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24. Polymorphisms in sulfotransferase 1A1 and glutathione S-transferase P1 genes in relation to colorectal cancer risk and patients' survival. Sun XF; Ahmadi A; Arbman G; Wallin A; Asklid D; Zhang H World J Gastroenterol; 2005 Nov; 11(43):6875-9. PubMed ID: 16425401 [TBL] [Abstract][Full Text] [Related]
26. The 3'-terminal exon of the family of steroid and phenol sulfotransferase genes is spliced at the N-terminal glycine of the universally conserved GXXGXXK motif that forms the sulfonate donor binding site. Chiba H; Komatsu K; Lee YC; Tomizuka T; Strott CA Proc Natl Acad Sci U S A; 1995 Aug; 92(18):8176-9. PubMed ID: 7667264 [TBL] [Abstract][Full Text] [Related]
27. Dissimilar neuropsychiatric presentations of two siblings with juvenile neuronal ceroid lipofuscinosis (Batten disease). Lee TS; Poon SH; Chang P J Neuropsychiatry Clin Neurosci; 2010; 22(1):123.E14-5. PubMed ID: 20160229 [No Abstract] [Full Text] [Related]
28. Three allele RFLP identified by an anonymous sequence on chromosome 2, E135 [D2S62]. Warnich L; Dietzsch E; Heyns DA; Vermaak LK; Herbert JS; Nicholson DL; Retief AE Nucleic Acids Res; 1989 Jan; 17(1):469. PubMed ID: 2563157 [No Abstract] [Full Text] [Related]
29. Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1. Travaglini L; Aiello C; Alesi V; Loddo S; Novelli A; Tozzi G; Bertini E; Leuzzi V; Brancati F Brain Dev; 2017 Feb; 39(2):182-183. PubMed ID: 27639779 [No Abstract] [Full Text] [Related]
30. Batten disease--an overview of research and funding. Rider JA Am J Med Genet; 1995 Jun; 57(2):128-9. PubMed ID: 7668315 [No Abstract] [Full Text] [Related]
31. Human phenol sulfotransferase STP2 gene: molecular cloning, structural characterization, and chromosomal localization. Her C; Raftogianis R; Weinshilboum RM Genomics; 1996 May; 33(3):409-20. PubMed ID: 8661000 [TBL] [Abstract][Full Text] [Related]
32. Reply to: Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1. Niida Y; Yokoi A; Kuroda M; Mitani Y; Nakagawa H; Ozaki M Brain Dev; 2017 Feb; 39(2):184-185. PubMed ID: 27616753 [No Abstract] [Full Text] [Related]
33. Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis). Taschner PE; de Vos N; Post JG; Meijers-Heijboer EJ; Hofman I; Loonen MC; Pinckers AJ; Bleeker-Wagemakers EM; Gardiner RM; Breuning MH Am J Med Genet; 1995 Jun; 57(2):333-7. PubMed ID: 7668358 [TBL] [Abstract][Full Text] [Related]
34. Human phenol sulfotransferase gene contains two alternative promoters: Structure and expression of the gene. Bernier F; Soucy P; Luu-The V DNA Cell Biol; 1996 May; 15(5):367-75. PubMed ID: 8924211 [TBL] [Abstract][Full Text] [Related]
35. Physical map of the region containing the gene for Batten disease (CLN3). Järvelä IE; Mitchison HM; Callen DF; Lerner TJ; Doggett NA; Taschner PE; Gardiner RM; Mole SE Am J Med Genet; 1995 Jun; 57(2):316-9. PubMed ID: 7668354 [TBL] [Abstract][Full Text] [Related]
36. Classification of the neuronal ceroid-lipofuscinoses: expansion of the atypical forms. Dyken P; Wisniewski K Am J Med Genet; 1995 Jun; 57(2):150-4. PubMed ID: 7668320 [TBL] [Abstract][Full Text] [Related]