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01

Wide spectral association study in obesity patients: endemic diversity, pharmaceuticals, and a comprehensive SNV and CNV approach utilizing high-throughput bead chip microarray technology.

02

Pharmacodynamics and Pharmacokinetics properties of 5-fluorouracil from genomics view, case control association study utilizing bead chip microarray technology; a comprehensive SNV and CNV approach of hotspot clusters

03

A retrospective Association case control study in epilepsy patients; Comprehensive SNV and CNV approach based on the RWE data analysis

04

Create and validating cornea invitro model with its associated regenerative characterization algorithm

05

CTCF and its epigenomic, genomics, and proteomics implications on regulating cancer associated genes; a multi-omics approach

06

A retrospective Association case control study in CAD patients; Comprehensive SNV and CNV approach based on the RWE data analysis

07

A multi-omics approach in autism spectrum disorder, A multidisciplinary GWAS and EWAS cohort 

08

Programmed mRNA loaded matrix for the purpose of wound healing; a new horizons in wound managements

09

High Trough-put chromosome capture analysis tool, A new approach for comperative epigenome studies

10

Stop Codon Skipping by medicine re-adjustment approaches, case experimental series

11

Golden Gate approach in gene treatments, ALS, Alport and Limb Girdle Disorders

HAKKIMIZDA >

Türkiye'de genetik bozukluk araştırmalarının önde gelen topluluklarından birine hoş geldiniz. Genetik Bozukluklar Araştırma ve Tedavi Derneği olan RTSGD, teşhis, tedavi ve destek hizmetlerinde öncü gelişmelere kendini adamıştır. Farkındalığı artırma, işbirliğini teşvik etme ve hastalar, aileler ve profesyoneller için eğitim sağlama misyonumuz hakkında bilgi edinin.

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