Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Roope A. Kallionpää"'
Autor:
Emma K. Rousi, Roope A. Kallionpää, Roosa E. Kallionpää, Susanna M. Juteau, Lauri A. I. Talve, Micaela M. Hernberg, Pia P. Vihinen, Veli-Matti Kähäri, Ilkka O. Koskivuo
Publikováno v:
Annals of Medicine, Vol 54, Iss 1, Pp 244-252 (2022)
Background Changes in the incidence of melanoma in children and adolescents have been reported in Europe and in the USA in the recent decades. Aims The aim of this study was to examine the incidence of paediatric and adolescent melanomas in Finland i
Externí odkaz:
https://doaj.org/article/a40c86903f8d40769a966df1c6d68722
Autor:
Jussi Leppävirta, Roope A. Kallionpää, Elina Uusitalo, Tero Vahlberg, Minna Pöyhönen, Juha Peltonen, Sirkku Peltonen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background Neurofibromatosis type 1 (NF1) is a dominantly inherited Rasopathy caused by mutations in the NF1 gene on chromosome 17. NF1 has been connected to congenital anomalies, e.g., in the skeletal and cardiovascular systems, but the ove
Externí odkaz:
https://doaj.org/article/fe5b25d702c94445a22f3701a43caf63
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Background Type 1 neurofibromatosis (NF1) is a genetic tumor predisposing Rasopathy. NF1 patients have an increased risk for developing benign and malignant tumors, but the occurrence of intestinal tumors has not been investigated at the pop
Externí odkaz:
https://doaj.org/article/fa4ef33f50ff477b832dbb18a28c9356
Autor:
Michael A. Tainsky, Ludwine M. Messiaen, Bruce R. Korf, Maria T. Acosta, Jaishri O. Blakeley, Sean J. Yoder, Zhihua Chen, Jacob P. Crowley, Renee N. Tousignant, Dhananjay A. Chitale, Patrick R. Gonzales, Roope A. Kallionpää, Xia Wang
TCGA invasive breast cancer mRNA expression, protein expression, and CNV comparison based on NF1 genetic alterations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29ce3190172e758502e024957eed668f
https://doi.org/10.1158/1940-6207.22533689.v1
https://doi.org/10.1158/1940-6207.22533689.v1
Autor:
Michael A. Tainsky, Ludwine M. Messiaen, Bruce R. Korf, Maria T. Acosta, Jaishri O. Blakeley, Sean J. Yoder, Zhihua Chen, Jacob P. Crowley, Renee N. Tousignant, Dhananjay A. Chitale, Patrick R. Gonzales, Roope A. Kallionpää, Xia Wang
Supplement 2 Figure. NF+BrCa OncoScan CNV Whole Genome Histogram.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0051e2e7b8328f14ccada86058206d8a
https://doi.org/10.1158/1940-6207.22533692.v1
https://doi.org/10.1158/1940-6207.22533692.v1
Autor:
Michael A. Tainsky, Ludwine M. Messiaen, Bruce R. Korf, Maria T. Acosta, Jaishri O. Blakeley, Sean J. Yoder, Zhihua Chen, Jacob P. Crowley, Renee N. Tousignant, Dhananjay A. Chitale, Patrick R. Gonzales, Roope A. Kallionpää, Xia Wang
IHC Validation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::042901a33289f6197d58367f6b7e47bf
https://doi.org/10.1158/1940-6207.22533695
https://doi.org/10.1158/1940-6207.22533695
Autor:
Roope A. Kallionpää, Juha O. Rinne, Kari Auranen, Mikko Valtanen, Juha Peltonen, Sirkku Peltonen, Elina Uusitalo
Publikováno v:
Genetics in Medicine
Purpose To determine the risk for dementia in neurofibromatosis type 1 (NF1) using a Finnish nationwide cohort of individuals with NF1, and data from national registries. Methods A Finnish cohort of 1,349 individuals with confirmed NF1 according to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ef2224f7e7f817fbe1f15cbca890ca
https://doi.org/10.1038/s41436-021-01261-3
https://doi.org/10.1038/s41436-021-01261-3
Autor:
Juha Peltonen, Eetu Heervä, Roope A. Kallionpää, Sirkku Peltonen, Paula Pennanen, Liisa Nissinen, Veli-Matti Kähäri
Publikováno v:
Molecular Biology Reports
Little is known about the signaling pathways involved in the differentiation of human osteoclasts. The present study evaluated the roles of the Ras/PI3K/Akt/mTOR, Ras/Raf/MEK1/2/ERK1/2, calcium-PKC, and p38 signaling pathways in human osteoclast diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63282689929b0bf89aeb5d11bd3971e6
https://doi.org/10.1007/s11033-020-06128-5
https://doi.org/10.1007/s11033-020-06128-5
Autor:
Sirkku Peltonen, Roope A. Kallionpää, Juha Peltonen, Hannu Järveläinen, Jussi Leppävirta, Kari Auranen, Minna Pöyhönen
Publikováno v:
Journal of Medical Genetics
BackgroundThe hereditary predisposition to diabetes is only partially explained by genes identified so far. Neurofibromatosis type 1 (NF1) is a rare monogenic dominant syndrome caused by aberrations of the NF1 gene. Here, we used a cohort of 1410 pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5edef69a046d2c1f2d3fe99aed52bf3b
http://europepmc.org/articles/PMC8142421
http://europepmc.org/articles/PMC8142421
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(4)
This study investigated whether individuals with neurofibromatosis 1 (NF1) fare worse than individuals without NF1 in terms of economic well-being. NF1 is relatively common in the population and provides an informative case of a rare hereditary disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9e92e45078caf4e6c8770078d045e61
https://pubmed.ncbi.nlm.nih.gov/34955382
https://pubmed.ncbi.nlm.nih.gov/34955382