UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Up to date with human thyroglobulin

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

2001

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2000

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Control of dendritic cell maturation and function by triiodothyronine

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

2008

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

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

1993

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Defective Organification of Iodide Causing Hereditary Goitrous Hypothyroidism

Thyroid (New York, N.Y.), 1993, Vol.3 (2), p.143-159

1993

Volltextzugriff (PDF)

Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

Clinical chemistry (Baltimore, Md.), 2006-02, Vol.52 (2), p.182-191

2006

Volltextzugriff (PDF)

Genomic Organization of the 3′ Region of the Human Thyroglobulin Gene

Thyroid (New York, N.Y.), 1999-09, Vol.9 (9), p.93-912

1999

Volltextzugriff (PDF)

Molecular analysis of sex determination in sex-reversed and true hermaphroditism

Brazilian journal of medical and biological research, 1996-06, Vol.29 (6), p.743

1996

Volltextzugriff (PDF)

Abnormal H2O2 supply in the thyroid of a patient with goiter and iodine organification defect

The journal of clinical endocrinology and metabolism, 1987-08, Vol.65 (2), p.344-348

1987

Volltextzugriff (PDF)

Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis

Brazilian journal of medical and biological research, 1994-12, Vol.27 (12), p.2745

1994

Volltextzugriff (PDF)

1 – 25 von 80

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(54)

Publikationsform

Artikel
(80)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(57)
Science & Technology
(53)
Life Sciences & Biomedicine
(52)
Endocrinology & Metabolism
(30)
Thyroglobulin - Genetics
(30)
Male
(27)
Biological And Medical Sciences
(26)
Female
(23)
Goiter - Genetics
(23)
Molecular Sequence Data
(23)
Medical Sciences
(20)
Adult
(18)
Base Sequence
(18)
Amino Acid Sequence
(16)
Animals
(15)
Endocrinopathies
(15)
Hypothyroidism - Genetics
(14)
Polymerase Chain Reaction
(14)
Thyroid. Thyroid Axis
(14)
Fundamental And Applied Biological Sciences. Psychology
(13)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Up to date with human thyroglobulin

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

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

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

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

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

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

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

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

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

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

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

Control of dendritic cell maturation and function by triiodothyronine

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

Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

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

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

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

Defective Organification of Iodide Causing Hereditary Goitrous Hypothyroidism

Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

Genomic Organization of the 3′ Region of the Human Thyroglobulin Gene

Molecular analysis of sex determination in sex-reversed and true hermaphroditism

Abnormal H2O2 supply in the thyroid of a patient with goiter and iodine organification defect

Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis

Suchergebnisse filtern