Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: NRP1[original query] |
---|
The altered expression of syndecan 4 in the uninvolved skin of venous leg ulcer patients may predispose to venous leg ulcer. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 0 16 (4): 495-502. Nagy Nikoletta, Németh István Balázs, Szabad Gábor, Szolnoky Gyõzõ, Belsõ Nóra, Bata-Csörgõ Zsuzsanna, Dobozy Attila, Kemény Lajos, Széll Már |
Cetuximab as second-line therapy in patients with metastatic esophageal adenocarcinoma: a phase II Southwest Oncology Group Study (S0415). Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2010 Sep 5 (9): 1472-6. Gold Philip J, Goldman Bryan, Iqbal Syma, Leichman Lawrence P, Zhang Wu, Lenz Heinz-Josef, Blanke Charles |
Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head. Experimental & molecular medicine 2010 May 42 (5): 376-85. Hong Jung Min, Kim Tae Ho, Kim Hyun Ju, Park Eui Kyun, Yang Eun Kyoung, Kim Shin Yo |
Molecular predictors of combination targeted therapies (cetuximab, bevacizumab) in irinotecan-refractory colorectal cancer (BOND-2 study). Anticancer research 2010 Oct 30 (10): 4209-17. Zhang Wu, Azuma Mizutomo, Lurje Georg, Gordon Michael A, Yang Dongyun, Pohl Alexandra, Ning Yan, Bohanes Pierre, Gerger Armin, Winder Thomas, Hollywood Ellen, Danenberg Kathleen D, Saltz Leonard, Lenz Heinz-Jos |
Genetic association of the neuropilin-1 gene with type 1 diabetes in children: Neuropilin-1 expression in pancreatic islets. Diabetes research and clinical practice 2010 Jan . Hasan Noaman M, Kendrick Mindy A, Druckenbrod Noah R, Huelsmeyer Michael K, Warner Thomas F, MacDonald Michael |
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies. Congenital heart disease 0 6 (6): 592-602. Goldmuntz Elizabeth, Paluru Prasuna, Glessner Joseph, Hakonarson Hakon, Biegel Jaclyn A, White Peter S, Gai Xiaowu, Shaikh Tamim |
Vascular endothelial growth factor pathway polymorphisms as prognostic and pharmacogenetic factors in cancer: a systematic review and meta-analysis. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Sep 18 (17): 4526-37. Eng Lawson, Azad Abul Kalam, Habbous Steven, Pang Vincent, Xu Wei, Maitland-van der Zee Anke H, Savas Sevtap, Mackay Helen J, Amir Eitan, Liu Geoffr |
Genetic variants at 10p11 confer risk of Tetralogy of Fallot in Chinese of Nanjing. PloS one 2014 9 (3): e89636. Xu Jing, Lin Yuan, Si Linjie, Jin Guangfu, Dai Juncheng, Wang Cheng, Chen Jiaping, Da Min, Hu Yuanli, Yi Chenlong, Hu Zhibin, Shen Hongbing, Mo Xuming, Chen Yijiang, Wang Xiaow |
A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations. Genetic epidemiology 2014 Dec 38 (8): 661-70. Evangelou Marina, Smyth Deborah J, Fortune Mary D, Burren Oliver S, Walker Neil M, Guo Hui, Onengut-Gumuscu Suna, Chen Wei-Min, Concannon Patrick, Rich Stephen S, Todd John A, Wallace Chr |
Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 691-704. Smith Taylor F, Anastopoulos Arthur D, Garrett Melanie E, Arias-Vasquez Alejandro, Franke Barbara, Oades Robert D, Sonuga-Barke Edmund, Asherson Philip, Gill Michael, Buitelaar Jan K, Sergeant Joseph A, Kollins Scott H, Faraone Stephen V, Ashley-Koch Allison, |
Neuronal cell adhesion genes and antidepressant response in three independent samples. The pharmacogenomics journal 2015 Apr . Fabbri C, Crisafulli C, Gurwitz D, Stingl J, Calati R, Albani D, Forloni G, Calabrò M, Martines R, Kasper S, Zohar J, Juven-Wetzler A, Souery D, Montgomery S, Mendlewicz J, Girolamo G D, Serretti |
A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degeneration. Pharmacogenetics and genomics 2015 Sep . Lorés-Motta Laura, van Asten Freekje, Muether Philipp S, Smailhodzic Dzenita, Groenewoud Joannes M, Omar Amer, Chen John, Koenekoop Robert K, Fauser Sascha, Hoyng Carel B, den Hollander Anneke I, de Jong Eiko |
HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes. PloS one 2017 11 12 (11): e0188402. Parkkola Anna, Laine Antti-Pekka, Karhunen Markku, Härkönen Taina, Ryhänen Samppa J, Ilonen Jorma, Knip Mikael, |
The NRP1 migraine risk variant shows evidence of association with menstrual migraine. The journal of headache and pain 2018 Apr 19 (1): 31. Pollock Charmaine E, Sutherland Heidi G, Maher Bridget H, Lea Rodney A, Haupt Larisa M, Frith Alison, Anne MacGregor E, Griffiths Lyn |
