Search Results - Annette Grüters
- Showing 1 - 20 results of 38
- Go to Next Page
-
1
-
2
-
3
-
4
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 Di... by Heike Biebermann, Heiko Krude, Andrea Elsner, Vladimir Chubanov, Thomas Gudermann, Annette Grüters
Published 2003Artigo -
5
-
6
-
7
-
8
-
9
-
10
-
11
-
12
Aminoaciduria, but normal thyroid hormone levels and signalling, in mice lacking the amino acid and thyroid hormone transporter <i>Slc7a8</i> by Doreen Braun, Eva K. Wirth, Franziska Wohlgemuth, Nathalie Reix, Marc Klein, Annette Grüters, Josef Köhrle, Ulrich Schweizer
Published 2011Artigo -
13
-
14
Differential Modulation of Beta-Adrenergic Receptor Signaling by Trace Amine-Associated Receptor 1 Agonists by Gunnar Kleinau, Juliane Pratzka, Daniela Nürnberg, Annette Grüters, Dagmar Führer‐Sakel, Heiko Krude, Josef Köhrle, Torsten Schöneberg, Heike Biebermann
Published 2011Artigo -
15
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 domina... by Eva Al Taji, Heike Biebermann, Z Límanová, O Hníková, Jaroslav Zikmund, Christof Dame, Annette Grüters, Jan Lebl, Heiko Krude
Published 2007Artigo -
16
Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis by Peter Kühnen, Serap Turan, Sebastian Fröhler, Tülay Güran, Saygın Abalı, Heike Biebermann, Abdullah Bereket, Annette Grüters, Wei Chen, Heiko Krude
Published 2013Artigo -
17
-
18
The prevalence of anti-thyroid peroxidase antibodies and autoimmune thyroiditis in children and adolescents in an iodine replete area by M Kabelitz, KP Liesenkötter, Barbara Stach, H Willgerodt, W Stablein, W Singendonk, Elke Jäger‐Roman, H Litzenborger, B Ehnert, Annette Grüters
Published 2003Artigo -
19
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 insuffici... by Birgit Köhler, Lin Lin, Inas Mazen, Cigdem Cetindag, Heike Biebermann, Ilker Akkurt, Rainer Rossi, Olaf Hiort, Annette Grüters, John C. Achermann
Published 2009Artigo -
20
Search Tools:
Related Subjects
Medicine
Biology
Endocrinology
Internal medicine
Gene
Genetics
Thyroid
Mutation
Phenotype
Missense mutation
Receptor
Chemistry
Biochemistry
Pediatrics
Cell biology
Hormone
Melanocortin
Congenital hypothyroidism
Obesity
Psychiatry
Signal transduction
Disorders of sex development
Haploinsufficiency
Melanocortin receptor
Transporter
Agonist
Anatomy
Diabetes mellitus
G protein-coupled receptor
Gastroenterology