Search Results - "Erdal, M E"

Effect of EGF on Bax, Bcl-2 and Fas expression in ulcerous disease and N87 cell line by Soylemez, F, Ay, O I, Ay, E, Altintas, E, Turkseven, C H, Erdal, M E

“…To evaluate the effect of epithelial growth factor (EGF) in primary culture of ulcer patients and N87 cell line on expressions of apoptotic genes. Ulcer…”
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The importance of IRS-1 Gly972Arg polymorphism in evaluating the response to metformin treatment in polycystic ovary syndrome by Ertunc, D., Tok, E.C., Aktas, A., Erdal, E.M., Dilek, S.

“…BACKGROUND: Recent evidence suggests that one of the modes of action of metformin may be through phosphorylation of the insulin receptor and insulin receptor…”
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T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction by Mutlu, N, Erdal, ME, Herken, H, Oz, G, Bayazıt, YA

“…Objective:  To assess whether a relationship existed between the T102C polymorphism of 5‐HT2A receptor gene and temporomandibular dysfunction. Methods: …”
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Microchimerism in vitiligo by Kurtulus, P.I., Tursen, U., Erdal, M.E.

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Relationship between the DAT1 gene and the effects of methylphenidate administration in adult attention deficit hyperactivity disorder: a magnetic resonance spectroscopy study by Inci Kenar, A N, Ünal, G A, Güler, H, Albuz, B, Kıroğlu, Y, Erdal, M E, Herken, H

“…This study investigated the relationship between DAT1 gene polymorphisms and the effects of methylphenidate (MPH) administration on N-acetyl aspartate (NAA),…”
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Is the dopamine D3 receptor mRNA on blood lymphocytes help to for identification and subtyping of schizophrenia? by Urhan-Kucuk, M., Erdal, M. E., Ozen, M. E., Kul, S., Herken, H.

“…Schizophrenia is one of the neuropathological disorders, which are associated with dopamine and its receptors. In recent years, it has been shown that mRNA of…”
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Evaluation of glucose metabolism and reproductive hormones in polycystic ovary syndrome on the basis of peroxisome proliferator-activated receptor (PPAR)-γ2 Pro12Ala genotype by Tok, E.C., Aktas, A., Ertunc, D., Erdal, E.M., Dilek, S.

“…BACKGROUND: Peroxisome proliferator-activated receptor (PPAR)-γ2 Pro12Ala polymorphism has been suggested as a protective factor for polycystic ovary syndrome…”
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Tumour necrosis factor alpha -308G/A gene polymorphism: lack of association with knee osteoarthritis in a Turkish population by Sezgin, M, Barlas, I O, Ankarali, H C, Altintaş, Z M, Türkmen, E, Gökdoğan, T, Sahin, G, Erdal, M E

“…To study the association between TNFalpha-308 G/A polymorphism and susceptibility to and severity of knee osteoarthritis in a Turkish population. Genomic DNA…”
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Catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association between symptomatology and prognosis by Herken, H, Erdal, M E

“…Catechol-O-methyltransferase (COMT) gene has long been implicated to play a role in the pathogenesis of schizophrenia. The aim of this study is to assess the…”
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Significance of serotonin transporter gene polymorphism in migraine by Yılmaz, Mustafa, Erdal, M.Emin, Herken, Hasan, Çataloluk, Osman, Barlas, Ömer, Bayazıt, Yıldırım A

“…Objective. To elucidate significance of the serotonin transporter gene (STG) polymorphism in migraine, and to address the polymorphic patterns of STG, both in…”
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Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine by Erdal, M.Emin, Herken, Hasan, Yılmaz, Mustafa, Bayazıt, Yıldırım A.

“…Objective: To find out the significance of the 5-HT2A receptor gene polymorphism in migraine. Study design: A PCR study in which 61 migraineurs and 44 healthy…”
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Tumour necrosis factor a -308G/A gene polymorphism : lack of association with knee osteoarthritis in a Turkish population by SEZGIN, M, BARLAS, I. O, ANKARALI, H. C, ALTINTAS, Z. M, TÜRKMEN, E, GÖKDOGAN, T, SAHIN, G, ERDAL, M. E

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Evaluation of glucose metabolism and reproductive hormones in polycystic ovary syndrome on the basis of peroxisome proliferator-activated receptor (PPAR)-gamma2 Pro12Ala genotype by Tok, E C, Aktas, A, Ertunc, D, Erdal, E M, Dilek, S

