You are currently viewing a new version of our website. To view the old version click .

Genes, Volume 13, Issue 12

December 2022 - 241 articles

Cover Story: Clostridioides difficile is an obligate anaerobic pathogen that is among the most common causes of healthcare-associated infections. It poses a global threat due to the clinical outcomes of infection and resistance to antibiotics recommended by international guidelines for its eradication. In particular, C. difficile infection can lead to fulminant colitis associated with shock, hypotension, megacolon, and, in severe cases, death. It is therefore of the utmost urgency to fully characterize this pathogen and to better understand its spread, in order to reduce infection rates and improve therapy success. Our work focuses on the genetic evolution of C. difficile virulence, antimicrobial resistance, the molecular typing techniques used to characterize this pathogen, the global distribution of the most common ribotypes, and novel genetic engineering strategies to control this threat. View this paper
  • Issues are regarded as officially published after their release is announced to the table of contents alert mailing list .
  • You may sign up for email alerts to receive table of contents of newly released issues.
  • PDF is the official format for papers published in both, html and pdf forms. To view the papers in pdf format, click on the "PDF Full-text" link, and use the free Adobe Reader to open them.

Articles (241)

  • Article
  • Open Access
3 Citations
2,072 Views
11 Pages

17 December 2022

The Tibetan pig is an endemic economic animal in the plateau region of China, and has a unique adaptation mechanism to the plateau hypoxic environment. Research into microRNAs (miRNAs) involved in the mechanism underlying hypoxia adaptation of Tibeta...

  • Article
  • Open Access
5 Citations
4,811 Views
15 Pages

Folic Acid and Vitamin B12 Prevent Deleterious Effects of Rotenone on Object Novelty Recognition Memory and Kynu Expression in an Animal Model of Parkinson’s Disease

  • Gabriela Canalli Kretzschmar,
  • Adriano D. S. Targa,
  • Sheila Coelho Soares-Lima,
  • Priscila Ianzen dos Santos,
  • Lais S. Rodrigues,
  • Daniel A. Macedo,
  • Luis Felipe Ribeiro Pinto,
  • Marcelo M. S. Lima and
  • Angelica Beate Winter Boldt

17 December 2022

Parkinson’s disease (PD) is characterized by a range of motor signs, but cognitive dysfunction is also observed. Supplementation with folic acid and vitamin B12 is expected to prevent cognitive impairment. To test this in PD, we promoted a lesi...

  • Article
  • Open Access
2 Citations
1,852 Views
14 Pages

Identification of Reliable Reference Genes under Different Stresses and in Different Tissues of Toxicodendron succedaneum

  • Dongxiao Ma,
  • Qin Zhang,
  • Jintao Zhou,
  • Yu Lu,
  • Xiaomeng Duan,
  • Chengzhong He and
  • Jinde Yu

17 December 2022

Toxicodendron succedaneum (L.) Kuntze (T. succedaneum) is an economic tree species that produces urushiol and urushi wax, and it is of great value in industry and medicine. However, the stability of reference genes (RGs) has not been systematically r...

  • Article
  • Open Access
5 Citations
2,665 Views
19 Pages

Genome-Wide Identification of Common Bean PvLTP Family Genes and Expression Profiling Analysis in Response to Drought Stress

  • Xue Dong,
  • Huijun Zhu,
  • Xiaopeng Hao,
  • Yan Wang,
  • Xiaolei Ma,
  • Jiandong Zhao and
  • Jianwu Chang

16 December 2022

Common bean is one of the most important legume crops for human consumption. Its yield is adversely affected by environmental stress. Plant non-specific lipid transfer proteins (nsLTPs) are essential for plant growth, development, and resistance to a...

  • Article
  • Open Access
3 Citations
4,177 Views
22 Pages

A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility

  • Federica Esposito,
  • Ana Maria Osiceanu,
  • Melissa Sorosina,
  • Linda Ottoboni,
  • Bryan Bollman,
  • Silvia Santoro,
  • Barbara Bettegazzi,
  • Andrea Zauli,
  • Ferdinando Clarelli and
  • Elisabetta Mascia
  • + 18 authors

16 December 2022

While the role of common genetic variants in multiple sclerosis (MS) has been elucidated in large genome-wide association studies, the contribution of rare variants to the disease remains unclear. Herein, a whole-genome sequencing study in four affec...

  • Article
  • Open Access
3 Citations
4,104 Views
13 Pages

16 December 2022

With the development of high-throughput sequencing, RNA sequencing has been widely used in the identification of candidate genes for complex traits in livestock, and the functional genes and mutations with large genetic effects on milk production tra...

  • Article
  • Open Access
5 Citations
3,211 Views
16 Pages

Diagnostic and Prognostic Risk Assessment of Heat Shock Protein HSPA1B rs2763979 Gene Variant in Asthma

  • Salwa Faisal,
  • Sherouk Abdelaal,
  • Mohammed A. Jeraiby,
  • Fatihi Hassan Soliman Toaimah,
  • Shahad W. Kattan,
  • Abdelhady Ragab Abdel-Gawad,
  • Eman Riad,
  • Eman A. Toraih,
  • Manal S. Fawzy and
  • Ahmed Ibrahim

16 December 2022

Given the significant role the heat shock protein Hsp70 plays in modulating cellular homeostasis in several chronic inflammatory disorders, the genetic variation of the inducible HSP70 (HSPA1B) gene may impact protein expression and disease phenotype...

  • Review
  • Open Access
31 Citations
12,696 Views
21 Pages

53BP1: Keeping It under Control, Even at a Distance from DNA Damage

  • Emilie Rass,
  • Simon Willaume and
  • Pascale Bertrand

16 December 2022

Double-strand breaks (DSBs) are toxic lesions that can be generated by exposure to genotoxic agents or during physiological processes, such as during V(D)J recombination. The repair of these DSBs is crucial to prevent genomic instability and to maint...

  • Article
  • Open Access
6 Citations
2,819 Views
11 Pages

Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies

  • Seher Basaran,
  • Recep Has,
  • Ibrahim Halil Kalelioglu,
  • Tugba Sarac Sivrikoz,
  • Birsen Karaman,
  • Melike Kirgiz,
  • Tahir Dehgan,
  • Tugba Kalayci,
  • Bilge Ozsait Selcuk and
  • Peter Miny
  • + 1 author

16 December 2022

The scope of cell-free DNA (cfDNA) testing was expanded to the genome, which allowed screening for rare chromosome anomalies (RCAs). Since the efficiency of the test for RCAs remains below the common aneuploidies, there is a debate on the usage of ex...

  • Review
  • Open Access
91 Citations
14,123 Views
23 Pages

Genetic and Epigenetic Etiology of Inflammatory Bowel Disease: An Update

  • Sara Jarmakiewicz-Czaja,
  • Magdalena Zielińska,
  • Aneta Sokal and
  • Rafał Filip

16 December 2022

Inflammatory bowel disease (IBD) is a chronic disease with periods of exacerbation and remission of the disease. The etiology of IBD is not fully understood. Many studies point to the presence of genetic, immunological, environmental, and microbiolog...

of 25

Get Alerted

Add your email address to receive forthcoming issues of this journal.

XFacebookLinkedIn
Genes - ISSN 2073-4425