A. Grüters

发表

Mutations in the iodotyrosine deiodinase gene and hypothyroidism.

M. Polak, J. Moreno, W. Klootwijk, 2008, The New England journal of medicine.

Modulation of monocarboxylate transporter 8 oligomerization by specific pathogenic mutations.

A. Grüters, H. Biebermann, H. Krude, 2014, Journal of molecular endocrinology.

Endocrine active compounds affect thyrotropin and thyroid hormone levels in serum as well as endpoints of thyroid hormone action in liver, heart and kidney.

A. Grüters, P. J. Hofmann, L. Schomburg, 2004, Toxicology.

Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.

A. Grüters, H. Biebermann, H. Krude, 2007, European journal of endocrinology.

MC4R oligomerizes independently of extracellular cysteine residues

A. Grüters, H. Biebermann, H. Krude, 2006, Peptides.

Functional characterization of the molecular defects causing nephrogenic diabetes insipidus in eight families.

T. Schöneberg, A. Grüters, K. Pasel, 2000, The Journal of clinical endocrinology and metabolism.

Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent.

A. Grüters, H. Biebermann, J. Köhrle, 2009, Journal of molecular endocrinology.

Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.

T. Gudermann, T. Schöneberg, A. Grüters, 1998, The Journal of clinical endocrinology and metabolism.

Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.

T. Gudermann, T. Schöneberg, G. Schultz, 1997, The Journal of clinical endocrinology and metabolism.

A Heterozygous Mutation in the Third Transmembrane Domain Causes a Dominant-Negative Effect on Signalling Capability of the MC4R

J. Hebebrand, A. Hinney, K. Widhalm, 2008, Obesity Facts.

Hypoparathyroidism and Deafness Associated with Pleioplasmic Large Scale Rearrangements of the Mitochondrial DNA: A Clinical and Molecular Genetic Study of Four Children with Kearns-Sayre Syndrome

F. Hanefeld, H. Christen, A. Grüters, 1997, Pediatric Research.

The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiency

R. Rossi, A. Grüters, H. Biebermann, 2009, European journal of endocrinology.

Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist.

K. Clément, A. Grüters, S. Wiegand, 2016, The New England journal of medicine.

Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.

A. Grüters, H. Biebermann, P. Ambrugger, 2001, European journal of endocrinology.

Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency

A. Grüters, H. Biebermann, B. Köhler, 2008, Human mutation.

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

H. Ropers, H. Christen, A. Grüters, 2014, Journal of Medical Genetics.

Implications of Proopiomelanocortin (POMC) Mutations in Humans: The POMC Deficiency Syndrome

A. Grüters, H. Krude, 2000, Trends in Endocrinology & Metabolism.

Rescue of Melanocortin 4 Receptor (MC4R) Nonsense Mutations by Aminoglycoside‐Mediated Read‐Through

J. Hebebrand, A. Hinney, A. Grüters, 2012, Obesity.

Mutationally Induced Disulfide Bond Formation within the Third Extracellular Loop Causes Melanocortin 4 Receptor Inactivation in Patients with Obesity*

T. Schöneberg, A. Grüters, H. Biebermann, 2003, Journal of Biological Chemistry.

Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex development.

A. Grüters, H. Biebermann, H. Krude, 2011, The Journal of clinical endocrinology and metabolism.

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.

A. von Deimling, A. Grüters, H. Biebermann, 2002, The Journal of clinical investigation.

Ring Finger Protein 11 Inhibits Melanocortin 3 and 4 Receptor Signaling

M. Tschöp, A. Grüters, H. Biebermann, 2016, Front. Endocrinol..

Neonatal Thyroid Disorders

A. Grüters, H. Biebermann, H. Krude, 2003, Hormone Research in Paediatrics.

Arteries define the position of the thyroid gland during its developmental relocalisation

S. Mundlos, A. Grüters, H. Krude, 2006, Development.

A role for β-melanocyte-stimulating hormone in human body-weight regulation

M. Tschöp, J. Hebebrand, A. Hinney, 2006 .

Reduced 11beta-hydroxysteroid dehydrogenase type 1 activity in obese boys.

