المؤلفون: Aleksandra Maria Roztoczyńska, Dorota Roztoczyńska, Antoni Pyrkosz, Artur Mazur

المصدر: Pediatria Polska, Vol 99, Iss 1, Pp 94-98 (2024)

مصطلحات موضوعية: setd5, short stature, specific dysmorphia features., Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: https://www.termedia.plTest/SETD5-gene-mutation-as-the-cause-of-short-stature,127,52488,1,1.html; https://doaj.org/toc/0031-3939Test; https://doaj.org/toc/2300-8660Test

الوصول الحر: https://doaj.org/article/3c4aef2f93424d63b65260548187ae77Test

المؤلفون: Mehdi Hashemipour, Motahareh Sheikh-Hosseini, Hadideh Mabudi

المصدر: International Journal of Biomedicine, Vol 14, Iss 1, Pp 170-174 (2024)

مصطلحات موضوعية: autism spectrum disorder, setd5 gene, mutation, Medicine

وصف الملف: electronic resource

العلاقة: http://www.ijbm.org/articles/i53/ijbm_14Test(1)_cr4.pdf; https://doaj.org/toc/2158-0510Test; https://doaj.org/toc/2158-0529Test

الوصول الحر: https://doaj.org/article/52032793fa944b49aa54b423ae2a88e6Test

المؤلفون: Mingyang Li, Yanan Hou, Ziwei Zhang, Bowen Zhang, Ting Huang, Aiqin Sun, Genbao Shao, Qiong Lin

المصدر: Frontiers in Endocrinology, Vol 14 (2023)

مصطلحات موضوعية: SETD5, lysine methyltransferase, posttranslational modifications, methylation, neurodevelopmental disorder (NDD), cancer, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fendo.2023.1089527/fullTest; https://doaj.org/toc/1664-2392Test

الوصول الحر: https://doaj.org/article/21c7a2e754914f68afcad7a03a04addbTest

المؤلفون: Tadashi Nakagawa, Satoko Hattori, Toru Hosoi, Keiko Nakayama

المصدر: Frontiers in Genetics, Vol 13 (2023)

مصطلحات موضوعية: SETD5, IDD23, ANKRD11, KBG syndrome, mouse model, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2022.1022339/fullTest; https://doaj.org/toc/1664-8021Test

الوصول الحر: https://doaj.org/article/220e7714b9a447b5a624ba44132757deTest

المؤلفون: Chiara Gabellini, Cecilia Pucci, Chiara De Cesari, Davide Martini, Caterina Di Lauro, Matteo Digregorio, William Norton, Alessio Zippo, Alessandro Sessa, Vania Broccoli, Massimiliano Andreazzoli

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 1, p 167 (2022)

مصطلحات موضوعية: setd5, zebrafish, autism, neurodevelopment, behavior, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1422-0067/24/1/167Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test

الوصول الحر: https://doaj.org/article/5a080da48fef40eb870b24c29032352eTest

المؤلفون: Gabellini, Chiara, Pucci, Cecilia, De Cesari, Chiara, Martini, Davide, Di Lauro, Caterina, Digregorio, Matteo, Norton, William, Zippo, Alessio, Sessa, Alessandro, Broccoli, Vania, Andreazzoli, Massimiliano

المساهمون: Gabellini, Chiara, Pucci, Cecilia, De Cesari, Chiara, Martini, Davide, Di Lauro, Caterina, Digregorio, Matteo, Norton, William, Zippo, Alessio, Sessa, Alessandro, Broccoli, Vania, Andreazzoli, Massimiliano

مصطلحات موضوعية: setd5, zebrafish, autism, neurodevelopment, behavior

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000910157100001; volume:24; issue:1; firstpage:167; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/11568/1161344Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85145998077; https://www.mdpi.com/1422-0067/24/1/167Test

الإتاحة: https://doi.org/10.3390/ijms24010167Test
https://hdl.handle.net/11568/1161344Test
https://www.mdpi.com/1422-0067/24/1/167Test

المؤلفون: Lavínia Mota de Miranda, Eduarda, Karoline Lacerda Sousa Silva, Ana, Paula Vasconcelos Páuda, Ana, Emanuele Pereira Domingues, Fernanda, Orlandi Rosa, Letícia, Marques Araújo, Francielle, Thalita dos Reis, Sabrina

المصدر: Health and Society; Vol. 2 No. 01 (2022) ; Health and Society; v. 2 n. 01 (2022) ; 2763-5724 ; 10.51249/hs.v2i01

مصطلحات موضوعية: setd5, shank3, autism, prognosis

وصف الملف: application/pdf

العلاقة: https://www.periodicojs.com.br/index.php/hs/article/view/663/520Test; https://www.periodicojs.com.br/index.php/hs/article/view/663Test

الإتاحة: https://doi.org/10.51249/hs.v2i01.663Test
https://doi.org/10.51249/hs.v2i01Test
https://www.periodicojs.com.br/index.php/hs/article/view/663Test

المؤلفون: Francesca Cogliati, Francesca Forzano, Silvia Russo

المصدر: Frontiers in Neurology, Vol 12 (2021)

مصطلحات موضوعية: overlapping phenotypes, pleiotropy of a single gene, microcephaly, SETBP1 gene, SETD5 gene, MRD23 syndrome, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2021.711288/fullTest; https://doaj.org/toc/1664-2295Test

الوصول الحر: https://doaj.org/article/96c789c819cc4c6c8d0acb91f3713e6aTest

المؤلفون: Hairu Yu, Jiayi Sun, Congxuan Zhao, Haotian Wang, Yeqiu Liu, Jiajia Xiong, Jing Chang, Mixue Wang, Wenhui Wang, Dongman Ye, Hongyan Zhou, Tao Yu

المصدر: BMC Cancer, Vol 19, Iss 1, Pp 1-10 (2019)

مصطلحات موضوعية: SET domain containing 5 (SETD5), Non-small cell lung cancer, Invasion, ERK signaling, Prognosis, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12885-019-5944-2Test; https://doaj.org/toc/1471-2407Test

الوصول الحر: https://doaj.org/article/32550c4e0f594b7e82bdbbf1a8adab63Test

المؤلفون: Milena Crippa, Ilaria Bestetti, Silvia Maitz, Karin Weiss, Alice Spano, Maura Masciadri, Sarah Smithson, Lidia Larizza, Karen Low, Lior Cohen, Palma Finelli

المصدر: Frontiers in Neurology, Vol 11 (2020)

مصطلحات موضوعية: MRD23, 3p25 microdeletion syndrome, KBG syndrome, SETD5 haploinsufficiency, WES, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fneur.2020.00631/fullTest; https://doaj.org/toc/1664-2295Test

الوصول الحر: https://doaj.org/article/0ef7aae585f645aa881ecd90a799dbc0Test