Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Disease and GDNF[original query] |
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| Gdnf haploinsufficiency causes Hirschsprung-like intestinal obstruction and early-onset lethality in mice. American journal of human genetics 2002 1 70 (2): 435-47. Shen Liya, Pichel José G, Mayeli Thomas, Sariola Hannu, Lu Bai, Westphal Hein |
| Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients. Journal of human genetics 2006 51 (12): 1126-32. Sangkhathat Surasak, Kusafuka Takeshi, Chengkriwate Piyawan, Patrapinyokul Sakda, Sangthong Burapat, Fukuzawa Masahi |
| Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany. Neurobiology of aging 2010 Jan 31 (1): 167-8. Lücking C B, Lichtner P, Kramer E R, Gieger C, Illig T, Dichgans M, Berg D, Gasser |
| A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung disease. Annals of human genetics 2009 Jan 73 (1): 19-25. Fernández R M, Sánchez-Mejías A, Mena M D, Ruiz-Ferrer M, López-Alonso M, Antiñolo G, Borrego |
| Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung disease. Journal of pediatric surgery 2008 Nov 43 (11): 2042-7. Fernandez Raquel M, Ruiz-Ferrer Macarena, Lopez-Alonso Manuel, Antiñolo Guillermo, Borrego Sal |
| Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic association. Medicine 2009 Mar 88 (2): 83-90. Pini Prato Alessio, Musso Marco, Ceccherini Isabella, Mattioli Girolamo, Giunta Camilla, Ghiggeri Gian Marco, Jasonni Vincen |
| A candidate gene study of obstructive sleep apnea in European Americans and African Americans. American journal of respiratory and critical care medicine 2010 Oct 182 (7): 947-53. Larkin Emma K, Patel Sanjay R, Goodloe Robert J, Li Yali, Zhu Xiaofeng, Gray-McGuire Courtney, Adams Mark D, Redline Sus |
| Glial cell line-derived neurotrophic factor receptor alpha 2 (GFRA2) gene is associated with tardive dyskinesia. Psychopharmacology 2010 Jun 210 (3): 347-54. Souza Renan P, de Luca Vincenzo, Remington Gary, Lieberman Jeffrey A, Meltzer Herbert Y, Kennedy James L, Wong Albert H |
| Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population. Progress in neuro-psychopharmacology & biological psychiatry 2011 Jul 35 (5): 1268-72. Yoshimura Tomoko, Usui Hinako, Takahashi Nagahide, Yoshimi Akira, Saito Shinichi, Aleksic Branko, Ujike Hiroshi, Inada Toshiya, Yamada Mitsuhiko, Uchimura Naohisa, Iwata Nakao, Sora Ichiro, Iyo Masaomi, Ozaki Nor |
| RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. Journal of medical genetics 2011 Jul 48 (7): 497-504. Jeanpierre Cécile, Macé Guillaume, Parisot Mélanie, Morinière Vincent, Pawtowsky Audrey, Benabou Marion, Martinovic Jelena, Amiel Jeanne, Attié-Bitach Tania, Delezoide Anne-Lise, Loget Philippe, Blanchet Patricia, Gaillard Dominique, Gonzales Marie, Carpentier Wassila, Nitschke Patrick, Tores Frédéric, Heidet Laurence, Antignac Corinne, Salomon Rémi, |
| Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease. Neuroscience letters 2011 Apr 493 (3): 97-101. Choi Jung-Mi, Hong Jung-Hoon, Chae Min-Joo, Ngyuen Phuoc Hung, Kang Hyun-Sook, Ma Hyeo-Il, Kim Yun Joo |
| RET and NRG1 interplay in Hirschsprung disease. Human genetics 2013 May 132 (5): 591-600. Gui Hongsheng, Tang Wai-Kiu, So Man-Ting, Proitsi Petroola, Sham Pak C, Tam Paul K, Ngan Elly Sau-Wai, Sau-Wai Ngan Elly, Cherny Stacey S, Garcia-Barceló Maria-Mer |
| Glial cell line-derived neurotrophic factor (GDNF) as a novel candidate gene of anxiety. PloS one 2013 8 (12): e80613. Kotyuk Eszter, Keszler Gergely, Nemeth Nora, Ronai Zsolt, Sasvari-Szekely Maria, Szekely An |
Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD.
