1,721,033 research outputs found
Structure of the SLC7A7 gene and mutational anolysis of patients affected by lysinuric protein intolerance.
No full textStructure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
No full textSLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family.
No full textStructure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
No full textSLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family.
No full textStructure of the SLC7A7 gene and mutational anolysis of patients affected by lysinuric protein intolerance.
No full text
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome
No full textThe blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report
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