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Taneli Raivio

Showing results (61-70 of 134) with videos related to

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European Journal of Human Genetics : EJHG|March 20, 2023
Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scoresMaria Siermann, Ophelia Valcke, Joris Robert Vermeesch, et al.
Social Science & Medicine (1982)|January 20, 2024
"Are we not going too far?": Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionalsMaria Siermann, Ophelia Valcke, Joris Robert Vermeesch, et al.
Disease Models & Mechanisms|July 14, 2022
FGF8-FGFR1 signaling regulates human GnRH neuron differentiation in a time- and dose-dependent mannerVenkatram Yellapragada, Nazli Eskici, Yafei Wang, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Activation of the bone morphogenetic protein signaling pathway induces inhibin beta(B)-subunit mRNA and secreted inhibin B levels in cultured human granulosa-luteal cellsRisto Jaatinen, Jonas Bondestam, Taneli Raivio, et al.
Pediatric Research|April 28, 2006
Are adolescent boys with Klinefelter syndrome androgen deficient? A longitudinal study of Finnish 47,XXY boysAnne M Wikström, Leo Dunkel, Sanna Wickman, et al.
BMC Research Notes|September 24, 2011
LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious pubertyJohanna Tommiska, Kaspar Sørensen, Lise Aksglaede, et al.
Orphanet Journal of Rare Diseases|June 21, 2011
Incidence, phenotypic features and molecular genetics of Kallmann syndrome in FinlandEeva-Maria Laitinen, Kirsi Vaaralahti, Johanna Tommiska, et al.
European Journal of Endocrinology|December 23, 2011
Decrease in circulating fibroblast growth factor 21 after an oral fat load is related to postprandial triglyceride-rich lipoproteins and liver fatNiina Matikainen, Marja-Riitta Taskinen, Sanna Stennabb, et al.
Pediatric Research|April 29, 2014
De novo SOX10 nonsense mutation in a patient with Kallmann syndrome and hearing lossKirsi Vaaralahti, Johanna Tommiska, Vallo Tillmann, et al.
Reproductive Biomedicine Online|July 18, 2024
Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screeningMaria Siermann, Joris R Vermeesch, Taneli Raivio, et al.
Pageof 14

Showing results (61-70 of 134) with videos related to

Sort By:
Pageof 14
European Journal of Human Genetics : EJHG|March 20, 2023
Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scoresMaria Siermann, Ophelia Valcke, Joris Robert Vermeesch, et al.
Social Science & Medicine (1982)|January 20, 2024
"Are we not going too far?": Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionalsMaria Siermann, Ophelia Valcke, Joris Robert Vermeesch, et al.
Disease Models & Mechanisms|July 14, 2022
FGF8-FGFR1 signaling regulates human GnRH neuron differentiation in a time- and dose-dependent mannerVenkatram Yellapragada, Nazli Eskici, Yafei Wang, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Activation of the bone morphogenetic protein signaling pathway induces inhibin beta(B)-subunit mRNA and secreted inhibin B levels in cultured human granulosa-luteal cellsRisto Jaatinen, Jonas Bondestam, Taneli Raivio, et al.
Pediatric Research|April 28, 2006
Are adolescent boys with Klinefelter syndrome androgen deficient? A longitudinal study of Finnish 47,XXY boysAnne M Wikström, Leo Dunkel, Sanna Wickman, et al.
BMC Research Notes|September 24, 2011
LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious pubertyJohanna Tommiska, Kaspar Sørensen, Lise Aksglaede, et al.
Orphanet Journal of Rare Diseases|June 21, 2011
Incidence, phenotypic features and molecular genetics of Kallmann syndrome in FinlandEeva-Maria Laitinen, Kirsi Vaaralahti, Johanna Tommiska, et al.
European Journal of Endocrinology|December 23, 2011
Decrease in circulating fibroblast growth factor 21 after an oral fat load is related to postprandial triglyceride-rich lipoproteins and liver fatNiina Matikainen, Marja-Riitta Taskinen, Sanna Stennabb, et al.
Pediatric Research|April 29, 2014
De novo SOX10 nonsense mutation in a patient with Kallmann syndrome and hearing lossKirsi Vaaralahti, Johanna Tommiska, Vallo Tillmann, et al.
Reproductive Biomedicine Online|July 18, 2024
Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screeningMaria Siermann, Joris R Vermeesch, Taneli Raivio, et al.
Pageof 14