Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 174 Records) |
| Query Trace: Gene therapy[original query] |
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| PD-L1 is prognostic and a negative predictor of response to immunotherapy in gastric cancer. Molecular therapy : the journal of the American Society of Gene Therapy 2021 9 30 (2): 621-631. Li Qing, Zhou Zhi-Wei, Lu Jia, Luo Hao, Wang Shu-Nan, Peng Yu, Deng Meng-Sheng, Song Guan-Bin, Wang Jian-Min, Wei Xi, Wang Dong, Westover Kenneth D, Xu Cheng-Xio |
| The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study. Human genetics 2021 8 141 (3-4): 853-863. Thorpe Ryan K, Azaiez Hela, Wu Peina, Wang Qiuju, Xu Lei, Dai Pu, Yang Tao, Schaefer G Bradley, Peters B Robert, Chan Kenny H, Schatz Krista S, Bodurtha Joann, Robin Nathaniel H, Hirsch Yoel, Rahbeeni Zuhair Abdalla, Yuan Huijun, Smith Richard J |
| Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population. Orphanet journal of rare diseases 2021 5 16 (1): 174. Gao Feng-Juan, Wang Dan-Dan, Li Jian-Kang, Hu Fang-Yuan, Xu Ping, Chen Fang, Qi Yu-He, Liu Wei, Li Wei, Zhang Sheng-Hai, Chang Qing, Xu Ge-Zhi, Wu Ji-Ho |
| The Relationship of Leptin (+19) AG, Leptin (2548) GA, and Leptin Receptor Gln223Arg Gene Polymorphisms with Obesity and Metabolic Syndrome in Obese Children and Adolescents. Pediatric gastroenterology, hepatology & nutrition 2021 5 24 (3): 306-315. Bilge Serap, Y?lmaz Resul, Karaslan Erhan, Özer Samet, Ate? Ömer, Ensari Emel, Demir Osm |
| Analysis of Adenoviral p53 Gene Therapy Clinical Trials in Recurrent Head and Neck Squamous Cell Carcinoma. Frontiers in oncology 2021 5 11 645745. Sobol Robert E, Menander Kerstin B, Chada Sunil, Wiederhold Dora, Sellman Beatha, Talbott Max, Nemunaitis John |
| Risk Assessment Using the Association Between Renin-Angiotensin Genes Polymorphisms and Coronary Artery Disease. Cureus 2021 4 13 (3): e14083. Riad Mohamed, Adhikari Prakash, Bhattarai Sanket, Gupta Ashish, Ali Eiman, Ali Moeez, Mostafa Jihan |
| The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascade. Human molecular genetics 2021 3 30 (13): 1188-1199. McMahon O, Hallam T M, Patel S, Harris C L, Menny A, Zelek W M, Widjajahakim R, Java A, Cox T E, Tzoumas N, Steel D H W, Shuttleworth V G, Smith-Jackson K, Brocklebank V, Griffiths H, Cree A J, Atkinson J P, Lotery A J, Bubeck D, Morgan B P, Marchbank K J, Seddon J M, Kavanagh |
| Susceptibility to ischaemic heart disease: Focusing on genetic variants for ATP-sensitive potassium channel beyond traditional risk factors. European journal of preventive cardiology 2021 2 . Severino Paolo, D'Amato Andrea, Netti Lucrezia, Pucci Mariateresa, Mariani Marco V, Cimino Sara, Birtolo Lucia I, Infusino Fabio, De Orchi Paolo, Palmirotta Raffaele, Lovero Domenica, Silvestris Franco, Caputo Viviana, Pizzuti Antonio, Miraldi Fabio, Maestrini Viviana, Mancone Massimo, Fedele Frances |
| MicroRNAs in ?-thalassemia. The American journal of the medical sciences 2021 2 362 (1): 5-12. Wang Fangfang, Ling Ling, Yu Duon |
| Genetic Polymorphism of Drug Metabolic Gene CYPs, VKORC1, NAT2, DPYD and CHST3 of Five Ethnic Minorities in Heilongjiang Province, Northeast China. Pharmacogenomics and personalized medicine 2021 12 14 1537-1547. Zhang Tingting, Li Qiuyan, Dong Bonan, Liang Xiao, Jia Mansha, Bai Jing, Yu Jingcui, Fu Songb |
