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Cell cultures in uterine leiomyomas: Rapid disappearance of cells carrying MED12 mutations

Genes chromosomes & cancer, 2014-04, Vol.53 (4), p.317-323

2014

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MED12 mutations in uterine fibroids-their relationship to cytogenetic subgroups

International journal of cancer, 2012-10, Vol.131 (7), p.1528-1536

2012

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Fibroid explants reveal a higher sensitivity against MDM2-inhibitor nutlin-3 than matching myometrium

BMC women's health, 2012-01, Vol.12 (1), p.2-2, Article 2

2012

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Uterine fibroids: do we deal with more than one disease?

International journal of gynecological pathology, 2014-11, Vol.33 (6), p.568-572

2014

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Overexpression of HMGA2 in uterine leiomyomas points to its general role for the pathogenesis of the disease

Genes chromosomes & cancer, 2009-02, Vol.48 (2), p.171-178

2009

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A rare coincidence of different types of driver mutations among uterine leiomyomas (UL)

Molecular cytogenetics, 2015-10, Vol.8 (1), p.76, Article 76

2015

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HMGA2 expression in the PC-3 prostate cancer cell line is autonomous of growth factor stimulation

Anticancer research, 2013-08, Vol.33 (8), p.3069-3078

2013

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HMGA2 and p14Arf: major roles in cellular senescence of fibroids and therapeutic implications

Anticancer research, 2011-03, Vol.31 (3), p.753-761

2011

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HMGI-C rearrangements as the molecular basis for the majority of pulmonary chondroid hamartomas: a survey of 30 tumors

Oncogene, 1996-02, Vol.12 (3), p.515-521

1996

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A high frequency of tumors with rearrangements of genes of the HMGI(Y) family in a series of 191 pulmonary chondroid hamartomas

Genes chromosomes & cancer, 1999-10, Vol.26 (2), p.125-133

1999

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Description of a novel fusion transcript between HMGI-C, a gene encoding for a member of the high mobility group proteins, and the mitochondrial aldehyde dehydrogenase gene

Cancer research (Chicago, Ill.), 1995-12, Vol.55 (24), p.6038-6039

1995

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Chromosomal translocations affecting 12q14–15 but not deletions of the long arm of chromosome 7 associated with a growth advantage of uterine smooth muscle cells

Molecular human reproduction, 1999-12, Vol.5 (12), p.1150-1154

1999

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Re: Sit, DNA, Sit: Cancer Genetics Going to the Dogs

JNCI : Journal of the National Cancer Institute, 1999-10, Vol.91 (19), p.1688-1689

1999

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Ten Pulmonary Chondroid Hamartomas With Chromosome 6p21 Breakpoints Within the HMG-I(Y) Gene or Its Immediate Surroundings

JNCI : Journal of the National Cancer Institute, 1996-09, Vol.88 (17), p.1234-1236

1996

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Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors

The American journal of pathology, 1998-02, Vol.152 (2), p.431-435

1998

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Cytogenetic and molecular analysis of an aggressive angiomyxoma

The American journal of pathology, 1995-09, Vol.147 (3), p.580-585

1995

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Rearrangements of the high mobility group protein family genes and the molecular genetic origin of uterine leiomyomas and endometrial polyps

Molecular human reproduction, 1996-04, Vol.2 (4), p.277-283

1996

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A new banding pattern of human chromosomes by in situ nick translation using ECO RI and biotin-dUTP

Clinical genetics, 1985-08, Vol.28 (2), p.173-176

1985

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A characteristic sequence of trisomies starting with trisomy 7 in benign thyroid tumors

Human genetics, 1994-08, Vol.94 (2), p.198-202

1994

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Follicular thyroid carcinoma: Chromosome analysis of 19 cases

Genes chromosomes & cancer, 1998-03, Vol.21 (3), p.250-255

1998

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A fibroadenoma with a t(4;12) (q27;q15) affecting the HMGI-C gene, a member of the high mobility group protein gene family

Breast cancer research and treatment, 1996-01, Vol.38 (3), p.299-303

1996

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Physical Mapping of Chromosome 12q Breakpoints in Lipoma, Pleomorphic Salivary Gland Adenoma, Uterine Leiomyoma, and Myxoid Liposarcoma

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.210-222

1994

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Selective Loss of Integrated Epstein-Barr Virus Genomes after Long-Term Cultivation of Burkitt's Lymphoma × B-Lymphoblastoid Cell Hybrids Due to Chromatin Instability at the Integration Site

Virology (New York, N.Y.), 1995-09, Vol.212 (1), p.179-185

1995

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Trisomy 8 as a recurrent clonal abnormality in breast cancer?

Cancer genetics and cytogenetics, 1993, Vol.65 (1), p.64-67

1993

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Molecular characterization of mar, a multiple aberration region on human chromosome segment 12q13-q15 implicated in various solid tumors

Genes chromosomes & cancer, 1995-04, Vol.12 (4), p.296-303

1995

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Cell cultures in uterine leiomyomas: Rapid disappearance of cells carrying MED12 mutations

MED12 mutations in uterine fibroids-their relationship to cytogenetic subgroups

Fibroid explants reveal a higher sensitivity against MDM2-inhibitor nutlin-3 than matching myometrium

Uterine fibroids: do we deal with more than one disease?

Overexpression of HMGA2 in uterine leiomyomas points to its general role for the pathogenesis of the disease

A rare coincidence of different types of driver mutations among uterine leiomyomas (UL)

HMGA2 expression in the PC-3 prostate cancer cell line is autonomous of growth factor stimulation

HMGA2 and p14Arf: major roles in cellular senescence of fibroids and therapeutic implications

HMGI-C rearrangements as the molecular basis for the majority of pulmonary chondroid hamartomas: a survey of 30 tumors

A high frequency of tumors with rearrangements of genes of the HMGI(Y) family in a series of 191 pulmonary chondroid hamartomas

Description of a novel fusion transcript between HMGI-C, a gene encoding for a member of the high mobility group proteins, and the mitochondrial aldehyde dehydrogenase gene

Chromosomal translocations affecting 12q14–15 but not deletions of the long arm of chromosome 7 associated with a growth advantage of uterine smooth muscle cells

Re: Sit, DNA, Sit: Cancer Genetics Going to the Dogs

Ten Pulmonary Chondroid Hamartomas With Chromosome 6p21 Breakpoints Within the HMG-I(Y) Gene or Its Immediate Surroundings

Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors

Cytogenetic and molecular analysis of an aggressive angiomyxoma

Rearrangements of the high mobility group protein family genes and the molecular genetic origin of uterine leiomyomas and endometrial polyps

A new banding pattern of human chromosomes by in situ nick translation using ECO RI and biotin-dUTP

A characteristic sequence of trisomies starting with trisomy 7 in benign thyroid tumors

Follicular thyroid carcinoma: Chromosome analysis of 19 cases

A fibroadenoma with a t(4;12) (q27;q15) affecting the HMGI-C gene, a member of the high mobility group protein gene family

Physical Mapping of Chromosome 12q Breakpoints in Lipoma, Pleomorphic Salivary Gland Adenoma, Uterine Leiomyoma, and Myxoid Liposarcoma

Selective Loss of Integrated Epstein-Barr Virus Genomes after Long-Term Cultivation of Burkitt's Lymphoma × B-Lymphoblastoid Cell Hybrids Due to Chromatin Instability at the Integration Site

Trisomy 8 as a recurrent clonal abnormality in breast cancer?

Molecular characterization of mar, a multiple aberration region on human chromosome segment 12q13-q15 implicated in various solid tumors

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