Salt handling and hypertension

von O’Shaughnessy, Kevin M., Karet, Fiona E.
Veröffentlicht 2004

Targeting the renin-angiotensin system in patients with renal disease

von Devonald, Mark A J, Karet, Fiona E
Veröffentlicht 2002

An Extended Nomenclature for Mammalian V-ATPase Subunit Genes and Splice Variants

von Miranda, Kevin C., Karet, Fiona E., Brown, Dennis
Veröffentlicht 2010

The d subunit plays a central role in human vacuolar H(+)-ATPases

von Smith, Annabel N., Francis, Richard W., Sorrell, Sara L., Karet, Fiona E.
Veröffentlicht 2008

Uromodulin Exclusion List Improves Urinary Exosomal Protein Identification

von Hiemstra, Thomas F., Charles, Philip D., Hester, Svenja S., Karet, Fiona E., Lilley, Kathryn S.
Veröffentlicht 2011

Importance of early audiologic assessment in distal renal tubular acidosis

von Swayamprakasam, Anand P, Stover, Elizabeth, Norgett, Elizabeth, Blake-Palmer, Katherine G, Cunningham, Michael J, Karet, Fiona E
Veröffentlicht 2010

RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels

von Brown, Alice C. N., Hallouane, Dalila, Mawby, William J., Karet, Fiona E., Saleem, Moin A., Howie, Alexander J., Toye, Ashley M.
Veröffentlicht 2009

Human H(+)ATPase a4 subunit mutations causing renal tubular acidosis reveal a role for interaction with phosphofructokinase-1

von Su, Ya, Blake-Palmer, Katherine G., Sorrell, Sara, Javid, Babak, Bowers, Katherine, Zhou, Aiwu, Chang, Simon H., Qamar, Seema, Karet, Fiona E.
Veröffentlicht 2008

Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing (rdRTA2) to 7q33-34

von Karet, Fiona E., Finberg, Karin E., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Medina, Juan F., Lifton, Richard P.
Veröffentlicht 1999

Glyceraldehyde 3-phosphate dehydrogenase is required for band 3 (anion exchanger 1) membrane residency in the mammalian kidney

von Su, Ya, Blake-Palmer, Katherine G., Fry, Andrew C., Best, Alison, Brown, Alice C. N., Hiemstra, Thomas F., Horita, Shoko, Zhou, Aiwu, Toye, Ashley M., Karet, Fiona E.
Veröffentlicht 2011

Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum

von Williams, Siân E., Reed, Anita A.C., Galvanovskis, Juris, Antignac, Corinne, Goodship, Tim, Karet, Fiona E., Kotanko, Peter, Lhotta, Karl, Morinière, Vincent, Williams, Paul, Wong, William, Rorsman, Patrik, Thakker, Rajesh V.
Veröffentlicht 2009

SAT-224 Recurrent Co-Driver Mutation in CTNNB1-Mutant Aldosterone-producing Adenomas (APA), Causing Reversible Hypertension in Puberty, Pregnancy or Menopause

von Zhou, Junhua, Cabrera, Claudia P, Azizan, Elena A B, Fernandes-Rosa, Fabio, Cottrell, Emily, Amar, Laurence, Argentesi, Giulia, Wu, Xilin, Marker, Alison, Jordan, Suzanne, Polubothu, Satyamaanasa, Berney, Daniel M, Tuthill, Antoinette, Karet, Fiona E, Metherell, Louise, Teo, Ada, Thakker, Rajesh V, Drake, William, Boulkroun, Sheerazed, Kinsler, Veronica, Storr, Helen Louise, Zennaro, Maria-Christina, Brown, Morris Jonathan
Veröffentlicht in J Endocr Soc (2020)

Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities

von Boyden, Lynn M., Choi, Murim, Choate, Keith A., Nelson-Williams, Carol J., Farhi, Anita, Toka, Hakan R., Tikhonova, Irina R., Bjornson, Robert, Mane, Shrikant M., Colussi, Giacomo, Lebel, Marcel, Gordon, Richard D., Semmekrot, Ben A., Poujol, Alain, Välimäki, Matti J., De Ferrari, Maria E., Sanjad, Sami A., Gutkin, Michael, Karet, Fiona E., Tucci, Joseph R., Stockigt, Jim R., Keppler-Noreuil, Kim M., Porter, Craig C., Anand, Sudhir K., Whiteford, Margo L., Davis, Ira D., Dewar, Stephanie B., Bettinelli, Alberto, Fadrowski, Jeffrey J., Belsha, Craig W., Hunley, Tracy E., Nelson, Raoul D., Trachtman, Howard, Cole, Trevor R. P., Pinsk, Maury, Bockenhauer, Detlef, Shenoy, Mohan, Vaidyanathan, Priya, Foreman, John W., Rasoulpour, Majid, Thameem, Farook, Al-Shahrouri, Hania Z., Radhakrishnan, Jai, Gharavi, Ali G., Goilav, Beatrice, Lifton, Richard P.
Veröffentlicht 2012