Human Genome Epidemiology Literature Finder
|
Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and ADD2[original query] |
|---|
| Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008 Sep 29 (6): 824-8. Teggi Roberto, Lanzani Chiara, Zagato Laura, Delli Carpini Simona, Manunta Paolo, Bianchi Giuseppe, Bussi Mar |
| Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites. BMC medical genomics 2008 1 (1): 16. Kardia Sharon Lr, Greene M Todd, Boerwinkle Eric, Turner Stephen T, Kullo Iftikhar |
| alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy. Journal of molecular medicine (Berlin, Germany) 2010 Feb 88 (2): 203-17. Ferrandi Mara, Cusi Daniele, Molinari Isabella, Del Vecchio Lucia, Barlassina Cristina, Rastaldi Maria Pia, Schena Francesco Paolo, Macciardi Fabio, Marcantoni Carmelita, Roccatello Dario, Peters Luanne L, Armelloni Silvia, Min Li, Giardino Laura, Mattinzoli Deborah, Camisasca Claudio, Palazzo Fiorentina, Manunta Paolo, Ferrari Patrizia, Bianchi Giusep |
| [Association and interaction of AGT, AGTR1, ACE, ADRB2, DRD1, ADD1, ADD2, ATP2B1, TBXA2R and PTGS2 genes on the risk of hypertension in Antioquian population]. Biomédica : revista del Instituto Nacional de Salud 0 33 (4): 598-614. Valencia Diana María, Naranjo Carlos Andrés, Parra María Victoria, Caro María Antonieta, Valencia Ana Victoria, Jaramillo Carlos José, Bedoya Gabri |
- Page last reviewed:Feb 1, 2024
- Content source: