Wolf K45E Manuel d'utilisateur Page 117

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Literaturverzeichnis
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110
Guay-Woodford LM
Bartter syndrome: Unraveling the pathophysiologic enigma
Am. J. Med. 105: 151-161, 1998
Hebert SC, Friedman P, Andreoli TE
The effects of antidiuretic hormone on cellular conductive pathways in mouse medullary thick
ascending limbs of Henle. I. ADH increases transcellular conductance pathways
J. Membrane Biol. 80: 201-219, 1984
Hensen P
Molekulare Genetik der hereditären hypokaliämischen Tubulopathien
Inaugural-Dissertation: 1-108, 1999
Heukeshoven J, Dernick R
Simplified method for silver staining of proteins in polyacrylamide gels and the mechanism of
silver staining
Electrophoresis 6: 103-112, 1985
Ho K, Nichols CG, Lederer WJ, Lytton J, Vassilev PM, Kanazirska MV, Hebert SC
Cloning and expression of an inwardly rectifying ATP-regulated potassium channel
Nature 362: 31-37, 1993
Hunter M
Ion channels: Accessory to kidney disease
Nature 414: 502-503, 2001
International Collaborative Study Group for Bartter-like syndromes (ICSBS), consisting of:
Károlyi L, Konrad M, Köckerling A, Ziegler A, Zimmermann DK, Roth B. Wieg C, Grzeschik KH,
Koch MC, Seyberth HW, Vargas R, Forestier L, Jean G, Deschaux M, Rizzoni GF, Niaudet P,
Antignac C, Feldmann D, Lorridon F, Cougoureux E, Laroze F, Alessandri JL, David L, Saunier
P, Deschênes G, Hildebrandt F, Vollmer M, Proesmans W, Brandis M, Heuvel LPWJ van den,
Lemmink HH, Nillesen W, Monnens LAH, Knoers NVAM, Guay-Woodford LM, Wright CJ,
Madrigal G, Hebert SC
Mutations in the gene encoding the inwardly-rectifying rebal potassium channel, ROMK, cause
the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity
Hum. Mol. Gen. 6, No 1: 17-26, 1997
Isomoto S, Chikako K, Kurachi Y
Inwardly rectifying potassium channels: Their molecular heterogeneity and function
Jap. J. Physiol. 47: 11-39, 1997
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