The European respiratory journal 2015 Jan 45 (1): 60-75. Dijkstra Akkelies E, Boezen H Marike, van den Berge Maarten, Vonk Judith M, Hiemstra Pieter S, Barr R Graham, Burkart Kirsten M, Manichaikul Ani, Pottinger Tess D, Silverman Edward K, Cho Michael H, Crapo James D, Beaty Terri H, Bakke Per, Gulsvik Amund, Lomas David A, Bossé Yohan, Nickle David C, Paré Peter D, de Koning Harry J, Lammers Jan-Willem, Zanen Pieter, Smolonska Joanna, Wijmenga Ciska, Brandsma Corry-Anke, Groen Harry J M, Postma Dirkje S, |
| Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrb(sl) mutations. Gene 2015 Aug . Huang Jieping, Dang Ruihua, Torigoe Daisuke, Li Anqi, Lei Chuzhao, Sasaki Nobuya, Wang Jinxi, Agui Takas |
| Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis. PloS one 2015 10 (3): e0122068. Huang Jieping, Dang Ruihua, Torigoe Daisuke, Lei Chuzhao, Lan Xianyong, Chen Hong, Sasaki Nobuya, Wang Jinxi, Agui Takas |
| Relationship Between Chronic Tinnitus and Glial Cell Line-Derived Neurotrophic Factor Gene rs3812047, rs1110149, and rs884344 Polymorphisms in a Turkish Population. Biochemical genetics 2016 Aug 54 (4): 552-563. Orenay-Boyacioglu Seda, Coskunoglu Aysun, Caki Zerrin, Cam Fethi Sir |
| Association Between RET (rs1800860) and GFRA1 (rs45568534, rs8192663, rs181595401, rs7090693, and rs2694770) Variants and Kidney Size in Healthy Newborns. Genetic testing and molecular biomarkers 2016 Oct 20 (10): 624-628. Kaczmarczyk Mariusz, Loniewska Beata, Kuprjanowicz Anna, Binczak-Kuleta Agnieszka, Goracy Iwona, Ryder Malgorzata, Taryma-Lesniak Olga, Ciechanowicz Andrz |
| Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism. BMC urology 2017 12 17 (1): 112. Mizuno Kentaro, Nakane Akihiro, Nishio Hidenori, Moritoki Yoshinobu, Kamisawa Hideyuki, Kurokawa Satoshi, Kato Taiki, Ando Ryosuke, Maruyama Tetsuji, Yasui Takahiro, Hayashi Yuta |
| Serum protein pattern associated with organ damage and lupus nephritis in systemic lupus erythematosus revealed by PEA immunoassay. Clinical proteomics 2017 10 14 32. Petrackova Anna, Smrzova Andrea, Gajdos Petr, Schubertova Marketa, Schneiderova Petra, Kromer Pavel, Snasel Vaclav, Skacelova Martina, Mrazek Frantisek, Zadrazil Josef, Horak Pavel, Kriegova E |
| Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
| Chronic tinnitus and BDNF/GDNF CpG promoter methylations: a case-control study. Molecular biology reports 2019 Apr . Orenay-Boyacioglu Seda, Caliskan Metin, Boyacioglu Olcay, Coskunoglu Aysun, Bozkurt Gokay, Cam F Sir |
| Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival. EBioMedicine 2019 Jan . Hallberg Pär, Smedje Hans, Eriksson Niclas, Kohnke Hugo, Daniilidou Makrina, Öhman Inger, Yue Qun-Ying, Cavalli Marco, Wadelius Claes, Magnusson Patrik K E, Landtblom Anne-Marie, Wadelius Mia, |
| Glial Cell-Derived Neurotrophic Factor Functions as a Potential Candidate Gene in Obstructive Sleep Apnea Based on a Combination of Bioinformatics and Targeted Capture Sequencing Analyses. BioMed research international 2021 3 2021 6656943. Cao Yuanyuan, Zhu Qing, Cai Xintian, Wu Ting, Aierken Xiayire, Ahmat Ayguzal, Liu Shasha, Li Nanfa |
| Evaluation of the relationship between SORL1 gene polymorphism and Parkinson's disease in the Chinese population. Neuroscience letters 2022 4 778 136602. Wang Ying, Luan Mengting, Xue Li, Jin Jianing, Xie An |
| Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease. Journal of pediatric surgery 2022 12 . Gunadi , Kalim Alvin Santoso, Iskandar Kristy, Marcellus , Puspitarani Dyah Ayu, Diposarosa Rizki, Makhmudi Akhmad, Astuti Galuh Dyah N |
| MicroRNA-Mediated Suppression of Glial Cell Line-Derived Neurotrophic Factor Expression Is Modulated by a Schizophrenia-Associated Non-Coding Polymorphism. International journal of molecular sciences 2024 4 25 (8): . Gergely Keszler, Bálint Vékony, Zsuzsanna Elek, Zsófia Nemoda, Nóra Angyal, Zsófia Bánlaki, Réka Kovács-Nagy, Zsolt Rónai, János M Réthel |
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