未登录 Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms Cassin, Jessica; Stamou, Maria I.; Keefe, Kimberly W.; Sung, Kaitlin E.; Bojo, Celine C.; Tonsfeldt, Karen J.; Rojas, Rebecca A.; Lopes, Vanessa Ferreira; Plummer, Lacey; Salnikov, Kathryn B.; Keefe, David L.; Ozata, Metin; Genel, Myron; Georgopoulos, Neoklis A.; Hall, Janet E.; Crowley, William F., Jr.; Seminara, Stephanie B.; Mellon, Pamela L.; Balasubramanian, Ravikumar 分享 收藏
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GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants in KISS1/Kiss1 Chan, Yee-Ming; Broder-Fingert, Sarabeth; Paraschos, Sophia; Lapatto, Risto; Au, Margaret; Hughes, Virginia; Bianco, Suzy D. C.; Min, Le; Plummer, Lacey; Cerrato, Felecia; De Guillebon, Adelaide; Wu, I-Hsuan; Wahab, Fazal; Dwyer, Andrew; Kirsch, Susan; Quinton, Richard; Cheetham, Timothy; Ozata, Metin; Ten, Svetlana; Chanoine, Jean-Pierre; Pitteloud, Nelly; Martin, Kathryn A.; Schiffmann, Raphael; Van der Kamp, Hetty J.; Nader, Shahla; Hall, Janet E.; Kaiser, Ursula B.; Seminara, Stephanie B. 分享 收藏
WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome Kim, Hyung-Goo; Ahn, Jang-Won; Kurth, Ingo; Ullmann, Reinhard; Kim, Hyun-Taek; Kulharya, Anita; Ha, Kyung-Soo; Itokawa, Yasuhide; Meliciani, Irene; Wenzel, Wolfgang; Lee, Deresa; Rosenberger, Georg; Ozata, Metin; Bick, David P.; Sherins, Richard J.; Nagase, Takahiro; Tekin, Mustafa; Kim, Soo-Hyun; Kim, Cheol-Hee; Ropers, Hans-Hilger; Gusella, James F.; Kalscheuer, Vera; Choi, Cheol Yong; Layman, Lawrence C. 分享 收藏
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood Gianetti, Elena; Tusset, Cintia; Noel, Sekoni D.; Au, Margaret G.; Dwyer, Andrew A.; Hughes, Virginia A.; Abreu, Ana Paula; Carroll, Jessica; Trarbach, Ericka; Silveira, Leticia F. G.; Costa, Elaine M. F.; de Mendonca, Berenice Bilharinho; de Castro, Margaret; Lofrano, Adriana; Hall, Janet E.; Bolu, Erol; Ozata, Metin; Quinton, Richard; Amory, John K.; Stewart, Susan E.; Arlt, Wiebke; Cole, Trevor R.; Crowley, William F.; Kaiser, Ursula B.; Latronico, Ana Claudia; Seminara, Stephanie B. 分享 收藏
Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome Kim, Hyung-Goo; Kurth, Ingo; Lan, Fei; Meliciani, Irene; Wenzel, Wolfgang; Eom, Soo Hyun; Kang, Gil Bu; Rosenberger, Georg; Tekin, Mustafa; Ozata, Metin; Bick, David P.; Sherins, Richard J.; Walker, Steven L.; Shi, Yang; Gusella, James F.; Layman, Lawrence C. 分享 收藏
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Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism Cerrato, Felecia; Shagoury, Jenna; Kralickova, Milena; Dwyer, Andrew; Falardeau, John; Ozata, Metin; Van Vliet, Guy; Bouloux, Pierre; Hall, Janet E.; Hayes, Frances J.; Pitteloud, Nelly; Martin, Kathryn A.; Welt, Corrine; Seminara, Stephanie B. 分享 收藏
Leptin, soluble interleukin-6 receptor, C-reactive protein and soluble vascular cell adhesion molecule-1 levels in human coronary atherosclerotic plaque Karaduman, M; Oktenli, C; Musabak, U; Sengul, A; Yesilova, Z; Cingoz, F; Olgun, A; Sanisoglu, SY; Baysan, O; Yildiz, O; Taslipinar, A; Tatar, H; Kutlu, M; Ozata, M 分享 收藏
Tissue levels of adiponectin, tumour necrosis factor-alpha, soluble intercellular adhesion molecule-1 and heart-type fatty acid-binding protein in human coronary atherosclerotic plaques Karaduman, M; Sengul, A; Oktenli, C; Pekel, A; Yesilova, Z; Musabak, U; Sanisoglu, SY; Gunay, C; Baysan, O; Kocar, IH; Tatar, H; Ozata, M 分享 收藏
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Increased acylation stimulating protein concentrations in nonalcoholic fatty liver disease are associated with insulin resistance Yesilova, Z; Ozata, M; Oktenli, C; Bagci, S; Ozcan, A; Sanisoglu, SY; Uygun, A; Yaman, H; Karaeren, N; Dagalp, K 分享 收藏
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