HuGE Literature Finder
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| Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study. Jornal de pediatria 2021 Oct . Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw |
| Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly. Viruses 2021 02 13 (2): . Gomes Julia A, Sgarioni Eduarda, Boquett Juliano A, Terças-Trettel Ana Cláudia P, da Silva Juliana H, Ribeiro Bethânia F R, Galera Marcial F, de Oliveira Thalita M, Carvalho de Andrade Maria Denise F, Carvalho Isabella F, Schüler-Faccini Lavínia, Vianna Fernanda S |
| Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes. Genes 2020 Nov 11 (12): . Balistreri Carmela Rita, Ammoscato Claudia Leonarda, Scola Letizia, Fragapane Tiziana, Giarratana Rosa Maria, Lio Domenico, Piccione Mar |
Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study.
The Lancet. Respiratory medicine 2020 Jan . Guillen-Guio Beatriz, Lorenzo-Salazar Jose M, Ma Shwu-Fan, Hou Pei-Chi, Hernandez-Beeftink Tamara, Corrales Almudena, García-Laorden M Isabel, Jou Jonathan, Espinosa Elena, Muriel Arturo, Domínguez David, Lorente Leonardo, Martín María M, Rodríguez-Gallego Carlos, Solé-Violán Jordi, Ambrós Alfonso, Carriedo Demetrio, Blanco Jesús, Añón José M, Reilly John P, Jones Tiffanie K, Ittner Caroline Ag, Feng Rui, Schöneweck Franziska, Kiehntopf Michael, Noth Imre, Scholz Markus, Brunkhorst Frank M, Scherag André, Meyer Nuala J, Villar Jesús, Flores Carl |
| Interaction between Vascular Endothelial Growth Factor-A (rs2010963) Gene Polymorphisms and Dietary Diversity Score on Cardiovascular Risk Factors in Patients with Metabolic Syndrome. Lifestyle genomics 2019 Nov 1-10. Abbasalizad Farhangi Mahdieh, Vajdi Mahdi, Nikniaz Leila, Nikniaz Zein |
| Analysis of VEGF gene polymorphisms and serum VEGF protein levels contribution in polycystic ovary syndrome of patients. Molecular biology reports 2019 Aug . Bao Lei, Syed Rabbani, Aloahd Mustafa Saws |
| Genetic and transcriptional landscape of plasma cells in POEMS syndrome. Leukemia 2019 Jan . Nagao Yuhei, Mimura Naoya, Takeda June, Yoshida Kenichi, Shiozawa Yusuke, Oshima Motohiko, Aoyama Kazumasa, Saraya Atsunori, Koide Shuhei, Rizq Ola, Hasegawa Yoshinori, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Nishijima Dai, Isshiki Yusuke, Kayamori Kensuke, Kawajiri-Manako Chika, Oshima-Hasegawa Nagisa, Tsukamoto Shokichi, Mitsukawa Shio, Takeda Yusuke, Ohwada Chikako, Takeuchi Masahiro, Iseki Tohru, Misawa Sonoko, Miyano Satoru, Ohara Osamu, Yokote Koutaro, Sakaida Emiko, Kuwabara Satoshi, Sanada Masashi, Iwama Atsushi, Ogawa Seishi, Nakaseko Chia |
| Vascular endothelial growth factor (VEGFA) gene variation in polycystic ovary syndrome in a Tunisian women population. BMC genomics 2016 Oct 17 (Suppl 9): 748. Ben Salem Assila, Megdich Fatma, Kacem Olfa, Souayeh Malek, Hachani Ben Ali Faten, Hizem Sondes, Janhai Faouzi, Ajina Mounir, Abu-Elmagd Muhammad, Assidi Mourad, Al Qahtani Mohammed H, Mahjoub Touha |
| Splenomegaly and Its Associations with Genetic Polymorphisms and Treatment Outcome in Colorectal Cancer Patients Treated with Adjuvant FOLFOX. Cancer research and treatment : official journal of Korean Cancer Association 2016 Jul 48 (3): 990-7. Kim Mi-Jung, Han Sae-Won, Lee Dae-Won, Cha Yongjun, Lee Kyung-Hun, Kim Tae-Yong, Oh Do-Youn, Kim Se Hyung, Im Seock-Ah, Bang Yung-Jue, Kim Tae-Y |
| Analysis of VEGFA Variants and Changes in VEGF Levels Underscores the Contribution of VEGF to Polycystic Ovary Syndrome. PloS one 2016 11 (11): e0165636. Almawi Wassim Y, Gammoh Emily, Malalla Zainab H, Al-Madhi Safa |
| Identification of gene variants related to the nitric oxide pathway in patients with acute coronary syndrome. Gene 2015 Jul . Umman B, Cakmakoglu B, Cincin Z B, Kocaaga M, Emet S, Tamer S, Gokkusu |
| Interleukin and growth factor gene variants and risk of carpal tunnel syndrome. Gene 2015 Jun 564 (1): 67-72. Burger Marilize C, de Wet Hanli, Collins Malco |
| Identification of gene variants associated with hypoxia pathway in acute coronary syndrome: a pilot study. Molecular biology reports 2014 Dec 41 (12): 8055-61. Gokkusu Cahide, Cakmakoglu Bedia, Cincin Zeynep Birsu, Karaagac Mehmet, Emet Samim, Tamer Sule, Umman Berr |
| Impact of VEGFA -583C?>?T polymorphism on serum VEGF levels and the susceptibility to acute chest syndrome in pediatric patients with sickle cell disease. Pediatric blood & cancer 2014 Dec 61 (12): 2310-2. Redha Noor A, Mahdi Najat, Al-Habboubi Hebah H, Almawi Wassim |
| CYP1A1, GCLC, AGT, AGTR1 gene-gene interactions in community-acquired pneumonia pulmonary complications. Molecular biology reports 2013 Nov 40 (11): 6163-76. Salnikova Lyubov E, Smelaya Tamara V, Golubev Arkadiy M, Rubanovich Alexander V, Moroz Viktor |
| The outcome and predictive factors of sunitinib therapy in advanced gastrointestinal stromal tumors (GIST) after imatinib failure - one institution study. BMC cancer 2012 12 (1): 107. Rutkowski Piotr, Bylina El?bieta, Klimczak Anna, Switaj Tomasz, Falkowski S?awomir, Kroc Jacek, Lugowska Iwona, Brzeskwiniewicz Magdalena, Melerowicz Wojciech, Osuch Czes?aw, Mierzejewska Ewa, Wasielewski Kacper, Wo?niak Agnieszka, Grzesiakowska Urszula, Nowecki Zbigniew I, Siedlecki Janusz A, Limon Janu |
| VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study. Biological research 2009 42 (4): 461-8. Calderón Juan Francisco, Puga Alonso R, Guzmán M Luisa, Astete Carmen Paz, Arriaza Marta, Aracena Mariana, Aravena Teresa, Sanz Patricia, Repetto Gabriela |
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- Page last updated:Jun 27, 2022
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