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Proceedings of the National Academy of Sciences of the United States of America|October 11, 2013
Ligand-specific conformational change of the G-protein-coupled receptor ALX/FPR2 determines proresolving functional responsesSadani N Cooray, Thomas Gobbetti, Trinidad Montero-Melendez, et al.
Molecular Endocrinology (Baltimore, Md.)|October 27, 2009
Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanismHelen L Storr, Barbara Kind, David A Parfitt, et al.
Clinical Endocrinology|August 31, 2002
Spontaneous growth hormone secretory characteristics in children with partial growth hormone insensitivityRagnar Bjarnason, Kausik Banerjee, Steven J Rose, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 8, 2018
MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonationTatiana V Novoselova, Mashal Hussain, Peter J King, et al.
Molecular Endocrinology (Baltimore, Md.)|October 3, 2013
Melanocortin 4 receptor becomes an ACTH receptor by coexpression of melanocortin receptor accessory protein 2Maria Josep Agulleiro, Raúl Cortés, Begoña Fernández-Durán, et al.
Human Genetics|October 18, 2002
Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneityEmmanuelle Génin, Angela Huebner, Christine Jaillard, et al.
Endocrine Reviews|April 29, 2011
Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivityAlessia David, Vivian Hwa, Louise A Metherell, et al.
Molecular Neurodegeneration|May 4, 2023
Opinion: more mouse models and more translation needed for ALSElizabeth M C Fisher, Linda Greensmith, Andrea Malaspina, et al.
Molecular Endocrinology (Baltimore, Md.)|November 29, 2002
Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activityFrancesca M Swords, Asma Baig, Diana M Malchoff, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2012
Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndromeRenuka P Dias, Irina Bogdarina, Jean-Baptiste Cazier, et al.
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