Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 47 Records) |
Query Trace: C6[original query] |
---|
Frequent frameshift mutations in 2 mononucleotide repeats of RNF43 gene and its regional heterogeneity in gastric and colorectal cancers. Human pathology 2015 Jul . Jo Yun Sol, Kim Min Sung, Lee Ju Hwa, Lee Sug Hyung, An Chang Hyeok, Yoo Nam J |
Eye tracking indices of attentional bias in children of depressed mothers: Polygenic influences help to clarify previous mixed findings. Development and psychopathology 2015 Jun 1-13. Owens Max, Harrison Ashley J, Burkhouse Katie L, McGeary John E, Knopik Valerie S, Palmer Rohan H C, Gibb Brandon |
Predicting childhood effortful control from interactions between early parenting quality and children's dopamine transporter gene haplotypes. Development and psychopathology 2015 Apr 1-14. Li Yi, Sulik Michael J, Eisenberg Nancy, Spinrad Tracy L, Lemery-Chalfant Kathryn, Stover Daryn A, Verrelli Brian |
Association of novel SNPs in the candidate genes affecting caprine milk fatty acids related to human health. Meta gene 2015 Jun 4 45-56. Dixit S P, Sivalingam Jayakumar, Tyagi A K, Saroha V, Sharma A, Nagda R |
Polymorphisms in complement genes and risk of preeclampsia in Taiyuan, China. Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2016 Oct 65 (10): 837-45. Wu Weiwei, Yang Hailan, Feng Yongliang, Zhang Ping, Li Shuzhen, Wang Xin, Peng Tingting, Wang Fang, Xie Bingjie, Guo Pengge, Li Mei, Wang Ying, Zhao Nan, Wang Dennis, Wang Suping, Zhang Yaw |
Recipient C6 rs9200 genotype is associated with hepatocellular carcinoma recurrence after orthotopic liver transplantation in a Han Chinese population. Cancer gene therapy 2016 May . Wang Z, Liao J, Wu S, Li C, Fan J, Peng |
Association between the expression levels of TAZ, AXL and CTGF and clinicopathological parameters in patients with colon cancer. Oncology letters 2016 Feb 11 (2): 1223-1229. Zhang Shu-Dong, McCrudden Cian M, Yuen Hiu-Fung, Leung Ka Lai, Hong Wan-Jin, Kwok Hang F |
Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population.
Molecular medicine reports 2016 Dec . Baek Seung-Hoon, Kim Kang-Il, Yoon Kyung-Sik, Kim Tae-Ho, Kim Shin-Yo |
Dopamine receptor D2 (DRD2), dopamine transporter solute carrier family C6, member 4 (SLC6A3), and catechol-O-methyltransferase (COMT) genes as moderators of the relation between maternal history of maltreatment and infant emotion regulation. Development and psychopathology 2017 8 30 (2): 581-592. Villani Vanessa, Ludmer Jaclyn, Gonzalez Andrea, Levitan Robert, Kennedy James, Masellis Mario, Basile Vincenzo S, Wekerle Christine, Atkinson Lesl |
Gene Variations of Sixth Complement Component Affecting Tacrolimus Metabolism in Patients with Liver Transplantation for Hepatocellular Carcinoma. Chinese medical journal 2017 Jul 130 (14): 1670-1676. Liao Jian-Hua, Li Chang-Can, Wu Shao-Han, Fan Jun-Wei, Gu Hai-Tao, Wang Zhao-W |
Genetic predisposition for chronic venous insufficiency in several genes for matrix metalloproteinases (MMP-2, MMP-9, MMP-12) and their inhibitor TIMP-2. Journal of the European Academy of Dermatology and Venereology : JEADV 2017 Jun . Slonková V, Slonková V, Vašk? A, Vašk? |
Cumulative prenatal exposure to adversity reveals associations with a broad range of neurodevelopmental outcomes that are moderated by a novel, biologically informed polygenetic score based on the serotonin transporter solute carrier family C6, member 4 (SLC6A4) gene expression. Development and psychopathology 2017 Dec 29 (5): 1601-1617. Silveira Patrícia P, Pokhvisneva Irina, Parent Carine, Cai Shirong, Rema Anu Sathyan Sathyapalan, Broekman Birit F P, Rifkin-Graboi Anne, Pluess Michael, O'Donnell Kieran J, Meaney Michael |
Alzheimer Disease and Selected Risk Factors Disrupt a Co-regulation of Monoamine Oxidase-A/B in the Hippocampus, but Not in the Cortex. Frontiers in neuroscience 2018 12 419. Quartey Maa O, Nyarko Jennifer N K, Pennington Paul R, Heistad Ryan M, Klassen Paula C, Baker Glen B, Mousseau Darrell |
Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 2020 8 13 (5): 396-405. Helms Adam S, Thompson Andrea D, Glazier Amelia A, Hafeez Neha, Kabani Samat, Rodriguez Juliani, Yob Jaime M, Woolcock Helen, Mazzarotto Francesco, Lakdawala Neal K, Wittekind Samuel G, Pereira Alexandre C, Jacoby Daniel L, Colan Steven D, Ashley Euan A, Saberi Sara, Ware James S, Ingles Jodie, Semsarian Christopher, Michels Michelle, Olivotto Iacopo, Ho Carolyn Y, Day Sharlene |
