Finberg K - Search Results

1

Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae.

Burns N, Grimwade B, Ross-Macdonald PB, Choi EY, Finberg K, Roeder GS, Snyder M. Burns N, et al. Among authors: finberg k. Genes Dev. 1994 May 1;8(9):1087-105. doi: 10.1101/gad.8.9.1087. Genes Dev. 1994. PMID: 7926789 Free article.

2

Genetic heterogeneity of inherited cerebral cavernous malformation.

Günel M, Awad IA, Finberg K, Steinberg GK, Craig HD, Cepeda O, Nelson-Williams C, Lifton RP. Günel M, et al. Among authors: finberg k. Neurosurgery. 1996 Jun;38(6):1265-71. doi: 10.1097/00006123-199606000-00059. Neurosurgery. 1996. PMID: 8727164

3

Molecular cloning and characterization of Atp6v1b1, the murine vacuolar H+ -ATPase B1-subunit.

Finberg KE, Wagner CA, Stehberger PA, Geibel JP, Lifton RP. Finberg KE, et al. Gene. 2003 Oct 30;318:25-34. doi: 10.1016/s0378-1119(03)00790-x. Gene. 2003. PMID: 14585495

4

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.

Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP. Karet FE, et al. Among authors: finberg ke. Nat Genet. 1999 Jan;21(1):84-90. doi: 10.1038/5022. Nat Genet. 1999. PMID: 9916796

5

Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis.

Stehberger PA, Schulz N, Finberg KE, Karet FE, Giebisch G, Lifton RP, Geibel JP, Wagner CA. Stehberger PA, et al. J Am Soc Nephrol. 2003 Dec;14(12):3027-38. doi: 10.1097/01.asn.0000099375.74789.ab. J Am Soc Nephrol. 2003. PMID: 14638902

6

A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans.

Gunel M, Awad IA, Finberg K, Anson JA, Steinberg GK, Batjer HH, Kopitnik TA, Morrison L, Giannotta SL, Nelson-Williams C, Lifton RP. Gunel M, et al. Among authors: finberg k. N Engl J Med. 1996 Apr 11;334(15):946-51. doi: 10.1056/NEJM199604113341503. N Engl J Med. 1996. PMID: 8596595 Free article.

7

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.

Karet FE, Finberg KE, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Medina JF, Lifton RP. Karet FE, et al. Among authors: finberg ke. Am J Hum Genet. 1999 Dec;65(6):1656-65. doi: 10.1086/302679. Am J Hum Genet. 1999. PMID: 10577919 Free PMC article.

8

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: finberg k. Hypertension. 2001 Jun;37(6):1458-64. doi: 10.1161/01.hyp.37.6.1458. Hypertension. 2001. PMID: 11408395

9

Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene.

Smith AN, Finberg KE, Wagner CA, Lifton RP, Devonald MA, Su Y, Karet FE. Smith AN, et al. Among authors: finberg ke. J Biol Chem. 2001 Nov 9;276(45):42382-8. doi: 10.1074/jbc.M107267200. Epub 2001 Aug 8. J Biol Chem. 2001. PMID: 11495928 Free article.

10

Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status.

Wagner CA, Finberg KE, Stehberger PA, Lifton RP, Giebisch GH, Aronson PS, Geibel JP. Wagner CA, et al. Kidney Int. 2002 Dec;62(6):2109-17. doi: 10.1046/j.1523-1755.2002.00671.x. Kidney Int. 2002. PMID: 12427135 Free article.

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