Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maria Rife"'
Publikováno v:
The Journal of Immunology. 206:20.33-20.33
House dust mites (HDM) are a predominant causative agent of airway hypersensitivity and asthma. The HDM group 1 allergens include Der p 1, a cysteine protease that contributes to sensitization and symptom exacerbation. Respiratory syncytial virus (RS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c11b1b57d66c67204105611e6ab3c39
https://doi.org/10.4049/jimmunol.206.supp.20.33
https://doi.org/10.4049/jimmunol.206.supp.20.33
Autor:
Ben A. Oostra, Laura L. Kirkpatrick, Marianne Hoogeveen-Westerveld, Lies-Anne A. Severijnen, Ruben H. Willemsen, T. Zu, David L. Nelson, Ingeborg M. Nieuwenhuizen, Edwin Mientjes, Maria Rife
Publikováno v:
Neurobiology of Disease, Vol 21, Iss 3, Pp 549-555 (2006)
Neurobiology of Disease, 21(3), 549-555. Academic Press
Neurobiology of Disease, 21(3), 549-555. Academic Press
The FMR1 gene, mutated in Fragile X syndrome patients, has been modeled in mice with a neomycin cassette inserted in exon 5 of the mouse Fmr1 gene creating an Fmr1 knockout (Fmr1 KO) allele. This results in animals lacking Fmr1 protein (Fmrp) express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::996e7d6c9e5def9f50d041480af0d8bd
https://doi.org/10.1016/j.nbd.2005.08.019
https://doi.org/10.1016/j.nbd.2005.08.019
Autor:
Sandra van 't Padje, Ben A. Oostra, Mariëtte Schrier, Gert van Cappellen, Maria Rife, Lies-Anne Severijnen, Surya A. Reis, Rob Willemsen
Publikováno v:
Experimental Neurology, 189, 343-353. Academic Press
Lack of fragile X mental retardation protein (FMRP) causes the fragile X syndrome, a common form of inherited mental retardation. The syndrome usually results from the expansion of a CGG repeat in the FMR1 gene with consequent transcriptional silenci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b849cc80b81b70c760b3f979e32215f
https://pure.eur.nl/en/publications/8be8df22-db38-407d-aa98-5c35bcdd4ab4
https://pure.eur.nl/en/publications/8be8df22-db38-407d-aa98-5c35bcdd4ab4
Autor:
Rob Willemsen, Josien Levenga, Ronald A.M. Buijsen, Maria Rife, Ben A. Oostra, David L. Nelson, Femke M.S. de Vrij, Hervé Moine
Publikováno v:
Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2009, 35 (2), pp.241-50. ⟨10.1016/j.nbd.2009.05.004⟩
Neurobiology of Disease, 35(2), 241-250. Academic Press
Neurobiology of Disease, Vol 35, Iss 2, Pp 241-250 (2009)
Neurobiology of Disease, 2009, 35 (2), pp.241-50. ⟨10.1016/j.nbd.2009.05.004⟩
Neurobiology of Disease, Elsevier, 2009, 35 (2), pp.241-50. ⟨10.1016/j.nbd.2009.05.004⟩
Neurobiology of Disease, 35(2), 241-250. Academic Press
Neurobiology of Disease, Vol 35, Iss 2, Pp 241-250 (2009)
Neurobiology of Disease, 2009, 35 (2), pp.241-50. ⟨10.1016/j.nbd.2009.05.004⟩
Fragile X syndrome is caused by lack of the protein FMRP. FMRP mediates mRNA binding, dendritic mRNA transport and translational control at spines. We examined the role of functional domains of FMRP in neuronal RNA-granule formation and dendritic tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::649c484f53cde5b703cb3668263a57eb
https://www.hal.inserm.fr/inserm-00420367
https://www.hal.inserm.fr/inserm-00420367
Publikováno v:
Blood. 108:1922-1922
Immortal cell growth is considered the hallmark of tumor cells. In contrast, normal cells have a limited proliferative capacity of 40–60 cell divisions, also known as the Hayflick limit. The limited proliferative capacity of normal cells relates to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f81d6ace5d1f0a799d6e5bc63654eea
https://doi.org/10.1182/blood.v108.11.1922.1922
https://doi.org/10.1182/blood.v108.11.1922.1922
Autor:
Josien Levenga, Ronald A.M. Buijsen, Maria Rifé, Hervé Moine, David L. Nelson, Ben A. Oostra, Rob Willemsen, Femke M.S. de Vrij
Publikováno v:
Neurobiology of Disease, Vol 35, Iss 2, Pp 241-250 (2009)
Fragile X syndrome is caused by lack of the protein FMRP. FMRP mediates mRNA binding, dendritic mRNA transport and translational control at spines. We examined the role of functional domains of FMRP in neuronal RNA-granule formation and dendritic tra
Externí odkaz:
https://doaj.org/article/d58d87658b9d4e1fb6e0706e5be2a970