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MEN2A-RET-induced cellular transformation by activation of STAT3

Oncogene, 2001-08, Vol.20 (38), p.5350-5358

2001

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In Vitro Fertilization with Preimplantation Genetic Screening

The New England journal of medicine, 2007-07, Vol.357 (1), p.9-17

2007

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A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3

European journal of human genetics : EJHG, 1999-05, Vol.7 (4), p.478-486

1999

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Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

Journal of the American College of Cardiology, 2007-06, Vol.49 (25), p.2430-2439

2007

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RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor

Cancer research (Chicago, Ill.), 2005-03, Vol.65 (5), p.1729-1737

2005

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A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

Nature (London), 1994-01, Vol.367 (6461), p.375-376

1994

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Telomeres, Telomerase, and Cancer

The New England journal of medicine, 2000-04, Vol.342 (17), p.1282-1283

Buys, Charles H.C.M

2000

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Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Genes chromosomes & cancer, 2006-07, Vol.45 (7), p.676-691

2006

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Localizing a putative mutation as the major contributor to the development of sporadic hirschsprung disease to the RET genomic sequence between the promoter region and exon 2

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.604-612

2004

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An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures

Prenatal diagnosis, 2006-09, Vol.26 (9), p.855-860

2006

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Ras/ERK1/2-mediated STAT3 Ser super(727) Phosphorylation by Familial Medullary Thyroid Carcinoma-associated RET Mutants Induces Full Activation of STAT3 and Is Required for c-fos Promoter Activation, Cell Mitogenicity, and Transformation

The Journal of biological chemistry, 2007-03, Vol.282 (9), p.6415-6424

2007

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Homozygous arginine-72 in wild type p53 and risk of cervical cancer

The Lancet (British edition), 1998-11, Vol.352 (9142), p.1756-1756

1998

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A substantial proportion of microsatellite-unstable colon tumors carry TP53 mutations while not showing chromosomal instability

Genes chromosomes & cancer, 2005-06, Vol.43 (2), p.194-201

2005

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SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion

European journal of human genetics : EJHG, 2000-02, Vol.8 (2), p.79-86

2000

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High Frequency of TP53 Mutations in Juvenile Pilocytic Astrocytomas Indicates Role of TP53 in the Development of These Tumors

Brain pathology (Zurich, Switzerland), 1999-07, Vol.9 (3), p.463-467

1999

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SMA carrier testing - validation of hemizygous SMN exon7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion

European journal of human genetics : EJHG, 2000-02, Vol.8 (2), p.79-86

2000

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Molecular analysis of renal cell carcinoma

Cancer genetics and cytogenetics, 1991-04, Vol.52 (2), p.244-244

1991

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P53 mutations in human lung tumors

Cancer research (Baltimore), 1992-04, Vol.52 (7), p.1695-1698

1992

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MEN2A-RET-induced cellular transformation by activation of STAT3

In Vitro Fertilization with Preimplantation Genetic Screening

A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3

Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

Telomeres, Telomerase, and Cancer

Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Localizing a putative mutation as the major contributor to the development of sporadic hirschsprung disease to the RET genomic sequence between the promoter region and exon 2

An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures

Ras/ERK1/2-mediated STAT3 Ser super(727) Phosphorylation by Familial Medullary Thyroid Carcinoma-associated RET Mutants Induces Full Activation of STAT3 and Is Required for c-fos Promoter Activation, Cell Mitogenicity, and Transformation

Homozygous arginine-72 in wild type p53 and risk of cervical cancer

A substantial proportion of microsatellite-unstable colon tumors carry TP53 mutations while not showing chromosomal instability

SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion

High Frequency of TP53 Mutations in Juvenile Pilocytic Astrocytomas Indicates Role of TP53 in the Development of These Tumors

SMA carrier testing - validation of hemizygous SMN exon7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion

Molecular analysis of renal cell carcinoma

P53 mutations in human lung tumors

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