Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Cangul, Hakan"'
Publikováno v:
Environmental Health Perspectives, 2002 Oct 01. 110, 783-788.
Externí odkaz:
https://www.jstor.org/stable/3455092
Publikováno v:
Philosophical Transactions: Biological Sciences, 2015 Feb 01. 370(1661), 1-9.
Externí odkaz:
http://www.jstor.org/stable/24504255
Akademický článek
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Autor:
Cangul, Hakan, Liao, Xiao-Hui, Schoenmakers, Erik, Kero, Jukka, Barone, Sharon, Srichomkwun, Panudda, Iwayama, Hideyuki, Serra, Eva G, Saglam, Halil, Eren, Erdal, Tarim, Omer, Nicholas, Adeline K, Zvetkova, Ilona, Anderson, Carl A, Frankl, Fiona E Karet, Boelaert, Kristien, Ojaniemi, Marja, Jääskeläinen, Jarmo, Patyra, Konrad, Löf, Christoffer, Williams, E Dillwyn, UK10K Consortium, Soleimani, Manoocher, Barrett, Timothy, Maher, Eamonn R, Chatterjee, V Krishna, Refetoff, Samuel, Schoenmakers, Nadia
WOS: 000447709700003 PubMed ID: 30333321 Defects in genes mediating thyroid hormone biosynthesis result in dyshormonogenic congenital hypothyroidism (CH). Here, we report homozygous truncating mutations in SLC26A7 in 6 unrelated families with goitrou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a381f4f99fc2b08947d30a8c589dd941
https://hdl.handle.net/20.500.12511/2911
https://hdl.handle.net/20.500.12511/2911
Autor:
Cangul, Hakan1 (AUTHOR) h.cangul@bham.ac.uk, Darendeliler, Feyza2 (AUTHOR), Saglam, Yaman3 (AUTHOR), Kucukemre, Banu2 (AUTHOR), Kendall, Michaela4 (AUTHOR), Boelaert, Kristien5 (AUTHOR), Barrett, Timothy G.5 (AUTHOR), Maher, Eamonn R.6 (AUTHOR)
Publikováno v:
Endocrine Research. Aug2015, Vol. 40 Issue 3, p146-150. 5p. 3 Diagrams, 1 Chart.
Autor:
Cangul Hakan
Publikováno v:
BMC Genetics, Vol 5, Iss 1, p 27 (2004)
Abstract Background The expression of NDRG1 gene is induced by nickel, a transition metal sharing similar physical properties to cobalt. Nickel may create hypoxia-like conditions in cells and induce hypoxia-responsive genes, as does cobalt. Therefore
Externí odkaz:
https://doaj.org/article/7f4ef921bccc4993aec7ef8874ccca9e
Autor:
Nicholas, Adeline K, Serra, Eva G, Cangul, Hakan, Alyaarubi, Saif, Ullah, Irfan, Schoenmakers, Erik, Deeb, Asma, Habeb, Abdelhadi M, Almaghamsi, Mohammad, Peters, Catherine, Nathwani, Nisha, Aycan, Zehra, Saglam, Halil, Bober, Ece, Dattani, Mehul, Shenoy, Savitha, Murray, Philip G, Babiker, Amir, Willemsen, Ruben, Thankamony, Ajay, Lyons, Greta, Irwin, Rachael, Padidela, Raja, Tharian, Kavitha, Davies, Justin H, Puthi, Vijith, Park, Soo-Mi, Massoud, Ahmed F, Gregory, John W, Albanese, Assunta, Pease-Gevers, Evelien, Martin, Howard, Brugger, Kim, Maher, Eamonn R, Chatterjee, V Krishna K, Anderson, Carl A, Schoenmakers, Nadia
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Nicholas, A K, Serra, E G, Cangul, H, Alyaarubi, S, Ullah, I, Schoenmakers, E, Deeb, A, Habeb, A M, Almaghamsi, M, Peters, C, Nathwani, N, Aycan, Z, Saglam, H, Bober, E, Dattani, M, Shenoy, S, Murray, P G, Babiker, A, Willemsen, R, Thankamony, A, Lyons, G, Irwin, R, Padidela, R, Tharian, K, Davies, J H, Puthi, V, Park, S-M, Massoud, A F, Gregory, J W, Albanese, A, Pease-Gevers, E, Martin, H, Brugger, K, Maher, E R, Chatterjee, V K K, Anderson, C A & Schoenmakers, N 2016, ' Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ ', The Journal of Clinical Endocrinology and Metabolism, vol. 101, no. 12, pp. 4521-4531 . https://doi.org/10.1210/jc.2016-1879
Nicholas, A K, Serra, E G, Cangul, H, Alyaarubi, S, Ullah, I, Schoenmakers, E, Deeb, A, Habeb, A M, Almaghamsi, M, Peters, C, Nathwani, N, Aycan, Z, Saglam, H, Bober, E, Dattani, M, Shenoy, S, Murray, P G, Babiker, A, Willemsen, R, Thankamony, A, Lyons, G, Irwin, R, Padidela, R, Tharian, K, Davies, J H, Puthi, V, Park, S-M, Massoud, A F, Gregory, J W, Albanese, A, Pease-Gevers, E, Martin, H, Brugger, K, Maher, E R, Chatterjee, V K K, Anderson, C A & Schoenmakers, N 2016, ' Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ ', The Journal of Clinical Endocrinology and Metabolism, vol. 101, no. 12, pp. 4521-4531 . https://doi.org/10.1210/jc.2016-1879
Context: Lower TSH screening cutoffs have doubled the ascertainment of congenital hypothyroidism (CH), particularly cases with a eutopically located gland-in-situ (GIS). Although mutations in known dyshormonogenesis genes or TSHR underlie some cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0db38b423aebd37dd442bfb2eec37222
https://avesis.deu.edu.tr/publication/details/a9be71ee-4f58-47c1-9dfb-ba7f09647e55/oai
https://avesis.deu.edu.tr/publication/details/a9be71ee-4f58-47c1-9dfb-ba7f09647e55/oai
Akademický článek
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Akademický článek
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Autor:
Meyer, Esther, Pasha, Shanaz, Kirby, Gail A., Kendall, Michaela, Barrett, Timothy G., Yuca, Sevil A., Tarim, Omer, BÖBER, ECE, Cesur, Yasar, Maher, Eamonn R., Karkucak, Mutlu, Cetinkaya, Semra, Forman, Julia R., Eren, Erdal, Hogler, Wolfgang, YAKUT, TAHSİN, Aycan, Zehra, Cangul, Hakan, Gulten, Tuna, DEMİR, KORCAN, Saglam, Halil, Morgan, Neil V., Bas, Veysel
Nonsyndromic autosomal recessively inherited nongoitrous congenital hypothyroidism (CHNG) can be caused by mutations in TSHR, PAX8, TSHB and NKX2-5. We aimed to investigate mutational frequencies of these genes and genotype/phenotype correlations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::64f87c63afcb9abaf440b350cda24390
https://avesis.deu.edu.tr/publication/details/cac19f94-792e-418a-b543-fde9109bfcf1/oai
https://avesis.deu.edu.tr/publication/details/cac19f94-792e-418a-b543-fde9109bfcf1/oai