1993
DOI: 10.1006/geno.1993.1494
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Mapping of the Phenol Sulfotransferase Gene (STP) to Human Chromosome 16p12.1-p11.2 and to Mouse Chromosome 7

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Cited by 60 publications
(14 citation statements)
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“…More recently, genetic linkage of the SULT1A locus and a predisposition to autism spectrum disorders (ASD) has been reported (Dooley et al, 1993;Kumar et al, 2008;Weiss et al, 2008). Furthermore, individuals with ASD have decreased expression of SULT1A isoforms in platelets and in the gastrointestinal tract (Waring et al, 1996;Waring and Klovrza, 2000;Whiteley and Shattock, 2002;Kern et al, 2004).…”
mentioning
confidence: 99%
“…More recently, genetic linkage of the SULT1A locus and a predisposition to autism spectrum disorders (ASD) has been reported (Dooley et al, 1993;Kumar et al, 2008;Weiss et al, 2008). Furthermore, individuals with ASD have decreased expression of SULT1A isoforms in platelets and in the gastrointestinal tract (Waring et al, 1996;Waring and Klovrza, 2000;Whiteley and Shattock, 2002;Kern et al, 2004).…”
mentioning
confidence: 99%
“…Recently, human phenol ST genes, SULT1A1 (alias STP1), SULT1A2 (alias STP2) and SULT1A3 (alias STM) were assigned to the same region on chromosome 16p12.1→ p11.2 , whereas the mouse phenol ST gene, Stp1 was mapped to mouse chromosome 7 (Dooley et al, 1993). These phenol ST genes appear to be orthologous in the three species .…”
Section: Resultsmentioning
confidence: 99%
“…and the thermolabile, or monoamine-pre ferring ("M") form (gene symbols STP and STM. respectively) have been mapped to human chromosome 16 (Dooley et al, 1993;Aksoy et al. 1994a).…”
Section: Resultsmentioning
confidence: 99%