A. Grüters, S. Wiegand, C. Strasburger, 2007, European journal of endocrinology.

False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiency

A. Grüters, J. Hennermann, J. Gellermann, 2009, Journal of Inherited Metabolic Disease.

Mutually opposite signal modulation by hypothalamic heterodimerization of ghrelin- and melanocortin-3 receptors

T. Schöneberg, M. Tschöp, A. Grüters, 2012 .

Mutations in the Human Proopiomelanocortin Gene

A. Grüters, H. Biebermann, H. Krude, 2003, Annals of the New York Academy of Sciences.

A role for b-melanocyte-stimulating hormone in human bodyweight regulation

M. Tschöp, J. Hebebrand, A. Hinney, 2022 .

Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.

M. Polak, A. Grüters, Z. Hochberg, 2011, The Journal of clinical endocrinology and metabolism.

Improving the efficacy of newborn screening for congenital adrenal hyperplasia by adjusting the cut-off level of 17α-hydroxyprogesterone to gestational age

A. Grüters, A. Harras, M. Zachmann, 1994 .

Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood

T. Gudermann, T. Schöneberg, A. Grüters, 2000, Langenbeck's Archives of Surgery.

Alterations of neonatal thyroid function

T. Schöneberg, A. Grüters, H. Biebermann, 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Mutations of the TSH receptor as cause of congenital hyperthyroidism.

R. Paschke, A. Grüters, M. Broecker, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Differential Modulation of Beta-Adrenergic Receptor Signaling by Trace Amine-Associated Receptor 1 Agonists

T. Schöneberg, A. Grüters, H. Biebermann, 2011, PloS one.

Pre- and Postnatal Risk Factors for the Development of Atopy in Childhood

U. Wahn, A. Grüters, W. Luck, 1992 .

Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin.

T. Illig, H. Grallert, J. Hebebrand, 2010, European journal of endocrinology.

Long-Term Monitoring of Treatment with Recombinant Human Growth Hormone by Serial Determinations of Type III Procollagen-Related Antigens in Serum

A. Grüters, T. Danne, D. L'Allemand, 1988, Pediatric Research.

3-iodothyronamine differentially modulates α-2A-adrenergic receptor-mediated signaling.

T. Schöneberg, A. Grüters, H. Biebermann, 2015, Journal of molecular endocrinology.

Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.

W. Arts, A. Grüters, T. Visser, 2007, The Journal of clinical endocrinology and metabolism.

Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural information

A. Grüters, H. Biebermann, H. Krude, 2011, Thyroid research.

G-Protein Coupled Receptor 83 (GPR83) Signaling Determined by Constitutive and Zinc(II)-Induced Activity

M. Tschöp, A. Grüters, H. Biebermann, 2013, PloS one.

V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms

T. Gudermann, T. Schöneberg, G. Schultz, 1998, Human mutation.

Long-term consequences of congenital hypothyroidism in the era of screening programmes.

A. Grüters, H. Krude, A. Jenner, 2002, Best practice & research. Clinical endocrinology & metabolism.

Thyroid hormone transporter defects.

A. Grüters, 2007, Endocrine development.

Molecular description of non-autoimmune hyperthyroidism at a neonate caused by a new thyrotropin receptor germline mutation

A. Grüters, H. Biebermann, H. Krude, 2011, Thyroid research.

A role for beta-melanocyte-stimulating hormone in human body-weight regulation.

A. von Deimling, M. Tschöp, J. Hebebrand, 2006, Cell metabolism.

A. Grüters, B. Köhler, U. Thyen, 2017, Clinical endocrinology.

Title Expanded clinical spectrum in HNF1B-MODY

D. Horn, A. Grüters, E. Klopocki, 2009 .

Hypothalamic and gonadal components of hypogonadism in boys with Prader-Labhart- Willi syndrome.