Cocaine-Induced Sensitization is Linked to Distal Chromosome 6 Region in Congenic Mouse Model. Drug and alcohol dependence 2020 8 215 108185. Vadasz Csaba, Gyetvai Beatrix |
Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Jul . Squitieri Ferdinando, Mazza Tommaso, Maffi Sabrina, De Luca Alessandro, AlSalmi Qasem, AlHarasi Salma, Collins Jennifer A, Kay Chris, Baine-Savanhu Fiona, Landwhermeyer Bernard G, Sabatini Umberto, Hayden Michael |
Hb Athens-Georgia (beta 40(C6) Arg?>?Lys, HBB:c.122G?>?A) with a single ?-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scandinavian journal of clinical and laboratory investigation 2020 Dec 1-7. Panyasai Sitthichai, Kunyanone Naowarat, Satthakarn Sura |
Determination of genetic effects and functional SNPs of bovine HTR1B gene on milk fatty acid traits. BMC genomics 2021 7 22 (1): 575. Cao Mingyue, Shi Lijun, Peng Peng, Han Bo, Liu Lin, Lv Xiaoqing, Ma Zhu, Zhang Shengli, Sun Dongxi |
Identification of a novel mutation in the C6 gene of a Han Chinese C6SD child with meningococcal disease. Experimental and therapeutic medicine 2021 4 21 (5): 510. Zhang Ai-Qian, Liu Yu-Xing, Jin Jie-Yuan, Wang Chen-Yu, Fan Liang-Liang, Xu Da-B |
The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease. The Turkish journal of pediatrics 2021 63 (1): 118-125. Balamtekin Necati, Baysoy Gökhan, Tan Ça?man, K?z?lkan Nuray Uslu, Demir Hülya, Salt?k-Temizel ?nci Nur, Özen Hasan, Yüce Aysel, Tezcan ?lhan, Gürakan Fig |
Moyamoya Disease Associated with a Deficiency of Complement Component 6. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2022 Jun 31 (8): 106601. Kato Masaru, Kudo Yuki, Hatase Masanao, Tsuchida Naohisa, Takeyama Shuhei, Sugiyama Taku, Fujimura Miki, Yabe Ichiro, Tsujimoto Hiroshi, Fukumori Yasuo, Inoue Norimitsu, Atsumi Tatsu |
Tacrolimus dose adjustment is not necessary in dose to dose conversion from a twice daily to a prolonged release once daily dose form. Scientific reports 2022 6 12 (1): 10051. Tiankanon Kanitha, Kerr Stephen J, Thongthip Siriwan, Udomkarnjananun Suwasin, Sodsai Pimpayao, Vorasittha Athaya, Panumatrassamee Kamol, Takkavatakarn Kullaya, Tungsanga Kriang, Eiam-Ong Somchai, Praditpornsilpa Kearkiat, Avihingsanon Yingyos, Townamchai Natavu |
Identification of a Five-Gene Panel to Assess Prognosis for Gastric Cancer. BioMed research international 2022 2022 5593619. Li Shuxin, Mao Qianqian, Zhang Zixuan, Wang Yuqi, Chen Duoxuan, Chen Zhenwen, Lu Jian |
Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation. Frontiers in immunology 2023 9 14 1249958. Lilli Leimi, Jessica R Koski, Outi Kilpivaara, Kim Vettenranta, A Inkeri Lokki, Seppo Me |
Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers. Journal of cardiovascular translational research 2023 6 . Mark Jansen, A F Schmidt, J J M Jans, I Christiaans, S N van der Crabben, Y M Hoedemaekers, D Dooijes, J D H Jongbloed, L G Boven, R H Lekanne Deprez, A A M Wilde, J van der Velden, R A de Boer, J P van Tintelen, F W Asselbergs, A F Ba |
Whole exome sequencing reveal 83 novel Mendelian disorders carrier P/LP variants in Chinese adult patients. Journal of human genetics 2023 6 . Li Zhang, Li Yu, Xianhong Shu, Jing Ding, Jingmin Zhou, Chunjiu Zhong, Baishen Pan, Wei Guo, Chunyan Zhang, Beili Wa |
Molecular Typing of Mastadenoviruses in Simultaneously Collected Nasopharyngeal Swabs and Stool Samples from Children Hospitalized for Acute Bronchiolitis, Acute Gastroenteritis, and Febrile Seizures. Microorganisms 2023 3 11 (3): . Biškup Urška Glinšek, Steyer Andrej, Lusa Lara, Strle Franc, Pokorn Marko, Mrvi? Tatjana, Grosek Štefan, Petrovec Miroslav, Jevšnik Virant Moni |
Impact of genetic polymorphisms on tacrolimus trough blood concentration in Chinese liver transplant recipients. Pharmacogenomics 2023 3 24 (4): 207-217. Maseko Nicola, Yang Siyao, Li Chengcheng, Zhang Siqi, Wang Ruiying, Zhang Yawen, Li Chuanjiang, Zhang Chuanjie, Li Lia |
A Systematic Pan-Cancer Analysis of MEIS1 in Human Tumors as Prognostic Biomarker and Immunotherapy Target. Journal of clinical medicine 2023 2 12 (4): . Li Han, Tang Ying, Hua Lichun, Wang Zemin, Du Guoping, Wang Shuai, Lu Shifeng, Li W |
Metabolic heterogeneity in early-stage lung adenocarcinoma revealed by RNA-seq and scRNA-seq. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 1 . Zhang Yang, Shi Jiang, Luo Junfang, Liu Cong, Zhu Li |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: