Clemens R. Muller

Oberduerrbacher Str. 6
Wuerzburg, BY 97080, Germany

Last Updated: 09/26/2026

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Found 18 publications

Chirality affects biological activity and interactions of azacryptands with alternative DNA structures.

Chirality affects biological activity and interactions of azacryptands with alternative DNA structures.

Journal: Bioorganic chemistry

Published: March 30, 2026

Becker muscular dystrophy (BMD) is caused by a dystrophin missense mutation in the original family of Becker and Kiener.

Becker muscular dystrophy (BMD) is caused by a dystrophin missense mutation in the original family of Becker and Kiener.

Journal: Neuromuscular disorders : NMD

Published: November 06, 2025

Solvation of serine-based model peptides and the role of the intramolecular OH·O hydrogen bond in interpreting VCD spectra.

Solvation of serine-based model peptides and the role of the intramolecular OH·O hydrogen bond in interpreting VCD spectra.

Journal: Physical chemistry chemical physics : PCCP

Published: July 12, 2023

Synthesis and VCD Spectroscopic Characterization of a Series of Azacryptands from a Chiral Valine-Based Derivative of Tris(2-aminoethyl)amine (TREN).

Synthesis and VCD Spectroscopic Characterization of a Series of Azacryptands from a Chiral Valine-Based Derivative of Tris(2-aminoethyl)amine (TREN).

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: July 04, 2023

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

Journal: Human mutation

Published: January 30, 2019

Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication.

Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 20, 2018

BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer.

BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer.

Journal: Breast cancer research : BCR

Published: September 21, 2017

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.

Journal: JAMA oncology

Published: December 30, 2016

Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia.

Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia.

Journal: Neuromuscular disorders : NMD

Published: August 01, 2015

Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype.

Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype.

Journal: European journal of human genetics : EJHG

Published: June 12, 2015

Mini-gene assays confirm the splicing effect of deep intronic variants in the factor VIII gene.

Mini-gene assays confirm the splicing effect of deep intronic variants in the factor VIII gene.

Journal: Thrombosis and haemostasis

Published: May 12, 2015

Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene.

Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene.

Journal: Thrombosis and haemostasis

Published: December 05, 2014

Showing 1-12 of 18

Last Updated: 09/26/2026