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Genes, Volume 7, Issue 9

2016 September - 16 articles

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Articles (16)

  • Case Report
  • Open Access
8 Citations
6,082 Views
2 Pages

Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia

  • Yun Tae Hwang,
  • Tracy Dudding,
  • Solange Mabel Aliaga,
  • Marta Arpone,
  • David Francis,
  • Xin Li,
  • Howard Robert Slater,
  • Carolyn Rogers,
  • Lesley Bretherton and
  • David Eugeny Godler
  • + 2 authors

21 September 2016

Mosaicism for FMR1 premutation (PM: 55–199 CGG)/full mutation (FM: >200 CGG) alleles or the presence of unmethylated FM (UFM) have been associated with a less severe fragile X syndrome (FXS) phenotype and fragile X associated tremor/ataxia syndrom...

  • Review
  • Open Access
75 Citations
14,814 Views
21 Pages

DNA Polymerase θ: A Unique Multifunctional End-Joining Machine

  • Samuel J. Black,
  • Ekaterina Kashkina,
  • Tatiana Kent and
  • Richard T. Pomerantz

21 September 2016

The gene encoding DNA polymerase θ (Polθ) was discovered over ten years ago as having a role in suppressing genome instability in mammalian cells. Studies have now clearly documented an essential function for this unique A-family polymerase in the do...

  • Review
  • Open Access
15 Citations
7,371 Views
14 Pages

21 September 2016

The Fragile X-related disorders (FXDs) are a group of clinical conditions resulting from the expansion of a CGG/CCG-repeat tract in exon 1 of the Fragile X mental retardation 1 (FMR1) gene. While expansions of the repeat tract predominate, contractio...

  • Article
  • Open Access
12 Citations
7,807 Views
18 Pages

Regulation of BLM Nucleolar Localization

  • Larissa Tangeman,
  • Michael A. McIlhatton,
  • Patrick Grierson,
  • Joanna Groden and
  • Samir Acharya

21 September 2016

Defects in coordinated ribosomal RNA (rRNA) transcription in the nucleolus cause cellular and organismal growth deficiencies. Bloom’s syndrome, an autosomal recessive human disorder caused by mutated recQ-like helicase BLM, presents with growth defec...

  • Article
  • Open Access
26 Citations
10,328 Views
10 Pages

Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients

  • Binghui Zeng,
  • Xue Xiao,
  • Sijie Li,
  • Hui Lu,
  • Jiaxuan Lu,
  • Ling Zhu,
  • Dongsheng Yu and
  • Wei Zhao

19 September 2016

Hypohidrotic ectodermal dysplasia (HED) is characterized by abnormal development of the teeth, hair, and sweat glands. Ectodysplasin A (EDA), Ectodysplasin A receptor (EDAR), and EDAR-associated death domain (EDARADD) are candidate genes for HED, but...

  • Review
  • Open Access
76 Citations
12,979 Views
20 Pages

The Role of ATRX in the Alternative Lengthening of Telomeres (ALT) Phenotype

  • João P. Amorim,
  • Gustavo Santos,
  • João Vinagre and
  • Paula Soares

19 September 2016

Telomeres are responsible for protecting chromosome ends in order to prevent the loss of coding DNA. Their maintenance is required for achieving immortality by neoplastic cells and can occur by upregulation of the telomerase enzyme or through a homol...

  • Review
  • Open Access
69 Citations
16,583 Views
18 Pages

Reappearance from Obscurity: Mammalian Rad52 in Homologous Recombination

  • Kritika Hanamshet,
  • Olga M. Mazina and
  • Alexander V. Mazin

14 September 2016

Homologous recombination (HR) plays an important role in maintaining genomic integrity. It is responsible for repair of the most harmful DNA lesions, DNA double-strand breaks and inter-strand DNA cross-links. HR function is also essential for proper...

  • Review
  • Open Access
70 Citations
11,635 Views
33 Pages

Telomerase Regulation from Beginning to the End

  • Deanna Elise MacNeil,
  • Hélène Jeanne Bensoussan and
  • Chantal Autexier

14 September 2016

The vast body of literature regarding human telomere maintenance is a true testament to the importance of understanding telomere regulation in both normal and diseased states. In this review, our goal was simple: tell the telomerase story from the bi...

