Somlo S - Search Results

1

Somatic inactivation of Pkd2 results in polycystic kidney disease.

Wu G, D'Agati V, Cai Y, Markowitz G, Park JH, Reynolds DM, Maeda Y, Le TC, Hou H Jr, Kucherlapati R, Edelmann W, Somlo S. Wu G, et al. Among authors: somlo s. Cell. 1998 Apr 17;93(2):177-88. doi: 10.1016/s0092-8674(00)81570-6. Cell. 1998. PMID: 9568711 Free article.

2

Evidence for a third genetic locus for autosomal dominant polycystic kidney disease.

Daoust MC, Reynolds DM, Bichet DG, Somlo S. Daoust MC, et al. Among authors: somlo s. Genomics. 1995 Feb 10;25(3):733-6. doi: 10.1016/0888-7543(95)80020-m. Genomics. 1995. PMID: 7759112

3

A kindred exhibiting cosegregation of an overlap connective tissue disorder and the chromosome 16 linked form of autosomal dominant polycystic kidney disease.

Somlo S, Rutecki G, Giuffra LA, Reeders ST, Cugino A, Whittier FC. Somlo S, et al. J Am Soc Nephrol. 1993 Dec;4(6):1371-8. doi: 10.1681/ASN.V461371. J Am Soc Nephrol. 1993. PMID: 8130364

4

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein.

Mochizuki T, Wu G, Hayashi T, Xenophontos SL, Veldhuisen B, Saris JJ, Reynolds DM, Cai Y, Gabow PA, Pierides A, Kimberling WJ, Breuning MH, Deltas CC, Peters DJ, Somlo S. Mochizuki T, et al. Among authors: somlo s. Science. 1996 May 31;272(5266):1339-42. doi: 10.1126/science.272.5266.1339. Science. 1996. PMID: 8650545

5

An integrated genetic and physical map of the autosomal recessive polycystic kidney disease region.

Lens XM, Onuchic LF, Wu G, Hayashi T, Daoust M, Mochizuki T, Santarina LB, Stockwin JM, Mücher G, Becker J, Sweeny WE Jr, Avner ED, Guay-Woodford L, Zerres K, Somlo S, Germino GG. Lens XM, et al. Among authors: somlo s. Genomics. 1997 May 1;41(3):463-6. doi: 10.1006/geno.1997.4671. Genomics. 1997. PMID: 9169147 Free article.

6

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

7

Characterization of the exon structure of the polycystic kidney disease 2 gene (PKD2).

Hayashi T, Mochizuki T, Reynolds DM, Wu G, Cai Y, Somlo S. Hayashi T, et al. Among authors: somlo s. Genomics. 1997 Aug 15;44(1):131-6. doi: 10.1006/geno.1997.4851. Genomics. 1997. PMID: 9286709

8

A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).

Veldhuisen B, Saris JJ, de Haij S, Hayashi T, Reynolds DM, Mochizuki T, Elles R, Fossdal R, Bogdanova N, van Dijk MA, Coto E, Ravine D, Nørby S, Verellen-Dumoulin C, Breuning MH, Somlo S, Peters DJ. Veldhuisen B, et al. Among authors: somlo s. Am J Hum Genet. 1997 Sep;61(3):547-55. doi: 10.1086/515497. Am J Hum Genet. 1997. PMID: 9326320 Free PMC article.

9

Molecular cloning, cDNA sequence analysis, and chromosomal localization of mouse Pkd2.

Wu G, Mochizuki T, Le TC, Cai Y, Hayashi T, Reynolds DM, Somlo S. Wu G, et al. Among authors: somlo s. Genomics. 1997 Oct 1;45(1):220-3. doi: 10.1006/geno.1997.4920. Genomics. 1997. PMID: 9339380

10

Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene.

Viribay M, Hayashi T, Tellería D, Mochizuki T, Reynolds DM, Alonso R, Lens XM, Moreno F, Harris PC, Somlo S, San Millán JL. Viribay M, et al. Among authors: somlo s. Hum Genet. 1997 Dec;101(2):229-34. doi: 10.1007/s004390050621. Hum Genet. 1997. PMID: 9402976

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