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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and PTPRO[original query]
Disruption of PTPRO causes childhood-onset nephrotic syndrome.
American journal of human genetics 2011 Jul 89 (1): 139-47.
Ozaltin Fatih, Ibsirlioglu Tulin, Taskiran Ekim Z, Baydar Dilek Ertoy, Kaymaz Figen, Buyukcelik Mithat, Kilic Beltinge Demircioglu, Balat Ayse, Iatropoulos Paraskevas, Asan Esin, Akarsu Nurten A, Schaefer Franz, Yilmaz Engin, Bakkaloglu Ay?in,
Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. GWAS Catalog
Journal of psychiatric research 2012 Feb 46 (2): 271-8.
LeBlanc Marissa, Kulle Bettina, Sundet Kjetil, Agartz Ingrid, Melle Ingrid, Djurovic Srdjan, Frigessi Arnoldo, Andreassen Ole
Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome.
Molecular biology reports 2021 Sep .
Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population.
Kidney international 2023 12 .
Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch
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