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Up to date with human thyroglobulin

Journal of endocrinology, 2001-08, Vol.170 (2), p.307-321

2001

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Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene

Hormone and metabolic research, 2014-02, Vol.46 (2), p.100-108

2014

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New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

The journal of clinical endocrinology and metabolism, 2010-07, Vol.95 (7), p.3522-3526

2010

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Prevalence of somatic small fiber neuropathy in obesity

International Journal of Obesity, 2007-02, Vol.31 (2), p.226-235

2007

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Genomic organization of the human thyroglobulin gene: the complete intron-exon structure

European journal of endocrinology, 2001-10, Vol.145 (4), p.485-496

2001

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Growth hormone (GH) treatment reduces peripheral thyroid hormone action in girls with Turner syndrome

Clinical endocrinology (Oxford), 2007-10, Vol.67 (4), p.629-636

2007

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New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

Endocrine reviews, 2010-06, Vol.31 (3), p.396-396

2010

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New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

Endocrinology (Philadelphia), 2010-06, Vol.151 (6), p.2957-2957

2010

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High glucose-mediated loss of cell surface heparan sulfate proteoglycan impairs the endothelial shear stress response

Cytoskeleton (Hoboken, N.J.), 2010-03, Vol.67 (3), p.135-141

2010

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Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter

The Journal of clinical investigation, 1992-10, Vol.90 (4), p.1200-1204

1992

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A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

The journal of clinical endocrinology and metabolism, 1999-07, Vol.84 (7), p.2537-2542

1999

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Control of dendritic cell maturation and function by triiodothyronine

The FASEB journal, 2008-04, Vol.22 (4), p.1032-1042

2008

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Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

Endocrine reviews, 1993-04, Vol.14 (2), p.165-183

1993

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A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger

The journal of clinical endocrinology and metabolism, 1993-07, Vol.77 (1), p.210-215

1993

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A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism

The Journal of clinical investigation, 1991-12, Vol.88 (6), p.1901-1905

1991

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High-level expression and purification of recombinant horseradish peroxidase isozyme C in SF-9 insect cell culture

Process biochemistry (1991), 2005-02, Vol.40 (2), p.795-800

2005

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A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3356-3360

1995

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Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones

The Journal of clinical investigation, 1996-12, Vol.98 (12), p.2838-2844

1996

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Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene

Thyroid (New York, N.Y.), 2001-07, Vol.11 (7), p.685-690

2001

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Genomic organization of the 5' region of the human thyroglobulin gene

European journal of endocrinology, 2000-12, Vol.143 (6), p.789-798

2000

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The field-matching problem as it applies to the peacock three dimensional conformal system for intensity modulation

International journal of radiation oncology, biology, physics, 1996, Vol.34 (1), p.183-187

1996

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A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism

Clinical endocrinology (Oxford), 2011-04, Vol.74 (4), p.533-535

2011

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PCR ANALYSIS OF Y-CHROMOSOME SEQUENCES IN A 45,X MALE PATIENT AND A REVIEW OF THE LITERATURE

Archives of andrology, 2000, Vol.44 (2), p.137-145

2000

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Cytotoxic T lymphocyte antigen 4 heterozygous codon 49 A/G dimorphism is associated to latent autoimmune diabetes in adults (LADA)

Autoimmunity (Chur, Switzerland), 2005-06, Vol.38 (4), p.277-281

2005

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A semi-automated analysis method of small sensory nerve fibers in human skin-biopsies

Journal of neuroscience methods, 2010-01, Vol.185 (2), p.325-337

2010

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Up to date with human thyroglobulin

Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene

New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

Prevalence of somatic small fiber neuropathy in obesity

Genomic organization of the human thyroglobulin gene: the complete intron-exon structure

Growth hormone (GH) treatment reduces peripheral thyroid hormone action in girls with Turner syndrome

New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

New Insights into Thyroglobulin Pathophysiology Revealed by the Study of a Family with Congenital Goiter

High glucose-mediated loss of cell surface heparan sulfate proteoglycan impairs the endothelial shear stress response

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter

A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

Control of dendritic cell maturation and function by triiodothyronine

Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism

High-level expression and purification of recombinant horseradish peroxidase isozyme C in SF-9 insect cell culture

A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis

Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones

Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene

Genomic organization of the 5' region of the human thyroglobulin gene

The field-matching problem as it applies to the peacock three dimensional conformal system for intensity modulation

A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism

PCR ANALYSIS OF Y-CHROMOSOME SEQUENCES IN A 45,X MALE PATIENT AND A REVIEW OF THE LITERATURE

Cytotoxic T lymphocyte antigen 4 heterozygous codon 49 A/G dimorphism is associated to latent autoimmune diabetes in adults (LADA)

A semi-automated analysis method of small sensory nerve fibers in human skin-biopsies

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