Simon DB - Search Results

1

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, Casari G, Bettinelli A, Colussi G, Rodriguez-Soriano J, McCredie D, Milford D, Sanjad S, Lifton RP. Simon DB, et al. Science. 1999 Jul 2;285(5424):103-6. doi: 10.1126/science.285.5424.103. Science. 1999. PMID: 10390358

2

Human hypertension caused by mutations in WNK kinases.

Wilson FH, Disse-Nicodème S, Choate KA, Ishikawa K, Nelson-Williams C, Desitter I, Gunel M, Milford DV, Lipkin GW, Achard JM, Feely MP, Dussol B, Berland Y, Unwin RJ, Mayan H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. Wilson FH, et al. Among authors: simon db. Science. 2001 Aug 10;293(5532):1107-12. doi: 10.1126/science.1062844. Science. 2001. PMID: 11498583

3

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.

Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA, Lifton RP. Simon DB, et al. Nat Genet. 1996 Jun;13(2):183-8. doi: 10.1038/ng0696-183. Nat Genet. 1996. PMID: 8640224

4

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP. Simon DB, et al. Nat Genet. 1996 Oct;14(2):152-6. doi: 10.1038/ng1096-152. Nat Genet. 1996. PMID: 8841184

5

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.

Simon DB, Lifton RP. Simon DB, et al. Am J Physiol. 1996 Nov;271(5 Pt 2):F961-6. doi: 10.1152/ajprenal.1996.271.5.F961. Am J Physiol. 1996. PMID: 8945989 Review.

6

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP. Simon DB, et al. Nat Genet. 1997 Oct;17(2):171-8. doi: 10.1038/ng1097-171. Nat Genet. 1997. PMID: 9326936

7

Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.

Simon DB, Lifton RP. Simon DB, et al. Adv Nephrol Necker Hosp. 1997;27:343-59. Adv Nephrol Necker Hosp. 1997. PMID: 9408455 Review. No abstract available.

8

Ion transporter mutations in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP. Simon DB, et al. Curr Opin Nephrol Hypertens. 1998 Jan;7(1):43-7. doi: 10.1097/00041552-199801000-00008. Curr Opin Nephrol Hypertens. 1998. PMID: 9442362 Review.

9

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP. Simon DB, et al. Curr Opin Cell Biol. 1998 Aug;10(4):450-4. doi: 10.1016/s0955-0674(98)80057-4. Curr Opin Cell Biol. 1998. PMID: 9719864 Review.

10

Mutations in the Na-Cl cotransporter reduce blood pressure in humans.

Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Gill JR, Lifton RP. Cruz DN, et al. Among authors: simon db. Hypertension. 2001 Jun;37(6):1458-64. doi: 10.1161/01.hyp.37.6.1458. Hypertension. 2001. PMID: 11408395

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