Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 82 Records) |
Query Trace: SRY[original query] |
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Long Noncoding RNA SOX2-OT: Regulations, Functions, and Roles on Mental Illnesses, Cancers, and Diabetic Complications. BioMed research international 2020 12 2020 2901589. Li Pu-Yu, Wang Ping, Gao She-Gan, Dong Dao-Y |
SMARCA4/BRG1-Deficient Non-Small Cell Lung Carcinomas: A Case Series and Review of the Literature. Archives of pathology & laboratory medicine 2021 Jan 145 (1): 90-98. Nambirajan Aruna, Singh Varsha, Bhardwaj Nishu, Mittal Saurabh, Kumar Sunil, Jain Deepa |
Association of Exon 14 of the SOX6 Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia. Hemoglobin 2020 11 44 (6): 406-410. Mohammadi Zahra, Mohammadi Reza, Haghpanah Sezaneh, Moghadam Mohamad, Pazhoomand Reza, Karimi Mehr |
SOX13 gene downregulation in peripheral blood mononuclear cells of patients with Klinefelter syndrome. Asian journal of andrology 2020 10 23 (2): 157-162. Cannarella Rossella, Salemi Michele, Condorelli Rosita A, Cimino Laura, Giurato Giorgio, Marchese Giovanna, Cordella Angela, Romano Corrado, La Vignera Sandro, Calogero Aldo |
Pleiotropic Locus 15q24.1 Reveals a Gender-Specific Association with Neovascular but Not Atrophic Age-Related Macular Degeneration (AMD). Cells 2020 10 9 (10): . Kiel Christina, Strunz Tobias, International Amd Genomics Consortium Project Manager Susan Blanton Iamdgc , Grassmann Felix, Weber Bernhard H |
Prevalence of Y chromosome microdeletion in azoospermia factor subregions among infertile men from West Bengal, India. Molecular genetics & genomic medicine 2021 Aug e1769. Dutta Saurav, Paladhi Pranab, Pal Samudra, Bose Gunja, Ghosh Papiya, Chattopadhyay Ratna, Chakravarty Baidyanath, Ghosh Suj |
Molecular study and genotype-phenotype in Chinese female patients with 46, XY disorders of sex development. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2021 8 37 (10): 934-940. Xia Junke, Wu Jing, Chen Chen, Zhao Zhenhua, Xie Yanchuan, Bai Zhouxian, Kong Xiangdo |
The effect of SOX4 gene 3'UTR polymorphisms on osteoporosis. Journal of orthopaedic surgery and research 2021 May 16 (1): 321. Li Guo, Gu Zuchao, He Yue, Wang Chongwen, Duan JiQia |
Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experience. Blood transfusion = Trasfusione del sangue 2021 4 20 (3): 235-244. Parchure Disha, Madkaikar Manisha, Kulkarni Swa |
Deletions on Chromosome Y and Downregulation of the SRY Gene in Tumor Tissue Are Associated with Worse Survival of Glioblastoma Patients. Cancers 2021 Mar 13 (7): . ?ysiak Ma?gorzata, Smits Anja, Roodakker Kenney Roy, Sandberg Elisabeth, Dimberg Anna, Mudaisi Munila, Bratthäll Charlotte, Strandeus Michael, Milos Peter, Hallbeck Martin, Söderkvist Peter, Malmström Anni |
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 2021 3 185 (6): 1666-1677. Mazen Inas, Mekkawy Mona, Kamel Alaa, Essawi Mona, Hassan Heba, Abdel-Hamid Mohamed, Amr Khalda, Soliman Hala, El-Ruby Mona, Torky Ahmed, El Gammal Mona, Elaidy Aya, Bashamboo Anu, McElreavey Kenne |
Clinical and Genetic Characteristics of 17 ?-Hydroxylase/17, 20-Lyase Deficiency: c.985_987delTACinsAA Mutation of CYP17A1 Prevalent in the Chinese Han Population. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 Dec . Xia Junke, Liu Furong, Wu Jing, Xia Yanjie, Zhao Zhenhua, Zhao Yongjiang, Ren Huayan, Kong Xiangdo |
Copy number variation of the SRY gene showed an association with disorders of sex development in Yorkshire Terrier dogs. Animal genetics 2021 10 53 (1): 152-155. Krzeminska P, Nowacka-Woszuk J, Switonski |
A large cohort of disorders of sex development and their genetic characteristics: 6 novel mutations in known genes. European journal of medical genetics 2021 1 64 (3): 104154. Ata Aysun, Özen Samim, Onay Hüseyin, Uzun Selin, Gök?en Damla, Özk?nay Ferda, Özbaran Nazl? Burcu, Ulman ?brahim, Darcan ?ükr |
Clinical implications and genetical insights of SOX6 expression in acute myeloid leukemia. Journal of cancer research and clinical oncology 2022 9 . Li Yan, Jiang Duanfeng, Zhang Qin, Liu Enyi, Shao Haiga |
Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature. Andrology 2022 Aug . Capron Céline, Januel Louis, Vieville Gaëlle, Jaillard Sylvie, Kuentz Paul, Salaun Gaëlle, Nadeau Gwenaël, Clement Patrice, Brechard Marie Pierre, Herve Bérénice, Dupont Jean Michel, Gruchy Nicolas, Chambon Pascal, Abdelhedi Fatma, Dahlen Eric, Vago Philippe, Harbuz Radu, Plotton Ingrid, Coutton Charles, Belaud-Rotureau Marc-Antoine, Schluth-Bolard Caroline, Vialard Franço |
Mutation analysis of circulating tumor DNA and paired ascites and tumor tissues in ovarian cancer. Experimental and therapeutic medicine 2022 8 24 (3): 542. Jie Xiaoxiang, Du Ming, Zhang Meng, Jin Xiayu, Cai Qingqing, Xu Congjian, Zhang Xiaoy |
Mixed model-based eQTL analysis reveals lncRNAs associated with regulation of genes involved in sex determination and spermatogenesis: The key to understanding human gender imbalance. Computational biology and chemistry 2022 6 99 107713. An Yeeun, Lee Chaeyou |
Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs. Genomics 2022 5 114 (4): 110389. Nowacka-Woszuk Joanna, Stachowiak Monika, Szczerbal Izabela, Szydlowski Maciej, Szabelska-Beresewicz Alicja, Zyprych-Walczak Joanna, Krzeminska Paulina, Nowak Tomasz, Lukomska Anna, Ligocka Zuzanna, Biezynski Janusz, Dzimira Stanislaw, Nizanski Wojciech, Switonski Mar |
RHD exon 5, 7 and 10 targeted non-invasive prenatal screening of fetal Rhesus-D (RhD) in selected RhD negative pregnant women in Ethiopia. PloS one 2022 3 17 (3): e0265583. Niguse Birhanu, Ermias Mihertab, Berhanu Solomon, Abayneh Lemma, Chakiso Bekele, Rather Riyaz Ahm |
SRY and NR5A1 gene mutation in Algerian children and adolescents with DSD and testicular dysgenesis. African health sciences 2021 Sep 21 (3): 1491-1497. Kherouatou-Chaoui Naouel, Chellat-Rezgoune Djalila, Rezgoune Mohamed Larbi, Mc Elreavey Ken, Touabti Laaldja Souhem, Abadi Noreddine, Satta Dali |
Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene. Molecular cytogenetics 2022 2 15 (1): 2. Qin Shengfang, Wang Xueyan, Wang J |
Cytogenetic and molecular insight into the genetic background of disorders of sex development in seventeen cats. Scientific reports 2022 10 12 (1): 17807. Stachowiak Monika, Szczerbal Izabela, Nowacka-Woszuk Joanna, Nowak Tomasz, Sowinska Natalia, Lukomska Anna, Gogulski Maciej, Badura Malgorzata, Sklorz-Mencel Karolina, Jagodka Dariusz, Nizanski Wojciech, Dzimira Stanislaw, Switonski Mar |
Shared genetic liability between major depressive disorder and osteoarthritis. Bone & joint research 2022 1 11 (1): 12-22. Zhang Fuquan, Rao Shuquan, Baranova Anc |
rs66651343 and rs12909095 confer lung cancer risk by regulating CCNDBP1 expression. PloS one 2023 4 18 (4): e0284347. Shi Qiang, Ruan Ji, Yang Yu-Chen, Shi Xiao-Qian, Liu Shao-Dong, Wang Hong-Yan, Zhang Shi-Jiao, Wang Si-Qi, Zhong Li, Sun Cha |
SMARCA4?deficient non?small cell lung cancer with an EGFR mutation: A case report. Oncology letters 2023 11 26 (6): 513. Lijun Sun, Qiong Fu, Lijiang Chen, Meijuan Di, Jianhua C |
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development. Molecular human reproduction 2023 1 29 (2): . Kulkarni Vinayak, Chellasamy Selvaa Kumar, Dhangar Somprakash, Ghatanatti Jagdeeshwar, Vundinti Babu R |
Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development. Reproductive biology and endocrinology : RB&E 2023 1 21 (1): 2. Rjiba Khouloud, Mougou-Zerelli Soumaya, Hamida Imen Hadj, Saad Ghada, Khadija Bochra, Jelloul Afef, Slimani Wafa, Hasni Yosra, Dimassi Sarra, Khelifa Hela Ben, Sallem Amira, Kammoun Molka, Abdallah Hamza Hadj, Gribaa Moez, Bignon-Topalovic Joelle, Chelly Sami, Khairi Hédi, Bibi Mohamed, Kacem Maha, Saad Ali, Bashamboo Anu, McElreavey Kenne |
SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians. European journal of medical research 2024 1 29 (1): 66. Hemender Singh, Shipra, Manish Gupta, Nital Gupta, Geetanjali Gupta, Ajay K Pandita, Rajesh Sharma, Sarla Pandita, Vinod Singh, Bhavuk Garg, Ekta Rai, Swarkar Shar |
Association of SOX6 gene polymorphisms with Kashin-Beck disease risk in the Chinese Han population. Open medicine (Warsaw, Poland) 2024 1 19 (1): 20230883. Na He, Aiwen Hong, Kun Zhao, Zhefan Zhang, Shengli Wang, Yaofei J |
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- Page last updated:Apr 22, 2024
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