Volume6, Issue0 (2022)

Journal of Translational Genetics and Genomics

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Journal of Translational Genetics and Genomics

ISSN 2578-5281 (Online)

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Volume

Table of Contents (28 articles)

The endocrine and epigenetic impact of persistent cow milk consumption on prostate carcinogenesis

In vitro modeling of the complex retinal condition age-related macular degeneration

Multiple myeloma etiology and treatment

Identification of molecular signatures and pathways of obese breast cancer gene expression data by a machine learning algorithm

Zebrafish models of inherited retinal dystrophies

Gene editing treatment strategies for retinitis pigmentosa assessed in Xenopus laevis carrying a mutant Rhodopsin allele

Alternative isoforms of RNA polymerase III impact the non-coding RNA transcriptome, viability, proliferation and differentiation of prostate cancer cells

Clinical significance of aetiological heterogeneity in classical Hodgkin lymphoma

Enigmatic role of WRN-RECQL helicase in DNA repair and its implications in cancer

Roles of gut dysbiosis, anti-proliferative proteins, and post-transcriptional regulation in carcinogenesis

Epilepsy and electroencephalography in Pitt-Hopkins syndrome

Stem cell-based therapy for myopic maculopathy: a new concept

The DNA damage response - from cell biology to human disease

Genetic predisposition to obesity and inflammation in a tri-racial/ethnic breast cancer population

Transcriptomics insights into interpreting AMD-GWAS discoveries for biological and clinical applications

Clinical characterization of a new individual with mild SC4MOL deficiency: diagnostic and therapeutic implications

Estrogen and DNA damage modulate mRNA levels of genes involved in homologous recombination repair in estrogen-deprived cells

Potential therapeutic response in a severe case of autosomal dominant osteopetrosis type I

Potentials and challenges of launching the pilot phase of Hong Kong Genome Project

Neurogenic dysphagia: current pharmacogenomic perspectives

Diagnostic strategies in patients with undiagnosed and rare diseases

Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease

NUT midline carcinoma presenting initially as thyroid cancer: a case report and review of treatment

The many roles of the Alzheimer-associated gene PM20D1

Development and early evaluation of clinical decision support for long QT syndrome population screening

Genetic risk and its role in primary prevention of CAD

Rationale for haploinsufficiency correction therapy in neurofibromatosis type 1

The importance of genetics in an advanced integrative model of autism spectrum disorder

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Committee on Publication Ethics

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Committee on Publication Ethics

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