Zobrazeno 1 - 10
of 42
pro vyhledávání: '"CDC73 gene"'
Autor:
Yian Gu, Yuanyuan Ye, Hua Shu, Lina Chang, Yinghui Xie, Fengao Li, Tiehong Zhu, Ming Liu, Qing He
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundHereditary primary hyperparathyroidism (PHPT) accounts for 5-10% of all PHPT cases, necessitating genetic testing for diagnosis and management. Among these, hyperparathyroidism-jaw tumor syndrome (HPT-JT) is an autosomal dominant disorder c
Externí odkaz:
https://doaj.org/article/6b84efcc26fd47e88c8d66ed203a9ab1
Autor:
Francesca Marini, Francesca Giusti, Gaia Palmini, Cinzia Aurilia, Simone Donati, Maria Luisa Brandi
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 205-235 (2023)
Parathyroid carcinoma (PC) is a very rare endocrine cancer with aggressive behavior, a high metastatic potential, and a poor prognosis. Surgical resection of affected gland(s) and other involved structures is the elective therapy. Pre-operative and i
Externí odkaz:
https://doaj.org/article/a5f57f072a1e412ca4c6488930a3af7d
Autor:
Abdelmoneim Abdelrahman H., Mohammed Alaa I., Gadim Esraa O., Mohammed Mayada Alhibir, Hamza Sara H., Mirghani Sara A., Mahmoud Thwayba A., Hassan Mohamed A.
Publikováno v:
The EuroBiotech Journal, Vol 4, Iss 2, Pp 67-81 (2020)
Hyperparathyroidism-Jaw Tumor (HPT-JT) is an autosomal dominant disorder with variable expression, with an estimated prevalence of 6.7 per 1,000 population. Genetic testing for predisposing CDC73 (HRPT2) mutations has been an important clinical advan
Externí odkaz:
https://doaj.org/article/fcf6cf895d6a4644801d6931762e2a2e
Akademický článek
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Akademický článek
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Autor:
Mohamed Hassan, Thwayba A. Mahmoud, Sara A. Mirghani, Abdelrahman H. Abdelmoneim, Alaa I. Mohammed, Esraa O. Gadim, Sara H. Hamza, Mayada A. Mohammed
Publikováno v:
The EuroBiotech Journal, Vol 4, Iss 2, Pp 67-81 (2020)
Hyperparathyroidism-Jaw Tumor (HPT-JT) is an autosomal dominant disorder with variable expression, with an estimated prevalence of 6.7 per 1,000 population. Genetic testing for predisposing CDC73 (HRPT2) mutations has been an important clinical advan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a62c46ad4e385bf6d823b1339d9397b
https://doi.org/10.2478/ebtj-2020-0008
https://doi.org/10.2478/ebtj-2020-0008
Autor:
Rodrigo, Juan P., Hernandez-Prera, Juan C., Randolph, Gregory W., Zafereo, Mark E., Hartl, Dana M., Silver, Carl E, Suárez, Carlos, Owen, Randall P., Bradford, Carol R., Mäkitie, Antti A., Shaha, Ashok R., Bishop, Justin A., Rinaldo, Alessandra, Ferlito, Alfio
Parathyroid cancer (PC) is a rare malignant tumor which comprises 0.5-5% of patients with primary hyperparathyroidism (PHPT). Most of these cancers are sporadic, although it may also occur as a feature of various genetic syndromes including hyperpara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1593::b7eeeaaa4be6cc5084998c04999b2327
http://hdl.handle.net/10138/328203
http://hdl.handle.net/10138/328203
Akademický článek
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Autor:
Luisella Cianferotti, Ettore Luzi, Francesca Giusti, Roberto Zonefrati, Giorgio Gronchi, Simone Ciuffi, Maria Luisa Brandi, Francesca Marini, Giuliano Perigli, Gabriella Nesi
Hyperparathyrodism-jaw tumor (HPT-JT) syndrome is an autosomal dominant disorder. Loss of function of the cell division cycle protein 73 homolog (CDC73) gene is responsible for the syndrome. This gene encodes an ubiquitously expressed 531 amino acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67017d3743ea4cbdb7bdd13ae002dcb
http://hdl.handle.net/2158/1151329
http://hdl.handle.net/2158/1151329
Autor:
Rather, Mohammad Iqbal
CDC73, also known as HRPT2, is a tumour suppressor gene whose expression is lost or downregulated in parathyroid, renal, breast, uterine and gastric cancers. However, the reports regarding the role of CDC73 in oral squamous cell carcinoma (OSCC) are
Externí odkaz:
http://etd.iisc.ernet.in/2005/3414
http://etd.iisc.ernet.in/abstracts/4281/G25917-Abs.pdf
http://etd.iisc.ernet.in/abstracts/4281/G25917-Abs.pdf