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The Journal of Clinical Endocrinology and Metabolism|March 24, 2005
Estrogen receptors and estrogen-metabolizing enzymes in human ovaries during fetal developmentTommi E Vaskivuo, Minna Mäentausta, Svea Törn, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 7, 2004
Expression of collagen XVIII and MMP-20 in developing teeth and odontogenic tumorsAnu Väänänen, Leo Tjäderhane, Lauri Eklund, et al.
Brain : a Journal of Neurology|September 30, 2008
Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndromeAlexandra Götz, Pirjo Isohanni, Helena Pihko, et al.
Fertility and Sterility|July 4, 2002
Effects of follicle-stimulating hormone (FSH) and human chorionic gonadotropin in individuals with an inactivating mutation of the FSH receptorTommi E Vaskivuo, Kristiina Aittomäki, Mikko Anttonen, et al.
Journal of Neuropathology and Experimental Neurology|September 20, 2017
Germline MSH6 Mutation in a Patient With Two Independent Primary GlioblastomasLinda M Forsström, Koichiro Sumi, Markus J Mäkinen, et al.
Nature Genetics|January 22, 2008
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron diseaseHeidi O Nousiainen, Marjo Kestilä, Niklas Pakkasjärvi, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 31, 2003
Expression of P450 aromatase and 17beta-hydroxysteroid dehydrogenase type 1 at fetal-maternal interface during tubal pregnancyYan Li, Li Qin, Zhi-Jie Xiao, et al.
Epilepsy Research|April 11, 2009
Digenic mutations in severe myoclonic epilepsy of infancyMaija Bolszak, Anna-Kaisa Anttonen, Tuomas Komulainen, et al.
Epilepsia|February 26, 2008
Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticusJohanna Uusimaa, Reetta Hinttala, Heikki Rantala, et al.
American Journal of Human Genetics|March 6, 2012
Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cystsAnne Polvi, Tarja Linnankivi, Tero Kivelä, et al.
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