Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kirsi Vaaralahti"'
Autor:
Johanna Tommiska, Eeva-Maria Laitinen, Karoliina Wehkalampi, Taneli Raivio, Kirsi Vaaralahti, Leo Dunkel
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 95:3063-3066
Background: Recently variation in LIN28B, a human ortholog of the gene-regulating processing of micro-RNAs (miRNAs) controlling the timing of major developmental events in the nematode Caenorhabtidis elegans, was reported to be associated with timing
Autor:
Nelly Pitteloud, Peter Hackman, Johanna Känsäkoski, Eeva-Maria Laitinen, Taneli Raivio, Kirsi Vaaralahti, Johanna Tommiska, Rainer Fagerholm
Publikováno v:
Pediatric research. 75(5)
Congenital hypogonadotropic hypogonadism (HH), a rare disorder characterized by absent, partial, or delayed puberty, can be caused by the lack or deficient number of hypothalamic gonadotropin-releasing hormone (GnRH) neurons. SEMA3A was recently impl
Autor:
Jorma Toppari, Kirsi Vaaralahti, Johanna Tommiska, Helena E. Virtanen, Heidi Oehlandt, Rosanna Koivu, Taneli Raivio, Eeva-Maria Laitinen
Publikováno v:
Molecular and Cellular Endocrinology
Molecular and Cellular Endocrinology, Elsevier, 2011, 341 (1-2), pp.35. ⟨10.1016/j.mce.2011.05.015⟩
Molecular and Cellular Endocrinology, Elsevier, 2011, 341 (1-2), pp.35. ⟨10.1016/j.mce.2011.05.015⟩
Mutations in FGFR1 , GNRHR , PROK2 , PROKR2 , TAC3 , or TACR3 underlie isolated hypogonadotropic hypogonadism (IHH) with clinically variable phenotypes, and, by causing incomplete intrauterine activation of the hypothalamic–pituitary–gonadal axis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb55faac50bfc21d563c745856215f26
https://hal.archives-ouvertes.fr/hal-00719875/document
https://hal.archives-ouvertes.fr/hal-00719875/document
Autor:
Kirsi Vaaralahti, Vallo Tillmann, Johanna Känsäkoski, Natalja Liivak, Johanna Tommiska, Taneli Raivio, Eeva-Maria Laitinen
Publikováno v:
Pediatric Research. 76:115-116
Autor:
Eeva-Maria Laitinen, Taneli Raivio, Karoliina Wehkalampi, Johanna Tommiska, Leo Dunkel, Kirsi Vaaralahti
Publikováno v:
Fertility and sterility. 95(8)
Variation in FGFR1, GNRHR, TAC3, and TACR3 was evaluated in 146 Finnish subjects with constitutional delay of growth and puberty. Although one male subject carried a previously undescribed heterozygous deletion (Phe309del) in GNRHR, which segregated