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Metin Özata

university of hamburg

39H指数
134论文数
7.5K被引数
收录论文 40
发表时间
Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms
err2023-02-08
err4
errOAAI
errCassin, 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
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Impact of glucocorticoid receptor gene (NR3C1) polymorphisms in Turkish patients with metabolic syndrome
err2015-11-23
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PREAI
errKaya, Z.; Caglayan, S.; Akkiprik, M.; Aral, C.; Ozisik, G.; Ozata, M.; Ozer, A.
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The effects of thyroid status on plasma leptin levels in women
err2014-04-11
err41
PREAI
errOzata, M; Ozisik, G; Bingol, N; Corakci, A; Gundogan, MA
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Evaluation of central motor conduction in hypothyroid and hyperthyroid patients
err2014-04-04
err7
PREAI
errOzata, M; Ozkardes, A; Dolu, H; Corakci, A; Yardim, M; Gundogan, MA
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Event-related brain potentials in male hypogonadism
err2014-03-11
err9
PREAI
errOzata, M; Odabasi, Z; Caglayan, S; Beyhan, Z; Vural, O; Ozdemir, C
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Prevalence of the DNA repair enzyme-NEIL1 gene mutation in patients with Type 2 diabetes in the Turkish population
err2012-04-01
err5
PREAI
errSalmanoglu, M.; Kucukardali, Y.; Kucukodaci, Z.; Fenercioglu, A.; Solmazgul, E.; Onem, Y.; Baloglu, H.; Ozata, M.
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GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants in KISS1/Kiss1
err2011-11-01
err52
errOAAI
errChan, 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.
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WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
err2010-10-01
err156
errOAAI
errKim, 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.
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TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood
err2010-06-01
err210
errOAAI
errGianetti, 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.
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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
err2008-10-01
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errOAAI
errKim, 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.
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KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans
err2007-01-09
err36
errOAAI
errBhagavath, Balasubramanian; Xu, Ning; Ozata, Metin; Rosenfield, Robert L.; Bick, David P.; Sherins, Richard J.; Layman, Lawrence C.
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Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism
err2006-11-01
err67
PREAI
errCerrato, 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.
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Leptin, soluble interleukin-6 receptor, C-reactive protein and soluble vascular cell adhesion molecule-1 levels in human coronary atherosclerotic plaque
err2006-02-16
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errOAAI
errKaraduman, 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
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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
err2006-01-04
err28
PREAI
errKaraduman, M; Sengul, A; Oktenli, C; Pekel, A; Yesilova, Z; Musabak, U; Sanisoglu, SY; Gunay, C; Baysan, O; Kocar, IH; Tatar, H; Ozata, M
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Effect of leptin replacement on brain structure in genetically leptin-deficient adults
err2005-05-01
err153
errOAAI
errMatochik, JA; London, ED; Yildiz, BO; Ozata, M; Caglayan, S; DePaoli, AM; Wong, ML; Licinio, J
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Increased acylation stimulating protein concentrations in nonalcoholic fatty liver disease are associated with insulin resistance
err2005-04-01
err47
PREAI
errYesilova, Z; Ozata, M; Oktenli, C; Bagci, S; Ozcan, A; Sanisoglu, SY; Uygun, A; Yaman, H; Karaeren, N; Dagalp, K
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The association of plasma adiponectin levels with hypertensive retinopathy
err2005-02-01
err34
errOAAI
errYilmaz, MI; Sonmez, A; Kilic, S; Celik, T; Bingol, N; Pinar, M; Mumcuoglu, T; Ozata, M
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