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Splice variants but not mutations of DNA polymerase β are common in bladder cancer

Cancer research (Chicago, Ill.), 2002-06, Vol.62 (11), p.3251-3256

2002

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Microsatellite–Centromere Mapping in the Zebrafish (Danio rerio)

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.337-341

1995

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Daytime sleepiness and REM abnormalities in Prader-Willi syndrome : Evidence of generalized hypoarousal

International journal of neuroscience, 1996-11, Vol.87 (3-4), p.127-139

1996

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Bloom syndrome and maternal uniparental disomy for chromosome 15

American journal of human genetics, 1994-07, Vol.55 (1), p.74-80

1994

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Tandem machine learning for the identification of genes regulated by transcription factors

BMC bioinformatics, 2005-08, Vol.6 (1), p.204-204, Article 204

2005

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Sequence-Based, in situ detection of chromosomal abnormalities at high resolution

American journal of medical genetics, 2003-09, Vol.121A (3), p.245-257

2003

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Phylogenetic inference based on information theory-based PCR amplification

Journal of phytopathology, 1998-09, Vol.146 (8/9), p.427-430

1998

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A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region

Human molecular genetics, 1994-10, Vol.3 (10), p.1912-1912

1994

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Organization of the ABCR gene: analysis of promoter and splice junction sequences

Gene, 1998-07, Vol.215 (1), p.111-122

1998

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Intensity Integrated Laplacian-Based Thickness Measurement for Detecting Human Metaphase Chromosome Centromere Location

IEEE transactions on biomedical engineering, 2013-07, Vol.60 (7), p.2005-2013

2013

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Racial Differences in Allelic Distribution at the Human Pulmonary Surfactant Protein B Gene Locus (SP-B)

Experimental lung research, 1996, Vol.22 (4), p.489-494

1996

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Automated splicing mutation analysis by information theory

Human mutation, 2005-04, Vol.25 (4), p.334-342

2005

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Automating dicentric chromosome detection from cytogenetic biodosimetry data

Radiation protection dosimetry, 2014-06, Vol.159 (1-4), p.95-104

2014

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Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression

The Journal of pharmacology and experimental therapeutics, 2003-12, Vol.307 (3), p.906-922

2003

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Interpretation, Stratification and Evidence for Sequence Variants Affecting mRNA Splicing in Complete Human Genome Sequences

Genomics, proteomics & bioinformatics, 2013-04, Vol.11 (2), p.77-85

2013

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Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes

American journal of respiratory cell and molecular biology, 1996-10, Vol.15 (4), p.489-498

1996

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Development of a directory of genetic probes as a shared institutional resource

Computer methods and programs in biomedicine, 1995, Vol.46 (1), p.35-39

1995

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L1 repeat elements in the human ε-Gγ-globin gene intergenic region: sequence analysis and concerted evolution within this family

Molecular biology and evolution, 1987-07, Vol.4 (4), p.327-342

1987

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Using information content and base frequencies to distinguish mutations from genetic polymorphisms in splice junction recognition sites

Human mutation, 1995, Vol.6 (1), p.74-76

1995

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Hydration in purple membrane as a function of relative humidity

Journal of molecular biology, 1981-01, Vol.145 (1), p.281-284

1981

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Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A>G; IVS11-2A>G; L78833, 37698, A>G

Human mutation, 2000-09, Vol.16 (3), p.264-264

2000

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Conservation in the 5' region of the long interspersed mouse L1 repeat: implications of comparative sequence analysis

Nucleic acids research, 1986-04, Vol.14 (7), p.3119-3136

1986

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Automatic detection of noisy spots in two-dimensional Southern blots. International Electrophoresis Society Meeting, Washington DC, March 16-19, 1991

Applied and theoretical electrophoresis, 1991, Vol.2 (4-5), p.141

1991

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Loss of heterozygosity and microsatellite instability at the retinoblastoma locus in osteosarcomas

Diagnostic molecular pathology, 1996-09, Vol.5 (3), p.214-219

1996

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BIPAD: a web server for modeling bipartite sequence elements

BMC bioinformatics, 2006-02, Vol.7 (1), p.76-76, Article 76

2006

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Splice variants but not mutations of DNA polymerase β are common in bladder cancer

Microsatellite–Centromere Mapping in the Zebrafish (Danio rerio)

Daytime sleepiness and REM abnormalities in Prader-Willi syndrome : Evidence of generalized hypoarousal

Bloom syndrome and maternal uniparental disomy for chromosome 15

Tandem machine learning for the identification of genes regulated by transcription factors

Sequence-Based, in situ detection of chromosomal abnormalities at high resolution

Phylogenetic inference based on information theory-based PCR amplification

A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region

Organization of the ABCR gene: analysis of promoter and splice junction sequences

Intensity Integrated Laplacian-Based Thickness Measurement for Detecting Human Metaphase Chromosome Centromere Location

Racial Differences in Allelic Distribution at the Human Pulmonary Surfactant Protein B Gene Locus (SP-B)

Automated splicing mutation analysis by information theory

Automating dicentric chromosome detection from cytogenetic biodosimetry data

Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression

Interpretation, Stratification and Evidence for Sequence Variants Affecting mRNA Splicing in Complete Human Genome Sequences

Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes

Development of a directory of genetic probes as a shared institutional resource

L1 repeat elements in the human ε-Gγ-globin gene intergenic region: sequence analysis and concerted evolution within this family

Using information content and base frequencies to distinguish mutations from genetic polymorphisms in splice junction recognition sites

Hydration in purple membrane as a function of relative humidity

Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A>G; IVS11-2A>G; L78833, 37698, A>G

Conservation in the 5' region of the long interspersed mouse L1 repeat: implications of comparative sequence analysis

Automatic detection of noisy spots in two-dimensional Southern blots. International Electrophoresis Society Meeting, Washington DC, March 16-19, 1991

Loss of heterozygosity and microsatellite instability at the retinoblastoma locus in osteosarcomas

BIPAD: a web server for modeling bipartite sequence elements

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