Found: 15
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Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1159, doi. 10.3390/ijms23031159
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- Publication type:
- Article
Molecular Diagnosis of Analbuminemia: A New Case Caused by a Nonsense Mutation in the Albumin Gene.
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- International Journal of Molecular Sciences, 2011, v. 12, n. 11, p. 7314, doi. 10.3390/ijms12117314
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- Publication type:
- Article
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene.
- Published in:
- Annals of Laboratory Medicine, 2018, v. 38, n. 2, p. 185, doi. 10.3343/alm.2018.38.2.185
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- Publication type:
- Article
A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 12, p. 2221, doi. 10.1515/cclm-2012-0390
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- Publication type:
- Article
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 10, p. 1311, doi. 10.1515/CCLM.2009.289
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- Publication type:
- Article
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia.
- Published in:
- Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/8452564
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- Publication type:
- Article
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family.
- Published in:
- Biochemia Medica, 2016, v. 26, n. 2, p. 264, doi. 10.11613/BM.2016.031
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- Publication type:
- Article
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene.
- Published in:
- Biochemia Medica, 2014, v. 24, n. 1, p. 151, doi. 10.11613/BM.2014.017
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- Publication type:
- Article
Kvaliteta slika elektroforeze i izoelektričnog fokusiranja komprimiranih primjenom JPEG i JPEG2000.
- Published in:
- Biochemia Medica, 2007, v. 17, n. 2, p. 220
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- Publication type:
- Article
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00336
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- Article
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant.
- Published in:
- 2016
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- Publication type:
- journal article
Identification of the amniotic fluid insulin-like growth factor binding protein-1 phosphorylation sites and propensity to proteolysis of the isoforms.
- Published in:
- FEBS Journal, 2009, v. 276, n. 20, p. 6033, doi. 10.1111/j.1742-4658.2009.07318.x
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- Publication type:
- Article
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia.
- Published in:
- European Journal of Clinical Investigation, 2013, v. 43, n. 1, p. 72, doi. 10.1111/eci.12019
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- Publication type:
- Article
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin.
- Published in:
- 2008
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- Publication type:
- Other
Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia.
- Published in:
- Frontiers in Endocrinology, 2017, p. 1, doi. 10.3389/fendo.2017.00297
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- Publication type:
- Article