Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Gokhan Ozisik"'
Autor:
Cenk Aral, Mustafa Akkiprik, Gokhan Ozisik, Ali Haydar Özer, S. Caglayan, Zehra Kaya, Metin Ozata
WOS: 000374102700010 PubMed ID: 26596278 Background The metabolic syndrome (MetS) is characterized by a cluster of metabolic factors, including insulin resistance and type-2 diabetes, abdominal obesity, dyslipidemia, hypertension and microalbuminuria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb92b457c48b3d36806c56b4496f398
https://avesis.yyu.edu.tr/publication/details/695dc9a0-7a4f-423d-86ec-a87d19216030/oai
https://avesis.yyu.edu.tr/publication/details/695dc9a0-7a4f-423d-86ec-a87d19216030/oai
Publikováno v:
Expert Opinion on Therapeutic Patents. 17:137-145
At present, the most widely used medications for controlled ovarian hyperstimulation (COH) include clomifene citrate (CC) and gonadotropins. CC is a safe, effective and cheap agent for COH; however, antiestrogenic effects on endometrium and cervical
Autor:
Gokhan Ozisik, J. Larry Jameson, Wen-Xia Gu, John C. Achermann, Lin Lin, Wing S. To, Catherine J. Owen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:3048-3054
Context: Primary adrenal failure is a life-threatening condition that can be caused by a range of etiologies, including autoimmune, metabolic, and developmental disorders. The nuclear receptors DAX1 (NR0B1) and steroidogenic factor-1 (SF1/Ad4BP, NR5A
Autor:
Giovanna Mantovani, Jeffrey Weiss, Paolo Beck-Peccoz, J. Larry Jameson, John C. Achermann, Gokhan Ozisik, Luca Persani, Anna Spada
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 88:417-423
Mutations in DAX1 [dosage-sensitive sex reversal-adrenal hypoplasia congenita (AHC) critical region on the X chromosome gene 1; NR0B1] cause X-linked AHC, a disease characterized by primary adrenal failure in infancy or childhood and reproductive abn
Publikováno v:
Hormone Research in Paediatrics. 59:94-98
SF1 (steroidogenic factor-1; NR5A1) is an orphan nuclear receptor that is expressed in the adrenal gland, gonads, spleen, ventromedial hypothalamus and pituitary gonadotroph cells. Combined approaches of targeted mutagenesis in mice and examination o
Autor:
Koray Harmanci, J. Larry Jameson, Berkan Gürakan, John C. Achermann, Utku Arman Örün, Masafumi Ito, Gokhan Ozisik
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:1829-1833
The orphan nuclear receptor steroidogenic factor-1 (SF-1, NR5A1) regulates the transcription of multiple genes involved in steroidogenesis, reproduction, and male sexual differentiation. A heterozygous loss-of-function SF-1 mutation (G35E) has been d
Autor:
Roberto Romoli, Luca Persani, John C. Achermann, Giorgio Borretta, Anna Spada, Paolo Beck-Peccoz, J. Larry Jameson, Giovanna Mantovani, Gokhan Ozisik
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:44-48
Mutations in the orphan nuclear receptor DAX-1 cause X-linked adrenal hypoplasia congenita. Affected boys usually present with primary adrenal failure in early infancy or childhood. Impaired sexual development because of hypogonadotropic hypogonadism
Autor:
Gokhan Ozisik, Sidika Ayse Ozer, Cenk Aral, Zebra Atabey, Sinan Caglayan, Metin Ozata, Filiz Ozdemir Sertoglu, Mustafa Akkiprik
Publikováno v:
Volume: 41, Issue: 3 533-541
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Acid phosphatase locus 1 (ACP1) encodes a polymorphic enzyme and has potential implications for the development of metabolic syndrome (MS) by altering insulin sensitivity. The aim of this study was to determine whether a relationship exists between A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93de423ac13ecb48873b6bc2831761ad
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12304/147264
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12304/147264
Publikováno v:
Journal of Endocrinological Investigation. 21:337-341
Leptin, the product of the adipose specific ob gene, regulates food intake and energy expenditure. However, little is known about the effects of thyroid status on plasma leptin levels in women. We determined fasting plasma leptin levels before and 1
Autor:
Gokhan Ozisik, Ayşe Özer, Cenk Aral, Nuray Bekiroglu, Sinan Caglayan, Zehra Atabey, Mustafa Akkiprik
Publikováno v:
Scopus-Elsevier
ResearcherID
ResearcherID
OBJECTIVE: Mitochondrial DNA (mtDNA) polymorphisms have been implicated in the pathophysiology of human diseases. Among them, a T>C nucleotide transition on the 16189 nucleotide position of mtDNA has been studied in several metabolic diseases includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::600513e720a83d63a234ce1734a5985c
https://hdl.handle.net/20.500.11776/6832
https://hdl.handle.net/20.500.11776/6832