Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Jaroslaw Jozwiak"'
Publikováno v:
Cell Transplantation, Vol 9 (2000)
Cartilage formed in transplants of allogeneic chondrocytes into joint cartilage defects in rats was infiltrated by immune cells migrating from the bone marrow while the surface on the side of the joint cavity remained free of infiltrations. This sugg
Externí odkaz:
https://doaj.org/article/cf4b4e5c595d4786aac4b0a722092cc1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Katarzyna Drapalo, Jaroslaw Jozwiak
Publikováno v:
The International journal of neuroscience. 128(2)
Ganglioglioma (GG) is a non-malignant tumor classified as G1 by the WHO. Although we currently know that the neoplasm may result from the hyperactivity of protein kinase B (PKB or Akt) or extracellular-regulated kinase (Erk), which upregulates mammal
Autor:
Jaroslaw Jozwiak, Agnieszka Zajaczkowska, Paweł Włodarski, Artur Slupianek, Wiesława Grajkowska, Katarzyna Kotulska, Marcin Roszkowski, Sergiusz Jozwiak, Wojciech Zalewski
Publikováno v:
NeuroMolecular Medicine. 9:117-127
Tuberous sclerosis (TS) is an autosomal dominant disease associated with the formation of usually benign tumors or hamartomas. The disease is connected with upregulation of mammalian target of rapamycin, central regulator of protein translation, whic
Publikováno v:
Medicinal Research Reviews. 27:869-890
Medulloblastoma is the most common malignant tumor of the cerebellum in children, with a tendency to metastasize via CSF pathway. Survival rate varies depending on several factors, but is rather favorable, with radiotherapy as the treatment of choice
Autor:
Paweł Włodarski, Jaroslaw Jozwiak
Publikováno v:
Journal of Neuro-Oncology. 79:229-234
Tuberous sclerosis, neurological genetic disorder characterized by the formation of benign tumors or hamartomas in multiple organ systems, is recently getting much attention. Numerous papers describe still-not-fully-explained pathogenesis of the dise
Publikováno v:
NeuroMolecular Medicine. 7:287-296
Tuberous sclerosis is an autosomal-dominant disorder caused by the mutation of one of the two tumor suppressor genes: TSC1 or TSC2, encoding protein products, hamartin, and tuberin, respectively. Both proteins form intracellular complexes exerting in
Autor:
Justyna Niderla, Jaroslaw Jozwiak, Stanislaw Moskalewski, Aldona Komar, Anna Hyc, Anna Osiecka-Iwan
Publikováno v:
Cell Transplantation, Vol 12 (2003)
Rat chondrocytes transplanted intramuscularly in rabbits produced cartilage. In 1-day-old transplants chondrocytes remained viable. After 1 week peripheral chondrocytes of the transplant were dead and the cartilage was surrounded and resorbed by macr
Publikováno v:
Transplantation Proceedings. 34:1079-1082