  • Review
  • Open Access
103 Citations
12,951 Views
15 Pages

Mechanisms and Physiological Roles of the CBL-CIPK Networking System in Arabidopsis thaliana

  • Jingjing Mao,
  • S. M. Nuruzzaman Manik,
  • Sujuan Shi,
  • Jiangtao Chao,
  • Yirong Jin,
  • Qian Wang and
  • Haobao Liu

8 September 2016

Calcineurin B-like protein (CBL)-CBL-interacting protein kinase (CIPK) network is one of the vital regulatory mechanisms which decode calcium signals triggered by environmental stresses. Although the complicated regulation mechanisms and some novel f...

  • Review
  • Open Access
26 Citations
6,180 Views
13 Pages

Telomerase Activation in Hematological Malignancies

  • Joana Ropio,
  • Jean-Philippe Merlio,
  • Paula Soares and
  • Edith Chevret

7 September 2016

Telomerase expression and telomere maintenance are critical for cell proliferation and survival, and they play important roles in development and cancer, including hematological malignancies. Transcriptional regulation of the rate-limiting subunit of...

  • Review
  • Open Access
123 Citations
15,930 Views
22 Pages

The Telomere/Telomerase System in Chronic Inflammatory Diseases. Cause or Effect?

  • Vasileios Kordinas,
  • Anastasios Ioannidis and
  • Stylianos Chatzipanagiotou

3 September 2016

Telomeres are specialized nucleoprotein structures located at the end of linear chromosomes and telomerase is the enzyme responsible for telomere elongation. Telomerase activity is a key component of many cancer cells responsible for rapid cell divis...

  • Article
  • Open Access
4 Citations
6,385 Views
13 Pages

Towards a Better Molecular Diagnosis of FMR1-Related Disorders—A Multiyear Experience from a Reference Lab

  • Sylwia Olimpia Rzońca,
  • Monika Gos,
  • Daniel Szopa,
  • Danuta Sielska-Rotblum,
  • Aleksandra Landowska,
  • Agnieszka Szpecht-Potocka,
  • Michał Milewski,
  • Jolanta Czekajska,
  • Anna Abramowicz and
  • Jerzy Bal
  • + 3 authors

2 September 2016

The article summarizes over 20 years of experience of a reference lab in fragile X mental retardation 1 gene (FMR1) molecular analysis in the molecular diagnosis of fragile X spectrum disorders. This includes fragile X syndrome (FXS), fragile X-assoc...

  • Review
  • Open Access
169 Citations
20,836 Views
18 Pages

1 September 2016

Telomeres are tandem repeat DNA sequences present at the ends of each eukaryotic chromosome to stabilize the genome structure integrity. Telomere lengths progressively shorten with each cell division. Inflammation and oxidative stress, which are impl...

  • Article
  • Open Access
41 Citations
10,671 Views
12 Pages

Possible Therapeutic Doses of Cannabinoid Type 1 Receptor Antagonist Reverses Key Alterations in Fragile X Syndrome Mouse Model

  • Maria Gomis-González,
  • Arnau Busquets-Garcia,
  • Carlos Matute,
  • Rafael Maldonado,
  • Susana Mato and
  • Andrés Ozaita

31 August 2016

Fragile X syndrome (FXS) is the most common monogenetic cause of intellectual disability. The cognitive deficits in the mouse model for this disorder, the Fragile X Mental Retardation 1 (Fmr1) knockout (KO) mouse, have been restored by different phar...

  • Review
  • Open Access
21 Citations
7,156 Views
17 Pages

DNA Polymerases λ and β: The Double-Edged Swords of DNA Repair

  • Elisa Mentegari,
  • Miroslava Kissova,
  • Laura Bavagnoli,
  • Giovanni Maga and
  • Emmanuele Crespan

31 August 2016

DNA is constantly exposed to both endogenous and exogenous damages. More than 10,000 DNA modifications are induced every day in each cell’s genome. Maintenance of the integrity of the genome is accomplished by several DNA repair systems. The core enz...

  • Review
  • Open Access
74 Citations
22,216 Views
25 Pages

30 August 2016

The Hippo signaling pathway is a highly-conserved developmental pathway that plays an essential role in organ size control, tumor suppression, tissue regeneration and stem cell self-renewal. The YES-associated protein (YAP) and the transcriptional co...

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Genes - ISSN 2073-4425