| Impact of FLT3 internal tandem duplication and NPM1 mutations in acute myeloid leukemia treated with allogeneic hematopoietic cell transplantation. Cytotherapy 2021 Dec . Khanolkar Rutvij A, Faridi Rehan M, Kinzel Megan, Jamani Kareem, Savoie Mary L, Shafey Mona, Khan Faisal M, Storek J |
| A Clinical Prediction Model to Determine Probability of Response to Certolizumab Pegol for Crohn's Disease. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy 2021 12 36 (1): 85-93. Lefevre Pavine L C, Dulai Parambir S, Wang Zhongya, Guizzetti Leonardo, Feagan Brian G, Pop Anca, Yassine Mohamed, Shackelton Lisa M, Jairath Vipul, Sandborn William J, Vande Casteele Nie |
| Network based analysis identifies TP53m-BRCA1/2wt-homologous recombination proficient (HRP) population with enhanced susceptibility to Vigil immunotherapy. Cancer gene therapy 2021 11 29 (7): 993-1000. Sliheet Elyssa, Robinson Molly, Morand Susan, Choucair Khalil, Willoughby David, Stanbery Laura, Aaron Phylicia, Bognar Ernest, Nemunaitis Jo |
| Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population. Frontiers in genetics 2021 10 12 741355. Ji Zhiyong, Yao Chencheng, Yang Chao, Huang Chuan, Zhao Liangyu, Han Xia, Zhu Zijue, Zhi Erlei, Liu Nachuan, Zhou Zhi, Li Zhe |
| The cross-talk of cancer-associated fibroblasts assist in prognosis and immunotherapy in patients with breast carcinoma. Cancer gene therapy 2022 Aug . Gu Xuyu, Zheng Shiya, Zhang Haifeng, Sun Xiaotong, Zhou Q |
| Evaluation of clonal hematopoiesis in pediatric ADA-SCID gene therapy participants. Blood advances 2022 8 6 (21): 5732-5736. White Shanna L, Lee Thomas D, Toy Traci, Carroll Judith E, Polsky Lilian, Campo Fernandez Beatriz, Davila Alejandra, Kohn Donald B, Chang Vivian |
| The Clinically Actionable Molecular Profile of Early versus Late-Stage Non-Small Cell Lung Cancer, an Individual Age and Sex Propensity-Matched Pair Analysis. Current oncology (Toronto, Ont.) 2022 4 29 (4): 2630-2643. McGuire Anna L, McConechy Melissa K, Melosky Barb L, English John C, Choi James J, Peng Defen, Yee John, Furman Benjamin L S, Aguirre Hernandez Rosalia, Feijao Pedro, Mulder David, Hughesman Curtis, Yip Steph |
| Congenital Stationary Night Blindness: Clinical and Genetic Features. International journal of molecular sciences 2022 12 23 (23): . Kim Angela H, Liu Pei-Kang, Chang Yin-Hsi, Kang Eugene Yu-Chuan, Wang Hung-Hsuan, Chen Nelson, Tseng Yun-Ju, Seo Go Hun, Lee Hane, Liu Laura, Chao An-Ning, Chen Kuan-Jen, Hwang Yih-Shiou, Wu Wei-Chi, Lai Chi-Chun, Tsang Stephen H, Hsiao Meng-Chang, Wang Nan-K |
| Randomized trial of bilateral gene therapy injection for m.11778G?>?A MT-ND4 Leber optic neuropathy. Brain : a journal of neurology 2022 11 . Newman Nancy J, Yu-Wai-Man Patrick, Subramanian Prem S, Moster Mark L, Wang An-Guor, Donahue Sean P, Leroy Bart P, Carelli Valerio, Biousse Valerie, Vignal-Clermont Catherine, Sergott Robert C, Sadun Alfredo A, Fernández Gema Rebolleda, Chwalisz Bart K, Banik Rudrani, Bazin Fabienne, Roux Michel, Cox Eric D, Taiel Magali, Sahel José-Alain, |
