Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

Por Pitteloud, Nelly, Zhang, Chengkang, Pignatelli, Duarte, Li, Jia-Da, Raivio, Taneli, Cole, Lindsay W., Plummer, Lacey, Jacobson-Dickman, Elka E., Mellon, Pamela L., Zhou, Qun-Yong, Crowley, William F.
Publicado em 2007

Mutations in Prokineticin 2 and Prokineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

Por Cole, Lindsay W., Sidis, Yisrael, Zhang, ChengKang, Quinton, Richard, Plummer, Lacey, Pignatelli, Duarte, Hughes, Virginia A., Dwyer, Andrew A., Raivio, Taneli, Hayes, Frances J., Seminara, Stephanie B., Huot, Celine, Alos, Nathalie, Speiser, Phyllis, Takeshita, Akira, VanVliet, Guy, Pearce, Simon, Crowley, William F., Zhou, Qun-Yong, Pitteloud, Nelly
Publicado em 2008

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

Por Falardeau, John, Chung, Wilson C.J., Beenken, Andrew, Raivio, Taneli, Plummer, Lacey, Sidis, Yisrael, Jacobson-Dickman, Elka E., Eliseenkova, Anna V., Ma, Jinghong, Dwyer, Andrew, Quinton, Richard, Na, Sandra, Hall, Janet E., Huot, Celine, Alois, Natalie, Pearce, Simon H.S., Cole, Lindsay W., Hughes, Virginia, Mohammadi, Moosa, Tsai, Pei, Pitteloud, Nelly
Publicado em 2008