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A Mouse Model Demonstrates a Multigenic Origin of Congenital Hypothyroidism

Endocrinology (Philadelphia), 2005-12, Vol.146 (12), p.5038-5047

2005

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Novel anti-obesity quercetin-derived Q2 prevents metabolic disorders in rats fed with high-fat diet

Vascular pharmacology, 2018-04, Vol.103-105, p.58-58

2018

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Missense Mutation in the Transcription Factor NKX2–5: A Novel Molecular Event in the Pathogenesis of Thyroid Dysgenesis

The journal of clinical endocrinology and metabolism, 2006-04, Vol.91 (4), p.1428-1433

2006

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Increased Sensitivity to Thyroid Hormone in Mice with Complete Deficiency of Thyroid Hormone Receptor α

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (1), p.349-354

2001

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A mouse model for hereditary thyroid dysgenesis and cleft palate

Nature genetics, 1998-08, Vol.19 (4), p.395-398

1998

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PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

Nature genetics, 1998-05, Vol.19 (1), p.83-86

1998

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Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes

Journal of endocrinology, 2002-01, Vol.172 (1), p.177-185

2002

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Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LH

Development (Cambridge), 1998-04, Vol.125 (7), p.1229-1239

1998

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High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy

Journal of endocrinological investigation, 2001-03, Vol.24 (3), p.152-158

2001

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Autosomal Dominant Resistance to Thyrotropin as a Distinct Entity in Five Multigenerational Kindreds: Clinical Characterization and Exclusion of Candidate Loci

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4025-4034

2005

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Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)

Biochimie, 1999-05, Vol.81 (5), p.433-440

1999

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Molecular genetics of congenital hypothyroidism

Current opinion in genetics & development, 1999-06, Vol.9 (3), p.289-294

1999

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RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor

American journal of physiology: endocrinology and metabolism, 2002-08, Vol.283 (2), p.E326-E331

2002

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Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-Phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathy

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.3790-3794

1998

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Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis

Thyroid (New York, N.Y.), 1997-06, Vol.7 (3), p.383-387

1997

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Structural defects of a Pax8 mutant that give rise to congenital hypothyroidism

Biochemical journal, 1999-07, Vol.341 ( Pt 1) (1), p.89-93

1999

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Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I

The journal of clinical endocrinology and metabolism, 1995-12, Vol.80 (12), p.3744-3749

1995

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Integrin expression in thyroid cells from normal glands and nodular goiters

The journal of clinical endocrinology and metabolism, 1993-06, Vol.76 (6), p.1575-1579

1993

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Epidermal growth factor receptor in human brain tumors

Journal of endocrinological investigation, 1992, Vol.15 (1), p.31-37

1992

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Recent advances in understanding the molecular basis of primary congenital hypothyroidism

Molecular Medicine Today, 2000, Vol.6 (1), p.36-42

Macchia, Paolo E

2000

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Epidermal growth factor receptor and lipid membrane components in human lung cancers

Journal of endocrinological investigation, 1993-02, Vol.16 (2), p.99-107

1993

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Gangliosides and phospholipids in human thyroids responsive and unresponsive to thyrotropin

Journal of endocrinological investigation, 1990-11, Vol.13 (10), p.817-823

1990

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Expression of thyroid transcription factor 1 gene can be regulated at the transcriptional and posttranscriptional levels

Cell growth & differentiation, 1996-02, Vol.7 (2), p.251-261

1996

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Immune recognition of porin and lipopolysaccharide epitopes of Salmonella typhimurium in mice

Microbial pathogenesis, 2000-03, Vol.28 (3), p.157-167

2000

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Recognition specificity of monoclonal antibodies which protect mice against Salmonella typhimurium infection

Research in microbiology, 1999-07, Vol.150 (6), p.385-394

1999

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Transcription Factors - Genetics
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A Mouse Model Demonstrates a Multigenic Origin of Congenital Hypothyroidism

Novel anti-obesity quercetin-derived Q2 prevents metabolic disorders in rats fed with high-fat diet

Missense Mutation in the Transcription Factor NKX2–5: A Novel Molecular Event in the Pathogenesis of Thyroid Dysgenesis

Increased Sensitivity to Thyroid Hormone in Mice with Complete Deficiency of Thyroid Hormone Receptor α

A mouse model for hereditary thyroid dysgenesis and cleft palate

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes

Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LH

High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy

Autosomal Dominant Resistance to Thyrotropin as a Distinct Entity in Five Multigenerational Kindreds: Clinical Characterization and Exclusion of Candidate Loci

Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)

Molecular genetics of congenital hypothyroidism

RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor

Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-Phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathy

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis

Structural defects of a Pax8 mutant that give rise to congenital hypothyroidism

Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I

Integrin expression in thyroid cells from normal glands and nodular goiters

Epidermal growth factor receptor in human brain tumors

Recent advances in understanding the molecular basis of primary congenital hypothyroidism

Epidermal growth factor receptor and lipid membrane components in human lung cancers

Gangliosides and phospholipids in human thyroids responsive and unresponsive to thyrotropin

Expression of thyroid transcription factor 1 gene can be regulated at the transcriptional and posttranscriptional levels

Immune recognition of porin and lipopolysaccharide epitopes of Salmonella typhimurium in mice

Recognition specificity of monoclonal antibodies which protect mice against Salmonella typhimurium infection

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