| Molecular background of Leber congenital amaurosis in a Polish cohort of patients-novel variants discovered by NGS. Journal of applied genetics 2022 11 64 (1): 89-104. Skorczyk-Werner Anna, Sowi?ska-Seidler Anna, Wawrocka Anna, Walczak-Sztulpa Joanna, Krawczy?ski Maciej Robe |
| Carrier frequency and incidence estimation of RPE65-associated inherited retinal diseases in East Asian population by population database-based analysis. Orphanet journal of rare diseases 2022 11 17 (1): 409. Cho Eun Hye, Park Jong Eun, Lee Taeheon, Ha Kyeongsu, Ki Chang-Se |
| Retinitis Punctata Albescens and RLBP1-Allied Phenotypes: Phenotype-Genotype Correlation and Natural History in the Aim of Gene Therapy. Ophthalmology science 2022 10 1 (3): 100052. Bocquet Béatrice, El Alami Trebki Hicham, Roux Anne Françoise, Labesse Gilles, Brabet Philippe, Arndt Carl, Zanlonghi Xavier, Defoort-Dhellemmes Sabine, Hamroun Dalil, Boulicot-Séguin Céline, Lequeux Léopoldine, Picot Marie Christine, Huguet Hélèna, Audo Isabelle, Dhaenens Claire Marie, Kalatzis Vasiliki, Meunier Isabel |
| Influence of Haptoglobin Polymorphism on Stroke in Sickle Cell Disease Patients. Genes 2022 1 13 (1): . Edwards Olivia, Burris Alicia, Lua Josh, Wilkie Diana J, Ezenwa Miriam O, Doré Sylva |
| Somatic copy number alteration predicts clinical benefit of lung adenocarcinoma patients treated with cytokine-induced killer plus chemotherapy. Cancer gene therapy 2022 1 29 (8-9): 1153-1159. Kou Fan, Wu Lei, Zhu Ye, Li Baihui, Huang Ziqi, Ren Xiubao, Yang Li |
| Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 2023 4 14 (4): . Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berg |
| Cost-effective genotyping for classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) in resource-poor settings: multiplex ligation probe amplification (MLPA) with/without sequential next-generation sequencing (NGS). Hormones (Athens, Greece) 2023 3 . Monteiro Ana, Pavithran Praveen V, Puthukulangara Manuprasad, Bhavani Nisha, Nampoothiri Sheela, Yesodharan Dhanya, Kumaran Resh |
| Benefits of plerixafor for mobilization of peripheral blood stem cells prior to autologous transplantation: a dual-center retrospective cohort study. Cytotherapy 2023 3 . Nakamura Naokazu, Jo Tomoyasu, Arai Yasuyuki, Matsumoto Mayumi, Sakai Tomomi, Tsunemine Hiroko, Takaori-Kondo Akifumi, Arima Nobuyos |
| Next-generation sequencing approach to molecular diagnosis of Iranian patients with Duchenne/Becker muscular dystrophy: Several novel variants identified. eNeurologicalSci 2023 2 30 100446. Bakhshandeh MohammadKazem, Behroozi Sami |
| Whole Exome Sequencing Identified Two Single Nucleotide Polymorphisms of Human Leukocyte Antigen-DRB5 in Familial Sarcoidosis in China. Current gene therapy 2023 1 . Zhang Qian, Xu Zuojun, Huang Hui, Zhang Meij |
| Interaction of environmental factors with the polygenic risk scores of thinness-related genes in preventing obesity risk in middle-aged adults: The KoGES. Journal of human nutrition and dietetics : the official journal of the British Dietetic Association 2023 1 . Zhou Jun-Yu, Liu Meiling, Park Sunm |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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