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Tiina Robins

Research Profile

Chemicals & Drugs

Disorders

Anatomy

COS Cells

Genes & Molecular Sequences

Amino Acid Sequences

Physiology

Concepts & Ideas

Procedures

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Publications

TOP 3
Tiina Robins; Christine Bellanne-Chantelot; Michela Barbaro; Sylvie Cabrol; Anna Wedell; Svetlana Lajic
Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.
Tiina Robins; Jonas Carlsson; Maria Sunnerhagen; Anna Wedell; Bengt Persson
Molecular model of human CYP21 based on mammalian CYP2C5: structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia.
Michela Barbaro; Lilia Baldazzi; Antonio Balsamo; Svetlana Lajic; Tiina Robins; L Barp; Piero Pirazzoli; Emanuele Cacciari; Alessandro Cicognani; Anna Wedell
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene.

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All Publications

2007: Tiina Robins; Christine Bellanne-Chantelot; Michela Barbaro; Sylvie Cabrol; Anna Wedell; Svetlana Lajic
Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.
Journal of molecular medicine (Berlin, Germany) 2007;85(3):247-55.
2006: Tiina Robins; Jonas Carlsson; Maria Sunnerhagen; Anna Wedell; Bengt Persson
Molecular model of human CYP21 based on mammalian CYP2C5: structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia.
Molecular endocrinology (Baltimore, Md.) 2006;20(11):2946-64.
2006: Michela Barbaro; Lilia Baldazzi; Antonio Balsamo; Svetlana Lajic; Tiina Robins; L Barp; Piero Pirazzoli; Emanuele Cacciari; Alessandro Cicognani; Anna Wedell
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene.
Journal of molecular medicine (Berlin, Germany) 2006;84(6):521-8.
2005: Tiina Robins; Michela Barbaro; Svetlana Lajic; Anna Wedell
Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia.
The Journal of clinical endocrinology and metabolism 2005;90(4):2148-53.
2002: Svetlana Lajić; Séverine Clauin; Tiina Robins; Patrick Vexiau; Hélène Blanché; Christine Bellanne-Chantelot; Anna Wedell
Novel mutations in CYP21 detected in individuals with hyperandrogenism.
The Journal of clinical endocrinology and metabolism 2002;87(6):2824-9.
2001: S Lajić; Tiina Robins; N Krone; H P Schwarz; Anna Wedell
CYP21 mutations in simple virilizing congenital adrenal hyperplasia.
Journal of molecular medicine (Berlin, Germany) 2001;79(10):581-6.

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