Missense variation of the CFTR gene codon 507

The interplay of chronic stress and genetic traits discriminates between patients suffering from multisomatoform disorder with pain as the leading symptom and matched controls.

Journal of affective disorders·2022

[CF Lung Disease - a German S3 Guideline: Module 2: Diagnostics and Treatment in Chronic Infection with Pseudomonas aeruginosa].

Pneumologie (Stuttgart, Germany)·2018

Hereditary hemorrhagic telangiectasia: A Case Report.

Saudi medical journal·2016

The potential benefits of genetic testing in breast and ovarian cancer.

Saudi medical journal·2016

Erratum to "Practical guidelines: lung transplantation in patients with cystic fibrosis".

Pulmonary medicine·2015

[Concepts for the return of secondary genetic findings in medical diagnostics and research].

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz·2014

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Human mutation·2026

Mutation-Immune Crosstalk Contextualizes CAF-Associated ARPC1A Programs and Cisplatin Response in Gastric Cancer.

Human mutation·2026

Identification of Novel Pathogenic Variants in Familial Adenomatous Polyposis Through Whole Genome Sequencing.

Human mutation·2026

A Pathogenic ANK1 c.5096G>A Mutation Disrupting the Ankyrin-1/β-Spectrin Interaction in Hereditary Spherocytosis.

Human mutation·2026

A Novel Splice Variant in the COL1A1 Gene Leads to Exon 46 Skipping and Osteogenesis Imperfecta.

Human mutation·2026

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Human mutation·2026

Toward Personalized Psychotherapy in Anorexia Nervosa: Evidence from Long-Term Moderator Analyses of the ANTOP study.

Psychotherapy and psychosomatics·2026

Mindful Eating, Disordered Eating, and Exercise Addiction: A Bayesian Gaussian Network Analysis.

Nutrients·2026

Preliminary testing of a prespecified liability architecture for autism: theory-guided pathogenetic triad models outperform strength-matched alternatives.

Frontiers in psychiatry·2026

Behavioral Complexity in Alzheimer's Disease: A Diversity-Based Analysis of Neuropsychiatric Symptoms.

Brain sciences·2026

Unique environmental and familial influence on amygdalar hyperresponsivity in post-traumatic stress disorder - a discordant monozygotic twin study.

Biological psychiatry·2026

The Wistar-Kyoto rat as a model relevant to inattentive ADHD: substrain variability and affective comorbidity.

Pharmacological reports : PR·2026

Related Experiment Videos

Missense variation of the CFTR gene codon 507

Related Concept Videos

The interplay of chronic stress and genetic traits discriminates between patients suffering from multisomatoform disorder with pain as the leading symptom and matched controls.

[CF Lung Disease - a German S3 Guideline: Module 2: Diagnostics and Treatment in Chronic Infection with Pseudomonas aeruginosa].

Hereditary hemorrhagic telangiectasia: A Case Report.

The potential benefits of genetic testing in breast and ovarian cancer.

Erratum to "Practical guidelines: lung transplantation in patients with cystic fibrosis".

[Concepts for the return of secondary genetic findings in medical diagnostics and research].

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Mutation-Immune Crosstalk Contextualizes CAF-Associated ARPC1A Programs and Cisplatin Response in Gastric Cancer.

Identification of Novel Pathogenic Variants in Familial Adenomatous Polyposis Through Whole Genome Sequencing.

A Pathogenic ANK1 c.5096G>A Mutation Disrupting the Ankyrin-1/β-Spectrin Interaction in Hereditary Spherocytosis.

A Novel Splice Variant in the COL1A1 Gene Leads to Exon 46 Skipping and Osteogenesis Imperfecta.

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Toward Personalized Psychotherapy in Anorexia Nervosa: Evidence from Long-Term Moderator Analyses of the ANTOP study.

Mindful Eating, Disordered Eating, and Exercise Addiction: A Bayesian Gaussian Network Analysis.

Preliminary testing of a prespecified liability architecture for autism: theory-guided pathogenetic triad models outperform strength-matched alternatives.

Behavioral Complexity in Alzheimer's Disease: A Diversity-Based Analysis of Neuropsychiatric Symptoms.

Unique environmental and familial influence on amygdalar hyperresponsivity in post-traumatic stress disorder - a discordant monozygotic twin study.

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Related Experiment Videos

Missense variation of the CFTR gene codon 507

Related Concept Videos

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