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P. Hartmann

As seen in: Color Research & Application, Abendzeitung
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Articles by P. Hartmann

Tak prezentowały się placówki naszego regionu podczas Giełdy Szkół!

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By P. Hartmann
| mojakruszwica.pl
Materiał ABCJanikowo24.pl: 27 marca w Janikowie zorganizowano Giełdę Szkół Ponadpodstawowych, skierowaną do uczniów klas VIII, którzy w najbliższym czasie będą podejmować decyzję o wyborze dalszej ścieżki edukacyjnej. Wydarzenie odbyło się w Hali Widowiskowo-Sportowej przy ul. Głównej 40. W spotkaniu uczestniczyły szkoły ponadpodstawowe z powiatów inowrocławskiego i mogileńskiego.
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Black lives matter in München: Weiter friedlich und wütend

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By P. Hartmann, R. Hub
| Abendzeitung Verified
Demonstrantinnen und Polizei auf der Theresienwiese. Foto: Petra Schramek Es sind nicht mehr Zehntausende, die mit Black lives matter in München auf die Straße gehen. Aber der Protest ist "kein Zwei-Wochen-Thema". München – "Nur weil Rassismus verboten ist, heißt das nicht, dass er nicht existiert", sagt Redner Jiréh bei der Eröffnung der Black-lives-matter-Demonstration am Samstagabend auf der Theresienwiese.
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Expression profile of pattern recognition receptors in skeletal muscle of SOD1(G93A) amyotrophic lateral sclerosis (ALS) mice and sporadic ALS patients - Lehmann - - Neuropathology and Applied Neurobiology - Wiley Online Library

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By S. Lehmann, A. Goswami, E. Esch, P. Hartmann
| Color Research & Application Verified
Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of motoneurons and progressive muscle wasting. Inflammatory processes, mediated by non‐neuronal cells, such as glial cells, are known to contribute to disease progression. Inflammasomes consist of pattern recognition receptors (PRRs), apoptosis‐associated speck‐like protein (ASC) and caspase 1 and are essential for interleukin (IL) processing and a rapid immune response after tissue damage.
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Expression profile of pattern recognition receptors in skeletal muscle of SOD1(G93A) amyotrophic lateral sclerosis (ALS) mice and sporadic ALS patients - Lehmann - 2018 - Neuropathology and Applied Neurobiology - Wiley Online Library

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By S. Lehmann, E. Esch, P. Hartmann, A. Goswami
| Color Research & Application Verified
Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of motoneurons and progressive muscle wasting. Inflammatory processes, mediated by non‐neuronal cells, such as glial cells, are known to contribute to disease progression. Inflammasomes consist of pattern recognition receptors (PRRs), apoptosis‐associated speck‐like protein (ASC) and caspase 1 and are essential for interleukin (IL) processing and a rapid immune response after tissue damage.
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