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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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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

Nature genetics, 1998-04, Vol.18 (4), p.319-324

1998

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Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene

Human genetics, 2001-06, Vol.108 (6), p.546-551

2001

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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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Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer

Oncogene, 2017-08, Vol.36 (31), p.4469-4480

2017

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CARD15/NOD2 Risk Alleles in the Development of Crohn's Disease in the Australian Population

Annals of human genetics, 2003-01, Vol.67 (1), p.35-41

2003

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Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

Nature genetics, 1996-11, Vol.14 (3), p.320-323

1996

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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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Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis

Journal of clinical pathology, 2008-01, Vol.61 (1), p.59-63

2008

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A familial cryptic subtelomeric deletion 12p with variable phenotypic effect

Clinical genetics, 2002-03, Vol.61 (3), p.198-201

2002

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Integration of cytogenetic landmarks into the draft sequence of the human genome

Nature (London), 2001-02, Vol.409 (6822), p.953-958

2001

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Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16

Annals of human genetics, 1998-07, Vol.62 (4), p.291-298

1998

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Localization of Human Cadherin Genes to Chromosome Regions Exhibiting Cancer-Related Loss of Heterozygosity

Genomics (San Diego, Calif.), 1998-05, Vol.49 (3), p.467-471

1998

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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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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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A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction

Chromosoma, 2002-09, Vol.111 (3), p.170-175

2002

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The Batten Disease Gene Product (CLN3p) Is a Golgi Integral Membrane Protein

Human molecular genetics, 1999-03, Vol.8 (3), p.523-531

1999

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Molecular cloning and physical and genetic mapping of a novel human Na +/H + exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Genomics (San Diego, Calif.), 1995-02, Vol.25 (3), p.615-622

1995

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Genetic association of 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks

Hypertension (Dallas, Tex. 1979), 1996-09, Vol.28 (3), p.478-482

1996

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Chromosomal origin of small ring marker chromosomes in man : characterization by molecular genetics

American journal of human genetics, 1991-04, Vol.48 (4), p.769-782

1991

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Localization of the human multiple drug resistance gene, MDR1, to 7q21.1

Human genetics, 1987-10, Vol.77 (2), p.142-144

1987

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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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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

Volltextzugriff (PDF)

Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

Genomics (San Diego, Calif.), 1998-09, Vol.52 (3), p.325-331

1998

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Assignment of the Human CC Chemokine Gene TARC (SCYA17) to Chromosome 16q13

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.211-213

1997

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

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene

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

Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer

CARD15/NOD2 Risk Alleles in the Development of Crohn's Disease in the Australian Population

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

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

Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect

Integration of cytogenetic landmarks into the draft sequence of the human genome

Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16

Localization of Human Cadherin Genes to Chromosome Regions Exhibiting Cancer-Related Loss of Heterozygosity

Systematic characterisation of the rat and human CYP24A1 promoter

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

A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction

The Batten Disease Gene Product (CLN3p) Is a Golgi Integral Membrane Protein

Molecular cloning and physical and genetic mapping of a novel human Na +/H + exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Genetic association of 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks

Chromosomal origin of small ring marker chromosomes in man : characterization by molecular genetics

Localization of the human multiple drug resistance gene, MDR1, to 7q21.1

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

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

Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

Assignment of the Human CC Chemokine Gene TARC (SCYA17) to Chromosome 16q13

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