T. Gasser, V. Rousson, A. Grüters, 2006, The Journal of clinical endocrinology and metabolism.

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

A. Grüters, H. Krude, S. Amselem, 2000, Nature Genetics.

Molecular genetic defects in congenital hypothyroidism.

A. Grüters, H. Biebermann, H. Krude, 2004, European journal of endocrinology.

Severe Congenital Hypothyroidism Due to a Homozygous Mutation of the βTSH Gene

A. Grüters, H. Biebermann, M. Obladen, 1999, Pediatric Research.

Type 2 diabetes and impaired glucose tolerance in European children and adolescents with obesity -- a problem that is no longer restricted to minority groups.

A. Grüters, H. Biebermann, S. Wiegand, 2004, European journal of endocrinology.

Aminoaciduria, but normal thyroid hormone levels and signalling, in mice lacking the amino acid and thyroid hormone transporter Slc7a8.

A. Grüters, J. Köhrle, U. Schweizer, 2011, The Biochemical journal.

Detection and treatment of congenital hypothyroidism

A. Grüters, H. Krude, 2012, Nature Reviews Endocrinology.

Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene.

T. Gudermann, T. Schöneberg, A. Grüters, 1997, The New England journal of medicine.

Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study.

A. Grüters, B. Köhler, U. Thyen, 2012, The Journal of clinical endocrinology and metabolism.

Monocarboxylate transporter 8 deficiency: altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomy.

A. Grüters, H. Krude, M. D. de Angelis, 2011, European journal of endocrinology.

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

A. Grüters, H. Biebermann, H. Krude, 1998, Nature Genetics.

Consensus statement : Childhood obesity

Henry Anhalt, Cecilia Camacho-Hübner, Robert H. Lustig, 2005 .

Endocrine Disruptors and the Thyroid Gland—A Combined in Vitro and in Vivo Analysis of Potential New Biomarkers

A. Grüters, J. Köhrle, B. Radovic, 2007, Environmental health perspectives.

The ultraviolet filter benzophenone 2 interferes with the thyroid hormone axis in rats and is a potent in vitro inhibitor of human recombinant thyroid peroxidase.

A. Grüters, J. Köhrle, C. Hoang‐Vu, 2007, Endocrinology.

Iodine-induced alterations of thyroid function in newborn infants after prenatal and perinatal exposure to povidone iodine.

A. Grüters, D. L'Allemand, P. Heidemann, 1983, The Journal of pediatrics.

Obesity due to proopiomelanocortin deficiency: three new cases and treatment trials with thyroid hormone and ACTH4-10.

A. Grüters, H. Biebermann, H. Krude, 2003, The Journal of clinical endocrinology and metabolism.

Implications of the Phenotype of POMC Deficiency for the Role of POMC‐Derived Peptides in Skin Physiology

A. Grüters, H. Krude, W. Luck, 1999, Annals of the New York Academy of Sciences.

Satisfaction With Genital Surgery and Sexual Life of Adults With XY Disorders of Sex Development: Results From the German Clinical Evaluation Study

A. Grüters, B. Köhler, U. Thyen, 2012 .

Novel insights on thyroid-stimulating hormone receptor signal transduction.

A. Grüters, H. Biebermann, H. Krude, 2013, Endocrine reviews.

Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development.

A. Grüters, H. Biebermann, H. Krude, 2014, European journal of endocrinology.

A Novel Hemizygous Mutation of MAMLD1 in a Patient with 46,XY Complete Gonadal Dysgenesis

A. Grüters, H. Biebermann, H. Krude, 2015, Sexual Development.

Subjective need for psychological support (PsySupp) in parents of children and adolescents with disorders of sex development (dsd)

A. Grüters, B. Köhler, U. Thyen, 2015, European Journal of Pediatrics.

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans

G. Kokai, A. Grüters, M. Wlodarski, 2017, The Journal of clinical investigation.

Autosomal-dominant mode of inheritance of a melanocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a dominant-negative effect caused by receptor dimerization.

