Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Carriage of Non-Functional Allelic Variant T (rs2069522) of the CYP1A2 Gene in a Patient with Recurrent Depressive Disorder and Therapy Resistance - Clinical Case.

Psychiatria Danubina - 1 Oct 2023

Strelnik Anna, Sheyfer Mikhail, Izmailova Olga, Shnayder Natalia, Zhuravlev Nikita, Otmakhov Andrey, Nasyrova Regina

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Cytochrome P-450 CYP1A2
Share to Depressive Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Polymorphism, Genetic

Share to Polymorphism, Single Nucleotide

Share to Recurrence

Source

Identifiers

PMID: 37800261

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Carriage of Non-Functional Allelic Variant T (rs2069522) of the CYP1A2 Gene in a Patient with Recurrent Depressive Disorder and Therapy Resistance - Clinical Case.PMID 37800261Read ↗

Five novel natural allelic variants-951A>C, 1042G>A (D348N), 1156A>T (I386F), 1217G>A (C406Y) and 1291C>T (C431Y)-of the human CYP1A2 gene in a French Caucasian population.Semantic proximity Read ↗

Non-response to consecutive antidepressant therapy caused by CYP2D6 ultrarapid metabolizer phenotype.Semantic proximity Read ↗

Single nucleotide polymorphism in the drug transporter gene ABCB1 in treatment-resistant depression: clinical practice.Semantic proximity Read ↗

Common variants in SLC6A2, SLC6A3, DRD2, and major depressive disorder: an association study in the Chinese Han population.Semantic proximity Read ↗

Development of a high throughput single nucleotide polymorphism screening method for the cytochrome P450 1A2 polymorphisms CYP1A2*1C and CYP1A2*1F: are they useful as predictive markers in mental disorders?Semantic proximity Read ↗

Does G2677T Polymorphism of the MDR1 Gene Make a Difference in the Therapeutic Response to Paroxetine in Depressed Patients in a Slovakian Population?Semantic proximity Read ↗

Serotonin transporter gene polymorphisms and treatment-resistant depression.Semantic proximity Read ↗

Association study of GRM7 polymorphisms with major depressive disorder in the Chinese Han population.Semantic proximity Read ↗

The Influence of C3435T Polymorphism of the ABCB1 Gene on Genetic Susceptibility to Depression and Treatment Response in Polish Population - Preliminary Report.Semantic proximity Read ↗

Frequency of "Poor Transporter" Phenotype Among Patients with Mental Disorders: Pilot StudySemantic proximity Read ↗

Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder.Semantic proximity Read ↗

ABCB1 C1236T, G2677TA and C3435T Genetic Polymorphisms and Antidepressant Response Phenotypes: Results from a Portuguese Major Depressive Disorder Cohort.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.