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Mutant p53 drives invasion in breast tumors through up-regulation of miR-155

Oncogene, 2013-06, Vol.32 (24), p.2992-3000

2013

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Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11

Oncogene, 2012-06, Vol.31 (23), p.2836-2848

2012

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Systematic characterisation of the rat and human CYP24A1 promoter

Molecular and cellular endocrinology, 2010-08, Vol.325 (1), p.46-53

2010

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Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease

Biochemical and biophysical research communications, 1994-11, Vol.205 (1), p.482-489

1994

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Incidence and origin of null alleles in the (AC)n microsatellite markers

American journal of human genetics, 1993-05, Vol.52 (5), p.922-927

1993

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Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13 1

Cytogenetic and genome research, 1998, Vol.81 (1), p.10-11

1998

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Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis

Science (American Association for the Advancement of Science), 1994-06, Vol.264 (5167), p.1938-1941

1994

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Mapping the short arm of human chromosome 16

Genomics (San Diego, Calif.), 1989-04, Vol.4 (3), p.348-354

1989

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Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications

The Lancet (British edition), 1994-06, Vol.343 (8912), p.1531-1534

1994

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Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

Hormone research, 2004-01, Vol.62 (4), p.208-214

2004

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Isolation and characterisation of (AC) n microsatellite genetic markers from human chromosome 16

Genomics (San Diego, Calif.), 1992-06, Vol.13 (2), p.402-408

1992

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Genomic structure and expression analysis of the spastic paraplegia gene, SPG7

Human genetics, 1999-07, Vol.105 (1-2), p.139-144

1999

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ARA,a Novel ABC Transporter, Is Located at 16p13.1, Is Deleted in inv(16) Leukemias, and Is Shown To Be Expressed in Primitive Hematopoietic Precursors

Genomics (San Diego, Calif.), 1998-08, Vol.51 (3), p.455-458

1998

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Integration of Transcript and Genetic Maps of Chromosome 16 at Near-1-Mb Resolution: Demonstration of a “Hot Spot” for Recombination at 16p12

Genomics (San Diego, Calif.), 1995-09, Vol.29 (2), p.503-511

1995

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Structure and chromosomal localization of the human renal kallikrein gene

Biochemistry (Easton), 1988-05, Vol.27 (9), p.3124-3129

1988

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Genomic structure and expression analysis of the spastic paraplegia gene, SPG7

Human genetics, 1999-08, Vol.105 (1-2), p.139-144

1999

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High-resolution cytogenetic-based physical map of human chromosome 16

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1178-1185

1992

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The gene for the human IgA Fc receptor maps to 19q13.4

Human genetics, 1992-04, Vol.89 (1), p.107-108

1992

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Chromosomal assignment of the human deoxyribonuclease I gene, DNASE1 (DNL1), to band 16p13.3 using the polymerase chain reaction

Cytogenetic and genome research, 1995-01, Vol.70 (3-4), p.221-223

1995

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Toxic and genetic effects of fuel oil photoproducts and three hydroperoxides in Saccharomyces cerevisiae [Yeasts]

Journal of toxicology and environmental health, 1978-09, Vol.4 (5/6), p.913-917

1978

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Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.455-460

1993

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Localization of the gene for human 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) to chromosome band 16q22

Cytogenetic and genome research, 1995-01, Vol.71 (2), p.124-125

1995

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A PCR-Based Genetic Linkage Map of Human Chromosome 16

Genomics (San Diego, Calif.), 1994-07, Vol.22 (1), p.68-76

1994

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Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.169-175

1994

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A New DNA Marker Tightly Linked to the Fragile X Locus (FRAXA)

Science (American Association for the Advancement of Science), 1989-12, Vol.246 (4935), p.1298-1300

1989

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Mutant p53 drives invasion in breast tumors through up-regulation of miR-155

Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11

Systematic characterisation of the rat and human CYP24A1 promoter

Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease

Incidence and origin of null alleles in the (AC)n microsatellite markers

Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13 1

Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis

Mapping the short arm of human chromosome 16

Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications

Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

Isolation and characterisation of (AC) n microsatellite genetic markers from human chromosome 16

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7

ARA,a Novel ABC Transporter, Is Located at 16p13.1, Is Deleted in inv(16) Leukemias, and Is Shown To Be Expressed in Primitive Hematopoietic Precursors

Integration of Transcript and Genetic Maps of Chromosome 16 at Near-1-Mb Resolution: Demonstration of a “Hot Spot” for Recombination at 16p12

Structure and chromosomal localization of the human renal kallikrein gene

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7

High-resolution cytogenetic-based physical map of human chromosome 16

The gene for the human IgA Fc receptor maps to 19q13.4

Chromosomal assignment of the human deoxyribonuclease I gene, DNASE1 (DNL1), to band 16p13.3 using the polymerase chain reaction

Toxic and genetic effects of fuel oil photoproducts and three hydroperoxides in Saccharomyces cerevisiae [Yeasts]

Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

Localization of the gene for human 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) to chromosome band 16q22

A PCR-Based Genetic Linkage Map of Human Chromosome 16

Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

A New DNA Marker Tightly Linked to the Fragile X Locus (FRAXA)

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