“…Peroxisome proliferator-activated receptor (PPAR)-gamma2 Pro12Ala polymorphism has been suggested as a protective factor for polycystic ovary syndrome (PCOS)…”
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Evaluation of glucose metabolism and reproductive hormones in polycystic ovary syndrome on the basis of peroxisome proliferator-activated receptor (PPAR)-[gamma]2 Pro12Ala genotype by Tok, E C, Aktas, A, Ertunc, D, Erdal, E M, Dilek, S

“…BACKGROUND: Peroxisome proliferator-activated receptor (PPAR)-γ2 Pro12Ala polymorphism has been suggested as a protective factor for polycystic ovary syndrome…”
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The impact of synapsin III gene on the neurometabolite level alterations after single-dose methylphenidate in attention-deficit hyperactivity disorder patients by Başay, Ömer, Kabukcu Basay, Burge, Alacam, Huseyin, Ozturk, Onder, Buber, Ahmet, Gorucu Yilmaz, Senay, Kıroğlu, Yılmaz, Erdal, Mehmet Emin, Herken, Hasan

“…To investigate the neurometabolite level changes according to synapsin III gene rs133945G>A and rs133946C>G polymorphisms by using magnetic resonance…”
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Serotonin transporter gene polymorphism in irritable bowel syndrome by Pata, Cengiz, Erdal, Emin M., Derici, Ebru, Yazar, Aziz, Kanık, Arzu, Ulu, Oğuz

“…Serotonin is a key mediator of intestinal peristalsis, and after it is secreted, it is effectively cleansed from the neuronal gap by means of a high affinity…”
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Microribonucleic acid dysregulations in children and adolescents with obsessive-compulsive disorder by Kandemir, Hasan, Erdal, Mehmet Emin, Selek, Salih, İzci Ay, Özlem, Karababa, İbrahim Fatih, Ay, Mustafa Ertan, Kandemir, Sultan Basmacı, Yılmaz, Şenay Görücü, Ekinci, Suat, Taşdelen, Bahar, Bayazit, Hüseyin

“…Obsessive-compulsive disorder (OCD) is a disorder characterized by the presence of obsessions and/or compulsions. Although disorder etiology and pathogenesis…”
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Association of Gly972Arg variant of insulin receptor substrate-1 with metabolic features in women with polycystic ovary syndrome by Dilek, Saffet, Ertunc, Devrim, Tok, Ekrem C, Erdal, Emin M, Aktas, Atil

“…To examine the prevalence and the effects of Gly972Arg (G972A) variant of insulin receptor substrate-1 (IRS-1) in women with polycystic ovary syndrome (PCOS)…”
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Extracellular Matrix Protein 1 Gene (ECM1) Mutations in Lipoid Proteinosis and Genotype-Phenotype Correlation by Hamada, Takahiro, Wessagowit, Vesarat, South, Andrew P., Ashton, Gabrielle H.S., Chan, Ien, Oyama, Noritaka, Siriwattana, Apatorn, Jewhasuchin, Prachiya, Charuwichitratana, Somyot, Thappa, Devinder M., Lenane, Patsy, Krafchik, Bernice, Kulthanan, Kanokvalai, Shimizu, Hiroshi, Kaya, Tamer I., Erdal, Mehmet E., Paradisi, Mauro, Paller, Amy S., Seishima, Mariko, Hashimoto, Takashi, McGrath, John A.

“…The autosomal recessive disorder lipoid proteinosis results from mutations in extracellular matrix protein 1 (ECM1), a glycoprotein expressed in several…”
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White matter alterations related to attention-deficit hyperactivity disorder and COMT val158met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus) by Herken, Hasan, Kabukçu Başay, Bürge, Büber, Ahmet, Başay, Ömer, Alacam, Hüseyin, Öztürk, Önder, Suren, Serkan, Izci Ay, Ozlem, Agladioglu, Kadir, Erdal, Mehmet Emin, Ercan, Eyup, Acikel, Cengizhan

“…Burge Kabukcu Basay,1 Ahmet Buber,1 Omer Basay,1 Huseyin Alacam,2 Onder Ozturk,1 Serkan Suren,3 Ozlem Izci Ay,4 Cengizhan Acikel,5 Kadir Agladioglu,6 Mehmet…”
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