Search Results - "Matěj, R"

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    Proteinase-activated receptor-2 expression in breast cancer and the role of trypsin on growth and metabolism of breast cancer cell line MDA MB-231 by Matej, R, Mandáková, P, Netíková, I, Poucková, P, Olejár, T

    Published in Physiological research (01-01-2007)
    “…Proteinase-activated receptor-2 (PAR-2) is a ubiquitous surface molecule participating in many biological processes. It belongs to the family of G…”
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    Human prion diseases in the Czech Republic by Rohan, Z, Rusina, R, Marešová, M, Matěj, R

    Published in Epidemiologie, mikrobiologie, imunologie (01-09-2015)
    “…Human prion diseases are a group of very rare diseases with a unique pathogenesis and, due to an inauspicious prognosis and unavailability of therapy, with…”
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    PAR2: The Cornerstone of Pancreatic Diseases by Suhaj, P, Olejar, T, Matej, R

    Published in Physiological research (31-10-2022)
    “…It has been 30 years since the first member of the protease-activated receptor (PAR) family was discovered. This was followed by the discovery of three other…”
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    PAR2 knock-out C57Bl6 mice as a model for evaluating metastases of cancer cells: pilot in vivo study of the metastatic potential of B16 melanoma in knock-out (PAR2-/-) animals by Matěj, R, Zadinová, M, Poučková, P, Kukal, J, Olejár, T

    Published in Folia biologica (2012)
    “…Proteinase-activated receptor 2 (PAR-2) is a ubiquitous surface molecule. It belongs to the family of G protein-coupled receptors activated by site-specific…”
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    PPY-cell hyperplasia accompanying NENs: Immunohistochemical and nuclear medicine analysis by Suhaj, P., Do, D., Olejar, T., Pichova, R., Lang, O., Matej, R.

    Published in Pathology, research and practice (01-01-2024)
    “…Pancreatic polypeptide cell hyperplasia (PPY-H) is a multiplication of the neuroendocrine cells producing pancreatic polypeptide (PPY). The development and…”
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    Relationship between ALS and the degree of cognitive impairment, markers of neurodegeneration and predictors for poor outcome. A prospective study by Rusina, R., Ridzoň, P., Kulišt'ák, P., Keller, O., Bartoš, A., Buncová, M., Fialová, L., Koukolík, F., Matěj, R.

    Published in European journal of neurology (01-01-2010)
    “…Introduction:  Amyotrophic lateral sclerosis (ALS) is a common neurodegenerative disease affecting motor neurons and may be associated with impaired cognition…”
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    Differential expression and processing of matrix metalloproteinase 19 marks progression of gastrointestinal diseases by Cervinková, M, Horák, P, Kanchev, I, Matěj, R, Fanta, J, Sequens, R, Kašpárek, P, Sarnová, L, Turečková, J, Sedláček, R

    Published in Folia biologica (01-01-2014)
    “…Matrix metalloproteinases (MMPs), responsible for extracellular matrix remodelling and processing of numerous soluble and cell-surface proteins, appear to play…”
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    Proteinase-activated receptor-2 expression on cerebral neurones after radiation damage: immunohistochemical observation in Wistar rats by Olejár, T, Matĕj, R, Zadinová, M, Poucková, P

    “…Radiation damage results in blood-brain barrier damage followed by blood plasma transfer into the neuropil. The transferred liquid contains high amounts of…”
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    Amyotrophic lateral sclerosis and Alzheimer's disease - clinical and neuropathological considerations in two cases by Rusina, R., Sheardová, K., Rektorová, I., Ridzoň, P., Kulišt'ák, P., Matěj, R.

    Published in European journal of neurology (01-07-2007)
    “…Amyotrophic lateral sclerosis (ALS) may be accompanied by cognitive impairment; when present, it is mainly in the form of frontotemporal impairment. We report…”
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    Anterior opercular syndrome in frontotemporal lobar degeneration with ubiquitin-only immunoreactive neuronal changes by Rektorova, I., Matej, R.

    Published in European journal of neurology (01-06-2007)
    “…This paper presents for the first time an anterior opercular syndrome in association with a gait disorder, dropped head syndrome, dysphagia, and sialorrhea in…”
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    Acute pancreatitis: proteinase-activated receptor-2 as Dr. Jekyll and Mr. Hyde by Matej, R, Housa, D, Olejár, T

    Published in Physiological research (01-01-2006)
    “…"Proteinase-activated" receptor-2 (PAR-2) is a G protein-coupled transmembrane receptor with seven transmembrane domains activated by trypsin. It has been…”
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    Multiple system atrophy and Alzheimer's disease: a case report of a rare association of two neuro-degenerative disorders by Rusina, R, Bourdain, F, Matej, R

    Published in Revue neurologique (01-12-2007)
    “…Multiple system atrophy (MSA) is a neurodegenerative disorder typically characterised by cerebellar dysfunction, parkinsonism, pyramidal signs and dysautonomy…”
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    Evaluation of safe resection margins in tumours of parenchymatous organs by Hermanová, M, Matěj, R, Dušková, J, Honsová, E, Tichý, M

    Published in Rozhledy v chirurgii (01-02-2014)
    “…The definition of a safe surgical margin in tumours of parenchymatous organs has been the subject of frequent debates and a number of studies. This topic is…”
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    Evaluation of Inflammatory Cells (Tumor Infiltrating Lymphocytes) in Solid Tumors by Dundr, P, Němejcová, K, Bártů, M, Matěj, R, Rohan, Z, Tichá, I

    Published in Klinická onkologie (2017)
    “…The tumor microenvironment plays an important role in tumorigenesis and the tumor-host relationship. An important part of the tumor microenvironment is…”
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    Retrospective sequence analysis of the human PRNP gene from the formaldehyde-fixed paraffin-embedded tissues: report of two cases of Creutzfeldt-Jakob disease by Sikora, J, Srbová, A, Koukolík, F, Matej, R

    Published in Folia microbiologica (2006)
    “…The definitive diagnosis of the CJD (Creutzfeldt-Jakob disease; very rare neurodegenerative disorder) can be established only on the basis of post-mortem…”
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    Argyrophilic grain disease: case report of the first two cases in the Czech Republic and review of the literature by Matĕj, R, Koukolík, F

    Published in Ceskoslovenské patologie (01-04-2006)
    “…Argyrophilic grain disease (AgD) is a relatively newly described neurodegenerative disease with late-onset dementia. Morphologically it is characterized by the…”
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