Genotyping and mRNA profiling reveal actionable molecular targets in biliary tract cancers. American journal of cancer research 2018 2 8 (1): 2-15. Papadopoulou Kyriaki, Murray Samuel, Manousou Kyriaki, Tikas Ioannis, Dervenis Christos, Sgouros Joseph, Rontogianni Dimitra, Lakis Sotirios, Bobos Mattheos, Poulios Christos, Pervana Stavroula, Lazaridis Georgios, Fountzilas George, Kotoula Vassili |
Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population. Gene 2018 Feb . Fan Sai-Hou, Shen Zhen-Ya, Xiao Yi-M |
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical genetics 2019 Feb 95 (2): 320-324. Kotan Leman D, Isik Emregul, Turan Ihsan, Mengen Eda, Akkus Gamze, Tastan Mehmet, Gurbuz Fatih, Yuksel Bilgin, Topaloglu A Kem |
APOE ?4-specific associations of VEGF gene family expression with cognitive aging and Alzheimer's disease. Neurobiology of aging 2019 12 87 18-25. Moore Annah M, Mahoney Emily, Dumitrescu Logan, De Jager Philip L, Koran Mary Ellen I, Petyuk Vladislav A, Robinson Renã As, Ruderfer Douglas M, Cox Nancy J, Schneider Julie A, Bennett David A, Jefferson Angela L, Hohman Timothy |
Identification of novel loci influencing refractive error in East Asian populations using an extreme phenotype design. Journal of genetics and genomics = Yi chuan xue bao 2021 Sep . Han Xiaotong, Liu Tianzi, Ding Xiaohu, Liu Jialin, Lin Xingyan, Wang Decai, Riaz Moeen, Baird Paul N, Xie Zhi, Cheng Yuan, Li Yi, Mori Yuki, Miyake Masahiro, Li Hengtong, Cheng Ching-Yu, Zeng Changqing, Ohno-Matsui Kyoko, Zhou Xiangtian, Liu Fan, He Minggua |
Age- and airway disease related gene expression patterns of key SARS-CoV-2 entry factors in human nasal epithelia. Virology 2021 6 561 65-68. Plaas Mihkel, Seppa Kadri, Gaur Nayana, Kasenõmm Priit, Plaas Mar |
Pancancer Analysis of Neurovascular-Related NRP Family Genes as Potential Prognostic Biomarkers of Bladder Urothelial Carcinoma. BioMed research international 2021 5 2021 5546612. Deng Chao, Guo Hang, Yan Dongliang, Liang Tao, Ye Xuxiao, Li Zuow |
Genetics of PlGF plasma levels highlights a role of its receptors and supports the link between angiogenesis and immunity.
Scientific reports 2021 8 11 (1): 16821. Ruggiero Daniela, Nutile Teresa, Nappo Stefania, Tirozzi Alfonsina, Bellenguez Celine, Leutenegger Anne-Louise, Ciullo Mari |
Hypoxia Confers Tumor with a Higher Immune Infiltration but Lower Mutation Burden in Gastrointestinal Cancer. Journal of oncology 2022 9 2022 4965167. Hu Junjie, Hu Wangxiong, Yang Yanm |
Non-HLA Gene Polymorphisms in the Pathogenesis of Type 1 Diabetes: Phase and Endotype Specific Effects. Frontiers in immunology 2022 13 909020. Laine Antti-Pekka, Valta Milla, Toppari Jorma, Knip Mikael, Veijola Riitta, Ilonen Jorma, Lempainen Johan |
A Novel Intron-Encoded Neuropilin-1 Isoform in Pancreatic Islets Associated With Very Young Age of Onset of Type 1 Diabetes. Diabetes 2022 6 71 (9): 2058-2063. MacDonald Michael J, Ansari Israr-Ul H, Riedemann Amy S, Stoker Scott W, Eickhoff Jens C, Chlebeck Peter J, Fernandez Luis A, Longacre Melissa |
Construction of ovarian metastasis-related immune signature predicting prognosis of gastric cancer patients. Cancer medicine 2022 May . Gao Jianpeng, Huo Shiying, Zhang Yu, Zhao Zhenxiong, Pan Hongda, Liu Xiaow |
Attenuation of SARS-CoV-2 infection by losartan in human kidney organoids. iScience 2022 2 25 (2): 103818. Rahmani Waleed, Chung Hyunjae, Sinha Sarthak, Bui-Marinos Maxwell P, Arora Rohit, Jaffer Arzina, Corcoran Jennifer A, Biernaskie Jeff, Chun Just |
Association between SEMA3A signaling pathway genes and BMD/OP risk: An epidemiological and experimental study. Frontiers in endocrinology 2022 11 13 1014431. Zhou Hao-Long, Wei Mu-Hong, Di Dong-Sheng, Zhang Ru-Yi, Zhang Jian-Li, Yuan Ting-Ting, Liu Qian, Zhou Ting-Ting, Huang Qin, Wang |
Immune inactivation by neuropilin-1 predicts clinical outcome and therapeutic benefit in muscle-invasive bladder cancer. Cancer immunology, immunotherapy : CII 2022 1 71 (9): 2117-2126. Yu Yanze, Zeng Han, Jin Kaifeng, You Runze, Liu Zhaopei, Zhang Hongyi, Liu Chunnan, Su Xiaohe, Yan Sen, Chang Yuan, Liu Li, Xu Le, Xu Jiejie, Zhu Yu, Wang Zew |
Polymorphisms within the SARS-CoV-2 Human Receptor Genes Associate with Variable Disease Outcomes across Ethnicities. Genes 2023 9 14 (9): . Theolan Adimulam, Thilona Arumugam, Anushka Naidoo, Kogieleum Naidoo, Veron Ramsur |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: