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166 results
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Getting a foothold in nephrotic syndrome.
Somlo S, Mundel P. Somlo S, et al. Nat Genet. 2000 Apr;24(4):333-5. doi: 10.1038/74139. Nat Genet. 2000. PMID: 10742089 No abstract available.
Mutations in SEC63 cause autosomal dominant polycystic liver disease.
Davila S, Furu L, Gharavi AG, Tian X, Onoe T, Qian Q, Li A, Cai Y, Kamath PS, King BF, Azurmendi PJ, Tahvanainen P, Kääriäinen H, Höckerstedt K, Devuyst O, Pirson Y, Martin RS, Lifton RP, Tahvanainen E, Torres VE, Somlo S. Davila S, et al. Among authors: somlo s. Nat Genet. 2004 Jun;36(6):575-7. doi: 10.1038/ng1357. Epub 2004 May 9. Nat Genet. 2004. PMID: 15133510
PKD1 interacts with PKD2 through a probable coiled-coil domain.
Qian F, Germino FJ, Cai Y, Zhang X, Somlo S, Germino GG. Qian F, et al. Among authors: somlo s. Nat Genet. 1997 Jun;16(2):179-83. doi: 10.1038/ng0697-179. Nat Genet. 1997. PMID: 9171830
Signal transduction. Mating, channels and kidney cysts.
Emmons SW, Somlo S. Emmons SW, et al. Among authors: somlo s. Nature. 1999 Sep 23;401(6751):339-40. doi: 10.1038/43810. Nature. 1999. PMID: 10517627 No abstract available.
Cardiac defects and renal failure in mice with targeted mutations in Pkd2.
Wu G, Markowitz GS, Li L, D'Agati VD, Factor SM, Geng L, Tibara S, Tuchman J, Cai Y, Park JH, van Adelsberg J, Hou H Jr, Kucherlapati R, Edelmann W, Somlo S. Wu G, et al. Among authors: somlo s. Nat Genet. 2000 Jan;24(1):75-8. doi: 10.1038/71724. Nat Genet. 2000. PMID: 10615132
A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation.
Fedeles SV, Tian X, Gallagher AR, Mitobe M, Nishio S, Lee SH, Cai Y, Geng L, Crews CM, Somlo S. Fedeles SV, et al. Among authors: somlo s. Nat Genet. 2011 Jun 19;43(7):639-47. doi: 10.1038/ng.860. Nat Genet. 2011. PMID: 21685914 Free PMC article.
Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease.
Ma M, Tian X, Igarashi P, Pazour GJ, Somlo S. Ma M, et al. Among authors: somlo s. Nat Genet. 2013 Sep;45(9):1004-12. doi: 10.1038/ng.2715. Epub 2013 Jul 28. Nat Genet. 2013. PMID: 23892607 Free PMC article.
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).
Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnik-Schöneborn S, Furu L, Onuchic LF, De Baca M, Germino GG, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K. Bergmann C, et al. Among authors: somlo s. J Am Soc Nephrol. 2003 Jan;14(1):76-89. doi: 10.1097/01.asn.0000039578.55705.6e. J Am Soc Nephrol. 2003. PMID: 12506140
Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene.
Nagasawa Y, Matthiesen S, Onuchic LF, Hou X, Bergmann C, Esquivel E, Senderek J, Ren Z, Zeltner R, Furu L, Avner E, Moser M, Somlo S, Guay-Woodford L, Büttner R, Zerres K, Germino GG. Nagasawa Y, et al. Among authors: somlo s. J Am Soc Nephrol. 2002 Sep;13(9):2246-58. doi: 10.1097/01.asn.0000030392.19694.9d. J Am Soc Nephrol. 2002. PMID: 12191969
TREX1 Mutation Causing Autosomal Dominant Thrombotic Microangiopathy and CKD-A Novel Presentation.
Gulati A, Bale AE, Dykas DJ, Bia MJ, Danovitch GM, Moeckel GW, Somlo S, Dahl NK. Gulati A, et al. Among authors: somlo s. Am J Kidney Dis. 2018 Dec;72(6):895-899. doi: 10.1053/j.ajkd.2018.05.006. Epub 2018 Jun 22. Am J Kidney Dis. 2018. PMID: 29941221 Review.
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