Výsledky vyhledávání - Marja Ojaniemi
- Zobrazuji výsledky 1 - 11 z 11
-
1
-
2
-
3
-
4
-
5
-
6
Age at adiposity rebound in childhood is associated with PCOS diagnosis and obesity in adulthood—longitudinal analysis of BMI data from birth to age 46 in cases of PCOS Autor Emilia Koivuaho, Johanna Laru, Marja Ojaniemi, Katri Puukka, Johannes Kettunen, Juha S. Tapanainen, Stephen Franks, Marjo‐Riitta Järvelin, Laure Morin‐Papunen, Sylvain Sebért, Terhi Piltonen
Vydáno 2019Artigo -
7
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2 Autor Heli Tiensuu, Antti M. Haapalainen, Minna K. Karjalainen, Anu Pasanen, Johanna M. Huusko, Riitta Marttila, Marja Ojaniemi, Louis J. Muglia, Mikko Hallman, Mika Rämet
Vydáno 2019Artigo -
8
Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis Autor Ritva Haataja, Minna K. Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P. Chaudhari, Jevon Plunkett, Jeffrey C. Murray, Steven A. McCarroll, Leena Peltonen, Louis J. Muglia, Aarno Palotie, Mikko Hallman
Vydáno 2011Artigo -
9
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort Autor Christoffer Löf, Konrad Patyra, Teemu Kuulasmaa, Jagadish Vangipurapu, Henriette Undeutsch, Holger Jaeschke, Tuulia Pajunen, Andreina Kero, Heiko Krude, Heike Biebermann, Gunnar Kleinau, Peter Kühnen, Krista Rantakari, Päivi J. Miettinen, Turkka Kirjavainen, Juha‐Pekka Pursiheimo, Taina Mustila, Jarmo Jääskeläinen, Marja Ojaniemi, Jorma Toppari, Jaakko Ignatius, Markku Laakso, Jukka Kero
Vydáno 2016Artigo -
10
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism Autor Hakan Cangül, Xiao-Hui Liao, Erik Schoenmakers, Jukka Kero, Sharon Barone, Panudda Srichomkwun, Hideyuki Iwayama, Eva Serra, Halil Sağlam, Erdal Eren, Ömer Tarım, Adeline K. Nicholas, Ilona Zvetkova, Carl A. Anderson, Fiona E. Karet, Kristien Boelaert, Marja Ojaniemi, Jarmo Jääskeläinen, Konrad Patyra, Christoffer Löf, E. D. Williams, Manoocher Soleimani, Timothy Barrett, Eamonn R. Maher, Krishna Chatterjee, Samuel Refetoff, Nadia Schoenmakers
Vydáno 2018Artigo -
11
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients Autor Liliya Rostomyan, Adrian Daly, Patrick Pétrossians, E. Nachev, Anurag Lila, Anne-Lise Lecoq, Beatriz Lecumberri, Giampaolo Trivellin, Roberto Salvatori, Andreas Moraitis, I. M. Holdaway, Dianne J Kranenburg - van Klaveren, Maria Chiara Zatelli, Nuria Palacios, Cécile Nozières, Margaret Zacharin, Tapani Ebeling, Marja Ojaniemi, Liudmila Rozhinskaya, Elisa Verrua, Marie‐Lise Jaffrain‐Rea, S. Filipponi, Daria Gusakova, Vyacheslav Pronin, Jérôme Bertherat, Zhanna Belaya, Irena Ilovayskaya, Mona Sahnoun-Fathallah, Caroline Sievers, Günter K. Stalla, Emilie Castermans, Jean-Hubert Caberg, Ekaterina Sorkina, Renata S. Auriemma, Sachin Mittal, Maria Kareva, Philippe A. Lysy, Philippe Émy, Ernesto De Menis, Catherine S. Choong, Giovanna Mantovani, Vincent Bours, Wouter de Herder, Thierry Brue, Anne Barlier, Sebastian Neggers, Sabina Zacharieva, Philippe Chanson, Nalini S. Shah, Constantine A. Stratakis, Luciana Ansaneli Naves, Albert Beckers
Vydáno 2015Artigo
Vyhledávací nástroje:
Související témata
Biology
Medicine
Internal medicine
Genetics
Cell biology
Chemistry
Signal transduction
Endocrinology
Environmental health
Gene
Population
Adapter molecule crk
Biochemistry
Congenital hypothyroidism
Cytokine
Fetus
Immunology
Phosphorylation
Placenta
Pregnancy
Proto-oncogene tyrosine-protein kinase Src
Receptor
Receptor tyrosine kinase
SH2 domain
Signal transducing adaptor protein
TLR4
Thyroid
Tyrosine kinase
Tyrosine phosphorylation
Amniotic fluid