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Ralph Röth

Medizinisch-technischer Assistent

Name	Ralph Röth
Ort	Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dipl.-Ing.
Beruf	Medizinisch-technischer Assistent (charakteristischer Beruf)
Variante	R. Röth Ralf Roeth Ralph Roeth
Beziehung	Universität Heidelberg. Institut für Humangenetik
Datensatztyp	Person
GND-Nummer	1068410221
Datensatz-ID	1068410221
Beteiligt an alle anzeigen Targeted proteomics reveals quantitative differences in low-abundance glycosyltransferases of patients with congenital disorders of glycosylation Cargo and Functional Profile of Saliva-Derived Exosomes Reveal Biomarkers Specific for Head and Neck Cancer Comparison of plasma- and saliva-derived exosomal miRNA profiles reveals diagnostic potential in head and neck cancer Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature miR-16 and miR-103 impact 5-HT4 receptor signalling and correlate with symptom profile in irritable bowel syndrome Impact of Altered WNT2B Expression on Bladder Wall Fibroblasts: Implications for Apoptosis Regulation in the Stroma of the Lower Urinary Tract Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency

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Ralph Röth

Targeted proteomics reveals quantitative differences in low-abundance glycosyltransferases of patients with congenital disorders of glycosylation

Cargo and Functional Profile of Saliva-Derived Exosomes Reveal Biomarkers Specific for Head and Neck Cancer

Comparison of plasma- and saliva-derived exosomal miRNA profiles reveals diagnostic potential in head and neck cancer

Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes

Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism

Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism

Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature

miR-16 and miR-103 impact 5-HT4 receptor signalling and correlate with symptom profile in irritable bowel syndrome

Impact of Altered WNT2B Expression on Bladder Wall Fibroblasts: Implications for Apoptosis Regulation in the Stroma of the Lower Urinary Tract

Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation

Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency