Literature DB >> 1870994

Trinucleotide repeat polymorphism at the human transcription factor IID gene.

M H Polymeropoulos1, D S Rath, H Xiao, C R Merril.   

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Year:  1991        PMID： 1870994      PMCID： PMC328594          DOI： 10.1093/nar/19.15.4307

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Cloning of a transcriptionally active human TATA binding factor.

Authors:  C C Kao; P M Lieberman; M C Schmidt; Q Zhou; R Pei; A J Berk
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2.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025
  2 in total
  7 in total

1.  Variation in short tandem repeat sequences--a survey of twelve microsatellite loci for use as forensic identification markers.

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2.  Loss of heterozygosity at chromosome 6q in preinvasive and early invasive breast carcinomas.

Authors:  S A Chappell; T Walsh; R A Walker; J A Shaw
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

3.  Exclusion of familial dysautonomia from more than 60% of the genome.

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Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

Review 4.  Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.

Authors:  Christine Zühlke; Katrin Bürk
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5.  Microsatellite instability in adenocarcinomas of the upper gastrointestinal tract. Relation to clinicopathological data and family history.

Authors:  G Keller; M Rotter; H Vogelsang; P Bischoff; K F Becker; J Mueller; H Brauch; J R Siewert; H Höfler
Journal:  Am J Pathol       Date:  1995-09       Impact factor: 4.307

6.  "Cryptic" repeating triplets of purines and pyrimidines (cRRY(i)) are frequent and polymorphic: analysis of coding cRRY(i) in the proopiomelanocortin (POMC) and TATA-binding protein (TBP) genes.

Authors:  B Gostout; Q Liu; S S Sommer
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

7.  Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes.

Authors:  Christine Zühlke; Andreas Dalski; Eberhard Schwinger; Ulrich Finckh
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