Hyperaldosteronism research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Hyperaldosteronism treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 20 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
Biosynthesis of the major zona pellucida glycoprotein secreted by oocytes during mammalian oogenesis.
Greve J M, Salzmann G S, Roller R J, Wassarman P M
Cell Vol 31(3 Pt 2)
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Date 01 Dec 1982
Research
The neuroendocrine protein 7B2 is required for peptide hormone processing in vivo and provides a novel mechanism for pituitary Cushing's disease.
Westphal C H, Muller L, Zhou A, Zhu X, Bonner-Weir S ...
Cell Vol 96(5)
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Date 05 Mar 1999
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Retinal ligatin recognizes glycoproteins bearing oligosaccharides terminating in phosphodiester-linked glucose.
Marchase R B, Koro L A, Kelly C M, McClay D R
Cell Vol 28(4)
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Date 01 Apr 1982
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Impaired intracellular transport of class I MHC antigens as a possible means for adenoviruses to evade immune surveillance.
Andersson M, Pääbo S, Nilsson T, Peterson P A
Cell Vol 43(1)
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Date 01 Nov 1985
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Biosynthesis of the IgA antibody receptor: a model for the transepithelial sorting of a membrane glycoprotein.
Solari R, Kraehenbuhl J P
Cell Vol 36(1)
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Date 01 Jan 1984
Research
Conformation-independent binding of monoglucosylated ribonuclease B to calnexin.
Zapun A, Petrescu S M, Rudd P M, Dwek R A, Thomas D Y ...
Cell Vol 88(1)
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Date 10 Jan 1997
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Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel.
Shimkets R A, Warnock D G, Bositis C M, Nelson-Williams C, Hansson J H ...
Cell Vol 79(3)
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Date 04 Nov 1994
Research
Three types of muscle-specific gene expression in fusion-blocked rat skeletal muscle cells: translational control in EGTA-treated cells.
Endo T, Nadal-Ginard B
Cell Vol 49(4)
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Date 22 May 1987
Research
Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.
Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y ...
Cell Vol 73(4)
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Date 21 May 1993
Research
Identification of regions of the SV40 genome which contain preferred SV40 T antigen-binding sites.
Jessel D, Landau T, Hudson J, Lalor T, Tenen D ...
Cell Vol 8(4)
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Date 01 Aug 1976
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