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Single-Domain Parvulins Constitute a Specific Marker for Recently Proposed Deep-Branching Archaeal Subgroups.
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- Evolutionary Bioinformatics, 2011, n. 7, p. 135, doi. 10.4137/EBO.S7683
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- Publication type:
- Article
PAPSS2 deficiency causes androgen excess via impaired DHEA sulfation--in vitro and in vivo studies in a family harboring two novel PAPSS2 mutations.
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- 2015
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- Publication type:
- journal article
Dimerization of the Sodium/Iodide Symporter.
- Published in:
- Thyroid, 2019, v. 29, n. 10, p. 1485, doi. 10.1089/thy.2019.0034
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- Publication type:
- Article
A COMPARATIVE ANALYSIS OF IMPAIRED AND STANDARDIZED GAIT, FOCUSED ON LOWER EXTREMITIES, USING A MARKERLESS MOTION CAPTURE SYSTEM.
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- Biomedical Sciences Instrumentation, 2017, v. 53, p. 303
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- Publication type:
- Article
Human PAPS Synthase Isoforms Are Dynamically Regulated Enzymes with Access to Nucleus and Cytoplasm.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029559
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- Article
Adenosine-5′-phosphosulfate - a multifaceted modulator of bifunctional 3′-phospho-adenosine-5′-phosphosulfate synthases and related enzymes.
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- FEBS Journal, 2013, v. 280, n. 13, p. 3050, doi. 10.1111/febs.12252
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- Publication type:
- Article
The solution structure of pGolemi, a high affinity Mena EVH1 binding miniature protein, suggests explanations for paralog-specific binding to Ena/VASP homology (EVH) 1 domains.
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- Biological Chemistry, 2009, v. 390, n. 5/6, p. 417, doi. 10.1515/BC.2009.045
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- Publication type:
- Article
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series.
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- European Journal of Endocrinology, 2021, v. 185, n. 5, p. 729, doi. 10.1530/EJE-21-0152
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- Publication type:
- Article