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Background publications
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Domingues, Font, Sobrinho, Bugalho: "A novel variant in Serpina7 gene in a family with thyroxine-binding globulin deficiency." in: Endocrine, Vol. 36, Issue 1, pp. 83-6, 2009 (PubMed).
Lacka, Nizankowska, Ogrodowicz, Lacki: "A novel mutation (del 1711 G) in the TBG gene as a cause of complete TBG deficiency." in: Thyroid : official journal of the American Thyroid Association, Vol. 17, Issue 11, pp. 1143-6, 2007 (PubMed).
Liu, Qian, Gritsenko, Camp, Monroe, Moore, Smith: "Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry." in: Journal of proteome research, Vol. 4, Issue 6, pp. 2070-80, 2005 (PubMed).
Ross, Grafham, Coffey, Scherer, McLay, Muzny, Platzer, Howell, Burrows, Bird, Frankish, Lovell, Howe, Ashurst, Fulton, Sudbrak, Wen, Jones, Hurles, Andrews, Scott, Searle, Ramser, Whittaker, Deadman et al.: "The DNA sequence of the human X chromosome. ..." in: Nature, Vol. 434, Issue 7031, pp. 325-37, 2005 (PubMed).
Anderson, Polanski, Pieper, Gatlin, Tirumalai, Conrads, Veenstra, Adkins, Pounds, Fagan, Lobley: "The human plasma proteome: a nonredundant list developed by combination of four separate sources." in: Molecular & cellular proteomics : MCP, Vol. 3, Issue 4, pp. 311-26, 2004 (PubMed).
Mori, Miura, Takeuchi, Igarashi, Sugiura, Saito, Oiso: "Gene amplification as a cause of inherited thyroxine-binding globulin excess in two Japanese families." in: The Journal of clinical endocrinology and metabolism, Vol. 80, Issue 12, pp. 3758-62, 1996 (PubMed).
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