Search Results - "ARSEVEN, O"

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  1. 1

    The frequency of deep venous thrombosis and pulmonary embolus in acute exacerbation of chronic obstructive pulmonary disease by ERELEL, M., ÇUHADARO Ǧ, Ç., ECE, T., ARSEVEN, O.

    Published in Respiratory medicine (01-07-2002)
    “…Infection, pulmonary embolism caused by mostly deep venous thrombosis (DVT), hypoxaemia and drugs, used in the treatment of chronic obstructive pulmonary…”
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    Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene by KOPP, P, ARSEVEN, O. K, SABACAN, L, KOTLAR, T, DUPUIS, J, CAVALIERE, H, SANTOS, C. L. S, JAMESON, J. L, MEDEIROS-NETO, G

    “…Pendred's syndrome is an autosomal recessive disease characterized by goiter, impaired iodide organification, and congenital sensorineural deafness. The gene…”
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  3. 3

    Clinical and molecular analysis of three Mexican families with Pendred's syndrome by GONZALEZ TREVINO, O, KARAMANOGLU ARSEVEN, O, CEBALLOS, C. J, VIVES, V. I, RAMIREZ, R. C, GOMEZ, V. V, MEDEIROS-NETO, G, KOPP, P

    Published in European journal of endocrinology (01-06-2001)
    “…The autosomal recessive Pendred's syndrome is defined by congenital sensorineural deafness, goiter, and impaired iodide organification. It is caused by…”
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    Evaluation of undergraduate training on tuberculosis at Istanbul Medical School by KILICASLAN, Z, KIYAN, E, ERKAN, F, GURGAN, M, AYDEMIR, N, ARSEVEN, O

    “…SETTING: Undergraduate training on tuberculosis at Istanbul Medical School.OBJECTIVE: To assess whether tuberculosis-related questions asked in chest medicine…”
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    Impact of Promising Biomarkers on Severity and Outcome of Acute Pulmonary Embolism by Sagcan, Gulseren, Dogan, Zeki, Uzun, Hafize, Cuhadaroglu, Caglar, Okumus, Gulfer, Arseven, Orhan

    Published in International journal of general medicine (31-08-2023)
    “…Acute pulmonary embolism (APE) is a common clinical condition. Its severity ranges from asymptomatic radiological findings to fatal obstructive shock. The…”
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    Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil by Nogueira, C R, Kopp, P, Arseven, O K, Santos, C L, Jameson, J L, Medeiros-Neto, G

    Published in Thyroid (New York, N.Y.) (01-11-1999)
    “…Constitutively activating mutations in the thyrotropin (TSH) receptor have been identified as a major molecular cause of hyperfunctioning thyroid adenomas. A…”
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    Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia by Nogueira, C R, Nguyen, L Q, Coelho-Neto, J R, Arseven, O K, Jameson, J L, Kopp, P, Medeiros-Neto, G A

    Published in Thyroid (New York, N.Y.) (01-06-1999)
    “…Sporadic congenital hypothyroidism is most commonly caused by developmental abnormalities of the thyroid gland. More rarely, it is due to defects in gene…”
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    Bilateral facial paralysis secondary to lymphoma by Ozmenoğlu, M, Arseven, O, Candan, S, Siviloğlu, C

    “…We report a patient with bilateral facial palsy due to a non-Hodgkin lymphoma. He was initially diagnosed to have a facial paralysis of unknown aetiology…”
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    Substitutions of tyrosine 601 in the human thyrotropin receptor result in increase or loss of basal activation of the cyclic adenosine monophosphate pathway and disrupt coupling to Gq/11 by Arseven, O K, Wilkes, W P, Jameson, J L, Kopp, P

    Published in Thyroid (New York, N.Y.) (01-01-2000)
    “…Constitutively activating mutations of the thyrotropin (TSH) receptor have been identified as a molecular cause of toxic adenomas, nonautoimmune familial…”
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  14. 14

    The thyroid hormone receptor variant alpha2 is a weak antagonist because it is deficient in interactions with nuclear receptor corepressors by Tagami, T, Kopp, P, Johnson, W, Arseven, O K, Jameson, J L

    Published in Endocrinology (Philadelphia) (01-05-1998)
    “…The thyroid hormone receptor splice variant, alpha2, is unable to bind thyroid hormone (T3) and has been proposed to function as an endogenous inhibitor of T3…”
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  15. 15

    Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1 by Kopp, P., Arseven, O. Karamanoglu, Sabacan, L., Kotlar, T., Dupuis, J., Cavaliere, H., Santos, C. L. S., Jameson, J. L., Medeiros-Neto, G.

    “…Pendred’s syndrome is an autosomal recessive disease characterized by goiter, impaired iodide organification, and congenital sensorineural deafness. The gene…”
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    Proteolysis of the Mismatch Repair Protein MLH1 by Caspase-3 Promotes DNA Damage-induced Apoptosis by Chen, Feng, Arseven, Onur K., Cryns, Vincent L.

    Published in The Journal of biological chemistry (25-06-2004)
    “…Caspases are critical proapoptotic proteases that execute cell death signals by selectively cleaving proteins at Asp residues to alter their function. Caspases…”
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    Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism by Nguyen, Lynda Q, Arseven, Onur Karamanoglu, Gerber, Hans, Stein, Barbara S, Jameson, J Larry, Kopp, Peter

    Published in Endocrinology (Philadelphia) (01-02-2002)
    “…Cats are the only nonhuman mammalian species with a high incidence of hyperthyroidism, and a better understanding of the pathogenesis of feline hyperthyroidism…”
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    Exogenous allergic alveolitis caused by mouldy hazel nut leaves by Erkan, F, Baur, X, Kiliçaslan, Z, Tabak, L, Arseven, O, Erelel, M, Jaeger, D, Cavdar, T

    Published in Pneumologie (Stuttgart, Germany) (01-01-1992)
    “…A 62-year old farmer woman from the northeastern, very rainy part of Turkey has been collecting large amounts of green and brown involucral hazel-nut leaves…”
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