Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 50 Records) |
Query Trace: RAC1[original query] |
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Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability. Nature neuroscience 2016 Aug . Lelieveld Stefan H, Reijnders Margot R F, Pfundt Rolph, Yntema Helger G, Kamsteeg Erik-Jan, de Vries Petra, de Vries Bert B A, Willemsen Marjolein H, Kleefstra Tjitske, Löhner Katharina, Vreeburg Maaike, Stevens Servi J C, van der Burgt Ineke, Bongers Ernie M H F, Stegmann Alexander P A, Rump Patrick, Rinne Tuula, Nelen Marcel R, Veltman Joris A, Vissers Lisenka E L M, Brunner Han G, Gilissen Christi |
Rho GTPases: RAC1 polymorphisms affected platinum-based chemotherapy toxicity in lung cancer patients. Cancer chemotherapy and pharmacology 2016 Aug 78 (2): 249-58. Zou Ting, Yin Jiye, Zheng Wei, Xiao Ling, Tan Liming, Chen Juan, Wang Ying, Li Xiangping, Qian Chenyue, Cui Jiajia, Zhang Wei, Zhou Honghao, Liu Zhaoqi |
Identification and association of RAC1 gene polymorphisms with mRNA and protein expression levels of Rac1 in solid organ (kidney, liver, heart) transplant recipients. Molecular medicine reports 2016 Jun . Zhou Jiali, Liu Yani, Luo Xiaomei, Shen Rufei, Yang Chunxiao, Yang Tingyu, Shi Shaoj |
A mutation in Nischarin causes otitis media via LIMK1 and NF-?B pathways. PLoS genetics 2017 Aug 13 (8): e1006969. Crompton Michael, Purnell Tom, Tyrer Hayley E, Parker Andrew, Ball Greg, Hardisty-Hughes Rachel E, Gale Richard, Williams Debbie, Dean Charlotte H, Simon Michelle M, Mallon Ann-Marie, Wells Sara, Bhutta Mahmood F, Burton Martin J, Tateossian Hilda, Brown Steve D |
Urine cadmium levels and albuminuria in a general population from Spain: A gene-environment interaction analysis. Environment international 2017 May 106 27-36. Grau-Perez Maria, Pichler Gernot, Galan-Chilet Inma, Briongos-Figuero Laisa S, Rentero-Garrido Pilar, Lopez-Izquierdo Raul, Navas-Acien Ana, Weaver Virginia, García-Barrera Tamara, Gomez-Ariza Jose L, Martín-Escudero Juan C, Chaves F Javier, Redon Josep, Tellez-Plaza Mar |
Association analysis of RAC1 single nucleotide polymorphisms with ulcerative colitis. Clinics and research in hepatology and gastroenterology 2017 Apr . Taher Mohammad, Ebrahimi Daryani Nasser, Hedayat Mona, Eslamian Mohammad, Farhadi Elham, Mahmoudi Mahdi, Shirzad Samira, Nouri Taromlou Mohammd Kazem, Chaharmahali Meghedi, Nicknam Mohammad Hossein, Bashashati Mohammad, Rezaei Ni |
Associations Between Genetic Variants of NADPH Oxidase-Related Genes and Blood Pressure Responses to Dietary Sodium Intervention: The GenSalt Study. American journal of hypertension 2017 Feb . Han Xikun, Hu Zunsong, Chen Jing, Huang Jianfeng, Huang Chen, Liu Fangchao, Gu Charles, Yang Xueli, Hixson James E, Lu Xiangfeng, Wang Laiyuan, Liu De-Pei, He Jiang, Chen Shufeng, Gu Dongfe |
Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function. Human molecular genetics 2017 10 26 (20): 4011-4027. Lee Mei-Chin, Shei William, Chan Anita S, Chua Boon-Tin, Goh Shuang-Ru, Chong Yaan-Fun, Hilmy Maryam H, Nongpiur Monisha E, Baskaran Mani, Khor Chiea-Chuen, Aung Tin, Hunziker Walter, Vithana Eranga |
Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease. Gastroenterology 2018 2 154 (8): 2097-2110. Denson Lee A, Jurickova Ingrid, Karns Rebekah, Shaw Kelly A, Cutler David J, Okou David T, Dodd Anne, Quinn Kathryn, Mondal Kajari, Aronow Bruce J, Haberman Yael, Linn Aaron, Price Adam, Bezold Ramona, Lake Kathleen, Jackson Kimberly, Walters Thomas D, Griffiths Anne, Baldassano Robert N, Noe Joshua D, Hyams Jeffrey S, Crandall Wallace V, Kirschner Barbara S, Heyman Melvin B, Snapper Scott, Guthery Stephen L, Dubinsky Marla C, Leleiko Neal S, Otley Anthony R, Xavier Ramnik J, Stevens Christine, Daly Mark J, Zwick Michael E, Kugathasan Sub |
A Case-Control Study of the Genetic Variability in Reactive Oxygen Species-Metabolizing Enzymes in Melanoma Risk. International journal of molecular sciences 2018 Jan 19 (1): . Yuan Tze-An, Yourk Vandy, Farhat Ali, Ziogas Argyrios, Meyskens Frank L, Anton-Culver Hoda, Liu-Smith Fe |
The Prognostic Significance of Low-Frequency Somatic Mutations in Metastatic Cutaneous Melanoma. Frontiers in oncology 2019 1 8 584. Zhao Xiaobei, Little Paul, Hoyle Alan P, Pegna Guillaume J, Hayward Michele C, Ivanova Anastasia, Parker Joel S, Marron David L, Soloway Matthew G, Jo Heejoon, Salazar Ashley H, Papakonstantinou Michael P, Bouchard Deeanna M, Jefferys Stuart R, Hoadley Katherine A, Ollila David W, Frank Jill S, Thomas Nancy E, Googe Paul B, Ezzell Ashley J, Collichio Frances A, Lee Carrie B, Earp H Shelton, Sharpless Norman E, Hugo Willy, Wilmott James S, Quek Camelia, Waddell Nicola, Johansson Peter A, Thompson John F, Hayward Nicholas K, Mann Graham J, Lo Roger S, Johnson Douglas B, Scolyer Richard A, Hayes D Neil, Moschos Stergios |
A noncanonical role for the engulfment gene ELMO1 in neutrophils that promotes inflammatory arthritis. Nature immunology 2019 1 20 (2): 141-151. Arandjelovic Sanja, Perry Justin S A, Lucas Christopher D, Penberthy Kristen K, Kim Tae-Hyoun, Zhou Ming, Rosen Dorian A, Chuang Tzu-Ying, Bettina Alexandra M, Shankman Laura S, Cohen Amanda H, Gaultier Alban, Conrads Thomas P, Kim Minsoo, Elliott Michael R, Ravichandran Kodi |
Bioinformatic analysis of the potential molecular mechanism of PAK7 expression in glioblastoma. Molecular medicine reports 2020 7 22 (2): 1362-1372. Wang Xuefeng, Liu Shuang, Shao Zhengkai, Zhang Pengh |
RAS/MAPK Pathway Driver Alterations Are Significantly Associated With Oncogenic KIT Mutations in Germ-cell Tumors. Urology 2020 7 144 111-116. Mata Douglas A, Yang Soo-Ryum, Ferguson Donna C, Liu Ying, Sharma Rohit, Benhamida Jamal K, Al-Ahmadie Hikmat A, Chakravarty Debyani, Solit David B, Tickoo Satish K, Gupta Sounak, Arcila Maria E, Ladanyi Marc, Feldman Darren R, Reuter Victor E, Vanderbilt Chad |
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay. Annals of clinical and translational neurology 2020 5 7 (6): 956-964. Asiri Abdulaziz, Aloyouni Essra, Umair Muhammad, Alyafee Yusra, Al Tuwaijri Abeer, Alhamoudi Kheloud M, Almuzzaini Bader, Al Baz Abeer, Alwadaani Deemah, Nashabat Marwan, Alfadhel Maj |
Genetic Profiling of Advanced Melanoma: Candidate Mutations for Predicting Sensitivity and Resistance to Targeted Therapy. Targeted oncology 2020 1 15 (1): 101-113. Olbryt Magdalena, Pig?owski Wojciech, Rajczykowski Marcin, Pfeifer Aleksandra, Student Sebastian, Fiszer-Kierzkowska An |
Retinopathy in a Diet-Induced Type 2 Diabetic Rat Model and Role of Epigenetic Modifications. Diabetes 2020 Jan . Kowluru Renu |
Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.
