Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Helena Ahola"'
1
Developing Business Models for the Underground Labs
Autor: Päivi Aro, Helena Ahola
DEVELOPING BUSINESS MODELS FOR THE UNDERGROUND LABS The purpose of this case study is to describe the process of developing business models for the underground labs (ULs) and their network in a Baltic Sea Interreg project (BSUIN). The RQs are the fol
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::549e519b36254915a6d7665b7e807904
https://doi.org/10.5194/egusphere-egu2020-1451
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5
Homozygous Variegate Porphyria: 20 y Follow-Up and Characterization of Molecular Defect
Autor: Shigeru Taketani, Raili Kauppinen, Kaisa Timonen, Eila Laitinen, Mikael von, Pertti Mustajoki, Helena Ahola, Raimo Tenhunen, und zu Fraunberg
Publikováno v: Journal of Investigative Dermatology. 116(4):610-613
The long-term follow-up of a homozygous variegate porphyria patient revealed severe photosensitivity accompanied by mild sensory neuropathy and IgA nephropathy. A 35T to C transition in exon 2 (I12T) and a 767C to G transversion in exon 7 (P256R) of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7383870d4fe6cb6e6b63aec31fcc8689
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6
Insertion of Alu element responsible for acute intermittent porphyria
Autor: Pertti Mustajoki, Sami Mustajoki, Helena Ahola, Raili Kauppinen
Publikováno v: Human mutation. 13(6)
In this study, we report a large Finnish family in which an Alu element interferes with the coding region of the porphobilinogen deaminase (PBGD) gene resulting in acute intermittent porphyria (AIP). Polymerase chain reaction (PCR) and single-strand
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::491cf718c91a4f6b4b235ffa713dd8c2
https://pubmed.ncbi.nlm.nih.gov/10408772
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7
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyria
Autor: Hannele Pihlaja, Raili Kauppinen, Pertti Mustajoki, Niels Erik Petersen, Sami Mustajoki, Helena Ahola
Publikováno v: Human genetics. 102(5)
Three splicing defects (IVS1+3G--T, 86A--T, IVS13-2A--G), an insertion (416insCA), and two missense mutations (664G--A and 833T--G) in the porphobilinogen deaminase (PBGD) gene were identified in six unrelated Finnish patients with acute intermittent
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef3f01f085442999beac80d92b5aec54
https://pubmed.ncbi.nlm.nih.gov/9654202
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8
Vegetated buffer zone project of the Vantaa River river basin
Autor: Helena Ahola
Publikováno v: Geografisk Tidsskrift-Danish Journal of Geography. 89:22-25
Ahola, Helena: Vegetated buffer zone project of the Vantaa River river basin. Geografisk Tidsskrift 89.22–25. Kobenhavn 1989. The purpose of this project is to find methods of examining vegetated buffer zones and erosion of river banks, to test tho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2def6e4c36dbb996ee844795dc4476e3
https://doi.org/10.1080/00167223.1989.10649277
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9
Conference
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