T. Gudermann, A. Grüters, H. Biebermann, 2003, Diabetes.

Is there a further acceleration in the age at onset of menarche? A cross-sectional study in 1840 school children focusing on age and bodyweight at the onset of menarche.

A. Grüters, S. Wiegand, H. Krude, 2009, European journal of endocrinology.

Molecular Pathogenesis of Neonatal Hypothyroidism

A. Grüters, H. Biebermann, H. Krude, 2000, Hormone Research in Paediatrics.

MC4R agonism promotes durable weight loss in patients with leptin receptor deficiency

K. Clément, A. Grüters, H. Biebermann, 2018, Nature Medicine.

Essential Molecular Determinants for Thyroid Hormone Transport and First Structural Implications for Monocarboxylate Transporter 8*

A. Grüters, J. Köhrle, G. Krause, 2010, The Journal of Biological Chemistry.

Neuronal 3′,3,5-Triiodothyronine (T3) Uptake and Behavioral Phenotype of Mice Deficient in Mct8, the Neuronal T3 Transporter Mutated in Allan–Herndon–Dudley Syndrome

H. Fuchs, W. Wurst, A. Grüters, 2009, The Journal of Neuroscience.

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

Luca Chiovato, P. Macchia, R. Lauro, 1998, Nature Genetics.

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

A. Grüters, H. Biebermann, H. Krude, 2014, The Journal of clinical endocrinology and metabolism.

Mutations in TITF-1 are associated with benign hereditary chorea.

B. D. de Vries, M. MacDonald, W. Arts, 2002, Human molecular genetics.

Congenital Central Hypothyroidism due to Homozygous Thyrotropin β 313ΔT Mutation Is Caused by a Founder Effect

A. Pfeufer, A. Grüters, H. Biebermann, 2002 .

A New Multisystem Disorder Caused by the G&agr;s Mutation p.F376V

M. Dattani, A. Grüters, H. Biebermann, 2018, The Journal of clinical endocrinology and metabolism.

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Wei Chen, S. Lenzner, H. Ropers, 2007, Human Genetics.

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency.

A. Grüters, H. Krude, V. Tardy, 2000, The Journal of clinical endocrinology and metabolism.

A new multi-system disorder caused by the Gαs mutation p.F376V

M. Dattani, A. Grüters, H. Biebermann, 2018 .

Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect.

A. Pfeufer, A. Grüters, H. Biebermann, 2002, The Journal of clinical endocrinology and metabolism.

Ocular manifestations in children and adolescents with thyrotoxicosis.

A. Grüters, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The prevalence of anti-thyroid peroxidase antibodies and autoimmune thyroiditis in children and adolescents in an iodine replete area.

A. Grüters, H. Willgerodt, B. Ehnert, 2003, European journal of endocrinology.

Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? The Impact of Cryptic Relatedness

T. Illig, H. Grallert, J. Hebebrand, 2012, Hormone Research in Paediatrics.

Identification of the Translation Start Site of the Human Melanocortin 3 Receptor

A. Grüters, H. Biebermann, A. Rediger, 2012, Obesity Facts.

Treatment of Graves’ Disease in Children and Adolescents

A. Grüters, 1998, Hormone Research in Paediatrics.

Expanded clinical spectrum in hepatocyte nuclear factor 1b-maturity-onset diabetes of the young.

D. Horn, A. Grüters, E. Klopocki, 2009, The Journal of clinical endocrinology and metabolism.

HNF1B Abnormality (Mature-Onset Diabetes of the Young 5) in Children and Adolescents

D. Horn, A. Grüters, E. Klopocki, 2008, Diabetes Care.

Angeborene Hypothyreose

A. Grüters, H. Krude, 2008, Monatsschrift Kinderheilkunde.

Cytotoxic antibodies in congenital hypothyroidism.

A. Grüters, U. Bogner, H. Schleusener, 1989, The Journal of clinical endocrinology and metabolism.

Guidelines for neonatal screening programmes for congenital hypothyroidism

A. Grüters, F. Delange, O. Hníková, 1993, European Journal of Pediatrics.

Results of the screening program for congenital hypothyroidism in Berlin (1978-1995).

A. Grüters, E. Pfeiffer, U. Lehmkuhl, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The Use of L-T4 as Liquid Solution Improves the Practicability and Individualized Dosage in Newborns and Infants with Congenital Hypothyroidism

A. Grüters, H. Krude, D. L'Allemand, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

The Interdisciplinary Diagnosis of Rare Diseases-Results of the Translate-NAMSE Project.

M. Nöthen, S. Mundlos, T. Meitinger, 2022, Deutsches Arzteblatt international.

The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidism.

T. Gudermann, T. Schöneberg, A. Grüters, 2001, The Journal of clinical endocrinology and metabolism.

The relevance of genetic susceptibility in Graves' disease and immune thyroiditis.

A. Grüters, W. Mayr, U. Bogner, 2009, Experimental and clinical endocrinology.

Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity.

P. Dominguez-Salas, A. Prentice, F. Heppner, 2016, Cell metabolism.

Gender-specific differences of serum leptin in obese and normal-weight adolescents: studies in type-I diabetes and Turner syndrome.

A. Grüters, T. Danne, B. Mayr, 1997, Hormone research.

Associations between body mass, leptin, IGF-I and circulating adrenal androgens in children with obesity and premature adrenarche.

T. Gasser, G. Brabant, V. Rousson, 2002, European journal of endocrinology.

Thyroid Function and Obesity in Children and Adolescents

A. Grüters, D. L'Allemand, H. Stichel, 2001, Hormone Research in Paediatrics.

Mean High-Dose L-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital Hypothyroidism

A. Grüters, H. Krude, M. Craig, 2018, The Journal of clinical endocrinology and metabolism.

Heterodimerization of Hypothalamic G-Protein-Coupled Receptors Involved in Weight Regulation

A. Grüters, H. Biebermann, H. Krude, 2009, Obesity Facts.

Metformin and placebo therapy both improve weight management and fasting insulin in obese insulin-resistant adolescents: a prospective, placebo-controlled, randomized study.

A. Grüters, S. Wiegand, H. Krude, 2010, European journal of endocrinology.

Diagnostic Tests of Thyroid Function in Children and Adolescents

A. Grüters, 2003 .

Earliest prevention of endemic goiter by iodine supplementation during pregnancy.

W. Göpel, A. Grüters, U. Bogner, 1996, European journal of endocrinology.

Maternal Thyroid Autoantibodies and Fetal Thyroid Growth

A. Grüters, U. Bogner, P. Schumm-Draeger, 1992 .

Small thyroid volumes and normal iodine excretion in Berlin schoolchildren indicate full normalization of iodine supply.

A. Grüters, H. Willgerodt, B. Stach, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

A new phenotype of nongoitrous and nonautoimmune hyperthyroidism caused by a heterozygous thyrotropin receptor mutation in transmembrane helix 6.

A. Grüters, H. Biebermann, H. Krude, 2010, The Journal of clinical endocrinology and metabolism.

Incidence of iodine contamination in neonatal transient hyperthyrotropinemia

A. Grüters, D. L'Allemand, P. Heidemann, 1983, European Journal of Pediatrics.

Update on the Management of Congenital Hypothyroidism

A. Grüters, H. Krude, 2007, Hormone Research in Paediatrics.

[Study of antibody-dependent cell mediated cytotoxicity and thyroid growth blocking antibodies in congenital hypothyroidism].

A. Grüters, U. Bogner, M. Dugué, 1991, Archives francaises de pediatrie.

Prospective study on the atopy preventive effect of maternal avoidance of milk and eggs during pregnancy and lactation

U. Wahn, A. Grüters, A. Coumbos, 1996, European Journal of Pediatrics.

Aminoglycoside pretreatment partially restores the function of truncated V(2) vasopressin receptors found in patients with nephrogenic diabetes insipidus.

