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy | |
Geny syntaz tlenku azotu : struktura, regulacja ekspresji, produkty białkowe | |
Inhibition of CYP17 expression by adrenal androgens and transforming growth factor β in adrenocortical cells | |
Mechanizmy redagowania jądrowych mRNA | |
Molekularne i genetyczne podłoże idiopatycznej padaczki czołowej z napadami nocnymi | |
Molekularne podłoże wrodzonego braku zawiązków zębów stałych : na podstawie piśmiennictwa | |
A novel c.581C̃>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia? | |
A novel isoform of human lymphoid enhancer-binding factor-1 (LEF-1) gene transcript encodes a protein devoid of HMG domain and nuclear localization signal | |
Novel isoforms of transcript of the EDA gene confirm X-linked inheritance of anhidrotic ectodermal dysplasia | |
A novel mutation A1270G of the EDA1 gene causing Tyr343Cys substitution in ectodysplasin-A in a family with anhidrotic ectodermal dysplasia | |
Oxidative DNA damage and level of thiols as related to polymorphisms of MTHFR, MTR, MTHFD1 in Alzheimer's and Parkinson's diseases | |
Polymorphism in intron 23 of the endothelial nitric oxide synthase gene (NOS3) is not associated with hypertension | |
Przydatki skóry : wybrane zagadnienia | |
Recent advances in understanding of the molecular basis of anhidrotic ectodermal dysplasia : discovery of a ligand, ectodysplasin A and its two receptors | |
Le rôle des chimiokines et leurs récepteurs dans le développement de la phase effectrice de la réponse immunitaire antitumorale. | |
The role of chemokines and chemokine receptors in shaping the effector phase of anti-tumor immune response | |
Screening of chromosomal region 21q22.3 for mutations in genes associated with neuronal Ca²+ signalling in bipolar affective disorder | |
Steroidogenny czynnik-1 : struktura, mechanizm działania i rola biologiczna | |
Studies on CYP1A1, CYP1B1 and CYP3A4 gene polymorphisms in breast cancer patients | |
Temporal pattern of the induction of SF-1 gene expression by the signal transduction pathway involving 3',5'-cylic adenosine monophosphate | |
Transition C2718T in the AR gene, resulting in generation of a termination codon and truncated form of the androgen receptor, causes complete androgen insensitivity syndrome | |
The V3 region of gp120 is responsible for anti-HIV-1 activity of heparin sulphate | |
Znaczenie procesu apoptozy w patogenezie stwardnienia rozsianego |