Zobrazeno 1 - 10
of 340
pro vyhledávání: '"R. Herva"'
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-18 (2022)
Abstract Background Current understanding of the molecular basis of memory consolidation points to an important function of amyloid formation by neuronal-specific isoforms of the cytoplasmic polyadenylation element binding (CPEB) protein family. In p
Externí odkaz:
https://doaj.org/article/941e62766a19424c9a7e0f2ad942c863
Publikováno v:
Placenta. 26:387-392
The placenta is responsible for the production of progesterone (P) and estrogens during human pregnancy. In this study, the expression of several key steroidogenic enzymes was investigated in different cell types of human placenta during early and mi
Publikováno v:
International Journal of Sports Medicine. 23:610-615
We present a case report of acute bilateral excercise-induced compartment syndrome in the adductor longus muscles, which was treated with bilateral medial fasciotomies. Postoperatively, the healing process of the adductor muscles was followed up by r
Publikováno v:
Bone. 29:487-493
Fetal development and tumor progression both require a complex system of extracellular matrix (ECM) synthesis and breakdown, which is mediated by, for instance, the matrix metalloproteinases (MMPs). Human metalloelastase (MMP-12) is an MMP, the expre
Publikováno v:
British Journal of Dermatology. 158:646-648
Autor:
A. de la Chapelle, O Hovatta, Ulf-Håkan Stenman, Pekka Ylöstalo, K Juntunen, Kristiina Aittomäki, R Herva
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:3722-3726
The recent finding that a mutation in the FSH receptor gene causes ovarian dysgenesis prompted the present study to determine the phenotype caused by this mutation. Twenty-two patients with ovarian dysgenesis and a 566C--T mutation in the FSH recepto
Autor:
Katri Vuopala, R Herva
Publikováno v:
Journal of Medical Genetics. 31:521-527
In a national morphology based study of lethal arthrogryposis between 1979 and 1992, 40 fetuses and infants with lethal congenital contracture syndrome (LCCS, McKusick 253310) were found in Finland. The incidence of LCCS in Finland was 1:19,000 birth
Autor:
C. Aiello, N. Cannelli, J.D. Cooper, M. Haltia, R. Herva, U. Lahtinen, A.-E. Lehesjoki, S.E. Mole, F. M. Santorelli, E. Siintola, A. Simonati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78331c9170f34577b5de0fa0c192b685
https://doi.org/10.1093/med/9780199590018.003.0012
https://doi.org/10.1093/med/9780199590018.003.0012
Autor:
L, Skoglund, M, Viitanen, H, Kalimo, L, Lannfelt, M E, Jönhagen, M, Ingelsson, A, Glaser, R, Herva
Publikováno v:
European journal of neurology. 15(2)
Members of families with mutations in the tau gene are known to be heterogeneous in their clinical presentation, ranging from frontotemporal dementia to a clinical picture more resembling corticobasal degeneration or progressive supranuclear palsy. I
Publikováno v:
Reproduction (Cambridge, England). 126(3)
Investigation of the expression pattern of integrins and their extracellular matrix (ECM) ligands in trophoblasts at the maternal-fetal interface during tubal pregnancy may aid better understanding of the adhesion and invasion of acceptable maternal