K. Sangkuhl, T. Schöneberg, G. Schultz, 2002, The Journal of clinical endocrinology and metabolism.

Relationship of procollagen type III propeptide-related antigens in serum to somatic growth in healthy children and patients with growth disorders.

D. Schuppan, A. Grüters, T. Danne, 1989, The Journal of pediatrics.

MC4R Dimerization in the Paraventricular Nucleus and GHSR/MC3R Heterodimerization in the Arcuate Nucleus: Is There Relevance for Body Weight Regulation?

M. Tschöp, A. Grüters, H. Biebermann, 2012, Neuroendocrinology.

Effect of different oestrogen doses on final height reduction in girls with constitutional tall stature

A. Grüters, P. Heidemann, H. Helge, 1989, European Journal of Pediatrics.

Mutually Opposite Signal Modulation by Hypothalamic Heterodimerization of Ghrelin and Melanocortin-3 Receptors*

T. Schöneberg, M. Tschöp, A. Grüters, 2011, The Journal of Biological Chemistry.

Transition for adolescents with a rare disease: results of a nationwide German project

A. Grüters, H. Krude, F. Hauck, 2023, Orphanet Journal of Rare Diseases.

Severe hypokalaemia due to hyperreninaemia and secondary hyperaldosteronism in a boy with pheochromocytoma

W. Göpel, A. Grüters, D. Schnabel, 1996, European Journal of Pediatrics.

Inhibition of melanocortin-4 receptor dimerization by substitutions in intracellular loop 2.

A. Grüters, H. Biebermann, H. Krude, 2013, Journal of molecular endocrinology.

New pathogenic thyrotropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCR.

A. Grüters, B. Wiesner, H. Biebermann, 2012, The Journal of clinical endocrinology and metabolism.

Evolutionary aspects in evaluating mutations in the melanocortin 4 receptor.

Thomas Gudermann, Torsten Schöneberg, T. Gudermann, 2007, Endocrinology.

Inverse Agonistic Action of 3-Iodothyronamine at the Human Trace Amine-Associated Receptor 5

T. Schöneberg, M. Tschöp, A. Grüters, 2015, PloS one.

Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1

H. Völzke, G. Homuth, A. Teumer, 2017, Front. Pharmacol..

Etiological grouping of permanent congenital hypothyroidism with a thyroid gland in situ.

A. Grüters, H. Krude, R. Finke, 1994, Hormone research.

A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G‐protein coupling

T. Gudermann, T. Schöneberg, G. Schultz, 1998, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathy.

A. Grüters, B. Köhler, B. Royer-Pokora, 2001, The Journal of pediatrics.

Iodine in Contrast Agents and Skin Disinfectants Is the Major Cause for Hypothyroidism in Premature Infants during Intensive Care

A. Grüters, B. Weber, P. Beyer, 1987 .

Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism

A. Grüters, H. Biebermann, H. Krude, 1997, Experimental and clinical endocrinology & diabetes.

The extracellular N-terminal domain of G-protein coupled receptor 83 regulates signaling properties and is an intramolecular inverse agonist

M. Tschöp, A. Grüters, H. Biebermann, 2014, BMC Research Notes.

Contents Vol. 77, 2012

F. Kronenberg, V. Tillmann, T. Stijnen, 2012, Hormone Research in Paediatrics.

2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism

G. Brabant, E. Fliers, M. Dattani, 2018, European Thyroid Journal.

Bilateral Wilms Tumor in a Boy with Severe Hypospadias and Cryptorchidism Due to a Heterozygous Mutation in the WT1 Gene

A. Grüters, B. Köhler, B. Royer-Pokora, 1999, Pediatric Research.

Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years.

A. Grüters, H. Biebermann, B. Köhler, 1996, The Journal of clinical endocrinology and metabolism.

The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis

W. Göpel, A. Grüters, H. Biebermann, 2009, Experimental and clinical endocrinology & diabetes.