Nature metabolism 2021 02 3 (2): 228-243. Huang Lam O, Rauch Alexander, Mazzaferro Eugenia, Preuss Michael, Carobbio Stefania, Bayrak Cigdem S, Chami Nathalie, Wang Zhe, Schick Ursula M, Yang Nancy, Itan Yuval, Vidal-Puig Antonio, den Hoed Marcel, Mandrup Susanne, Kilpeläinen Tuomas O, Loos Ruth J |
Somatic Mutational Profile of High-Grade Serous Ovarian Carcinoma and Triple-Negative Breast Carcinoma in Young and Elderly Patients: Similarities and Divergences. Cells 2021 12 10 (12): . Serio Pedro Adolpho de Menezes Pacheco, de Lima Pereira Gláucia Fernanda, Katayama Maria Lucia Hirata, Roela Rosimeire Aparecida, Maistro Simone, Folgueira Maria Aparecida Azevedo Koi |
Estrogen receptor alpha and NFATc1 bind to a bone mineral density-associated SNP to repress WNT5B in osteoblasts. American journal of human genetics 2021 12 109 (1): 97-115. Suthon Sarocha, Lin Jianjian, Perkins Rachel S, Crockarell John R, Miranda-Carboni Gustavo A, Krum Susan |
Mutational Characterization of Cutaneous Melanoma Supports Divergent Pathways Model for Melanoma Development. Cancers 2021 10 13 (20): . Millán-Esteban David, Peña-Chilet María, García-Casado Zaida, Manrique-Silva Esperanza, Requena Celia, Bañuls José, López-Guerrero Jose Antonio, Rodríguez-Hernández Aranzazu, Traves Víctor, Dopazo Joaquín, Virós Amaya, Kumar Rajiv, Nagore Eduar |
Protein Network Analysis of Whole Exome Sequencing of Severe Preeclampsia. Frontiers in genetics 2022 6 12 765985. Schuster Jessica, Tollefson George A, Zarate Valeria, Agudelo Anthony, Stabila Joan, Ragavendran Ashok, Padbury James, Uzun Alp |
Mutational pattern of PIK3CA exon 20 in circulating DNA in breast cancer. Saudi journal of biological sciences 2022 5 29 (4): 2828-2835. Ibrahim Iman Hassan, Abd El-Aziz Heba Gamal, Amer Noha Nagah Labib, Abd El-Sameea Hesham Sam |
Association between RAC1 gene variation, redox homeostasis and type 2 diabetes mellitus. European journal of clinical investigation 2022 4 52 (8): e13792. Azarova Iuliia, Klyosova Elena, Polonikov Alex |
Genomic characterisation of de novo EGFR copy number gain and its impact on the efficacy of first-line EGFR-tyrosine kinase inhibitors for EGFR mutated non-small cell lung cancer. European journal of cancer (Oxford, England : 1990) 2023 5 188 81-89. Yiquan Xu, Jingjing Yan, Chengzhi Zhou, Lin Wu, Haibo Wang, Jun Zhao, Maolin Zhou, Jingyi Wang, Xinlong Zheng, Longfeng Zhang, Kan Jiang, Xiaobin Zheng, Qian Miao, Shiwen Wu, Zihua Zou, Rong Lian, Yuange He, Rongrong Chen, Shanshan Yang, Yujing Li, Sihui Chen, Gen L |
Whole-Exome Sequencing and cfDNA Analysis Uncover Genetic Determinants of Melanoma Therapy Response in a Real-World Setting. International journal of molecular sciences 2023 3 24 (5): . Vanni Irene, Pastorino Lorenza, Tanda Enrica Teresa, Andreotti Virginia, Dalmasso Bruna, Solari Nicola, Mascherini Matteo, Cabiddu Francesco, Guadagno Antonio, Coco Simona, Allavena Eleonora, Bruno William, Pietra Gabriella, Croce Michela, Gangemi Rosaria, Piana Michele, Zoppoli Gabriele, Ferrando Lorenzo, Spagnolo Francesco, Queirolo Paola, Ghiorzo Pao |
Characterisation and outcome of RAC1 mutated melanoma. European journal of cancer (Oxford, England : 1990) 2023 2 183 1-10. Lodde Georg C, Jansen Philipp, Herbst Rudolf, Terheyden Patrick, Utikal Jochen, Pföhler Claudia, Ulrich Jens, Kreuter Alexander, Mohr Peter, Gutzmer Ralf, Meier Friedegund, Dippel Edgar, Weichenthal Michael, Sucker Antje, Placke Jan-Malte, Zaremba Anne, Albrecht Lea Jessica, Kowall Bernd, Galetzka Wolfgang, Becker Jürgen C, Tasdogan Alpaslan, Zimmer Lisa, Livingstone Elisabeth, Hadaschik Eva, Schadendorf Dirk, Ugurel Selma, Griewank Kla |
Genetic profile of Chinese patients with small bowel cancer categorized by anatomic location. BMC medical genomics 2023 11 16 (1): 289. Chengmin Shi, Junrui Ma, Tong Zhang, Yanqiang Shi, Weiming Duan, Depei Huang, Hushan Zhang, Yujian Ze |
Association between Downstream Taste Signaling Genes, Oral Microbiome, and Severe Early Childhood Caries. International journal of molecular sciences 2023 1 24 (1): . de Jesus Vivianne Cruz, Mittermuller Betty-Anne, Hu Pingzhao, Schroth Robert J, Chelikani Prash |
Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivo. Molecular psychiatry 2023 1 . Bonnet Maxime, Roche Fiona, Fagotto-Kaufmann Christine, Gazdagh Gabriella, Truong Iona, Comunale Franck, Barbosa Sonia, Bonhomme Marion, Nafati Nicolas, Hunt David, Rodriguez Monserrat Pons, Chaudhry Ayeshah, Shears Deborah, Madruga Marcos, Vansenne Fleur, Curie Aurore, Kajava Andrey V, Baralle Diana, Fassier Coralie, Debant Anne, Schmidt Susan |
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- Page last updated:Apr 22, 2024
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