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A global evaluation of mitochondrial DNA diversity and distribution of dromedary, from north-central Saudi Arabia
A global evaluation of mitochondrial DNA diversity and distribution of dromedary, from north-central Saudi Arabia
Knowledge of genetic variability within and among types and breeds of dromedary (Camelus dromedarius L.) can be a valuable...
miR-7160 inhibits gastric cancer cell proliferation and metastasis by silencing
miR-7160 inhibits gastric cancer cell proliferation and metastasis by silencing
Upregulation of homeoprotein SIX1 in gastric cancer (GC) is related to tumour proliferation and invasion. MicroRNA-7160 (m...
A novel missense variant in associated with nonobstructive azoospermia
A novel missense variant in associated with nonobstructive azoospermia
The most severe type of male infertility is nonobstructive azoospermia (NOA), where there is no sperm in the ejaculate due...
Assessment of the contribution of and genes in the pathogenesis of celiac disease
Assessment of the contribution of and genes in the pathogenesis of celiac disease
Vitamin-D deficiency (VDD) is a global health concern. It is known to play a critical role in the immunomodulation, and th...
The complete mitochondrial genome of the deep-sea methanotrophic sponges and : leveraging ‘waste’ in metagenomic data
The complete mitochondrial genome of the deep-sea methanotrophic sponges and : leveraging ‘waste’ in metagenomic data
A significant proportion of next-generation sequencing (NGS) data ends up not being used since they comprise information o...
Development of specific molecular markers for medicinal peony () with double flower
Development of specific molecular markers for medicinal peony () with double flower
In China, medicinal Paeonia lactiflora with double flowers (DFs) does not produce seeds, yet it possesses significantly hi...
Mitochondrial control region sequences show high genetic connectivity in the brownstripe snapper, (Quoy and Gaimard, 1824) from the east coast of Peninsular Malaysia
Mitochondrial control region sequences show high genetic connectivity in the brownstripe snapper, (Quoy and Gaimard, 1824) from the east coast of Peninsular Malaysia
The Brownstripe Snapper, Lutjanus vitta (Quoy and Gaimard, 1824) is a commercially important snapper extensively caught in...
JAG1 overexpression partially rescues muscle function in a zebrafish model of duchenne muscular dystrophy
JAG1 overexpression partially rescues muscle function in a zebrafish model of duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by progressive muscle degeneration and loss o...
YY1 as a mediator to enhance the resistance of KRAS mutant colorectal cancer cells to cetuximab
YY1 as a mediator to enhance the resistance of KRAS mutant colorectal cancer cells to cetuximab
Cetuximab has been indicated as the mainstay of metastatic colorectal cancer (CRC) therapy, of which application was imped...
Maternal effect on the inheritance of pericarp colour and grain dimension in rice ( L.)
Maternal effect on the inheritance of pericarp colour and grain dimension in rice ( L.)
This study aimed to understand the maternal influence on the inheritance of pericarp colour and grain dimensions in rice, ...
Generation of albino C57BL/6J mice by CRISPR embryo editing of the mouse tyrosinase locus
Generation of albino C57BL/6J mice by CRISPR embryo editing of the mouse tyrosinase locus
After the arrival of the CRISPR/Cas9 genome editing technology, genetic engineering of model organisms has become much fas...
Gonadal mosaicism and paradoxical phenotype in encephalopathy: a case report of two siblings
Gonadal mosaicism and paradoxical phenotype in encephalopathy: a case report of two siblings
The neurite extension and migration factor (NEXMIF) encephalopathy is an X-linked disorder that is chara...
Expanding the genetic and phenotypic spectrum of Baker–Gordon syndrome: a new de novo SYT1 variant
Expanding the genetic and phenotypic spectrum of Baker–Gordon syndrome: a new de novo SYT1 variant
We report the case of a Spanish pediatric patient with developmental delay, hypotonia, feeding difficulties, visual proble...
A global evaluation of mitochondrial DNA diversity and distribution of dromedary, Camelus dromedarius from north-central Saudi Arabia
A global evaluation of mitochondrial DNA diversity and distribution of dromedary, Camelus dromedarius from north-central Saudi Arabia
Knowledge of genetic variability within and among types and breeds of dromedary (Camelus dromedarius L.) can be a valuable...
COQ7 splice site variant causing a spastic paraparesis phenotype in siblings
COQ7 splice site variant causing a spastic paraparesis phenotype in siblings
The COQ7 gene is one of the causative genes for primary COQ10 deficiency-related disorders. OMIM-related phenotypes includ...
miR-7160 inhibits gastric cancer cell proliferation and metastasis by silencing SIX1
miR-7160 inhibits gastric cancer cell proliferation and metastasis by silencing SIX1
Upregulation of homeoprotein SIX1 in gastric cancer (GC) is related to tumour proliferation and invasion. MicroRNA-7160 (m...
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia
The most severe type of male infertility is nonobstructive azoospermia (NOA), where there is no sperm in the ejaculate due...
Assessment of the contribution of VDR and VDBP/GC genes in the pathogenesis of celiac disease
Assessment of the contribution of VDR and VDBP/GC genes in the pathogenesis of celiac disease
Vitamin-D deficiency (VDD) is a global health concern. It is known to play a critical role in the immunomodulation, and th...
A novel intron variant in the prolactin gene associated with eggshell weight and thickness with putative alternative splicing patterns in chickens
A novel intron variant in the prolactin gene associated with eggshell weight and thickness with putative alternative splicing patterns in chickens
Raising Iraqi indigenous chickens (IIC) is restricted by their thin and low eggshell weights. Due to the importance of the...
Germline genetic variants in a case of familial cancer: RAD51D and four other co-segregated variants
Germline genetic variants in a case of familial cancer: RAD51D and four other co-segregated variants
Cancer is a multifactorial, multi-step process of pathogenesis; however, in the case of familial cancers, genetic aetiolog...
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein
Intellectual developmental disorder, X-linked 104 (XLID104), caused by the FRMPD4 gene variant, is a rare X-linked genetic...
Genetic characterization and linkage analysis of spotted leaf 6, liguleless and lax panicle traits in mutant rice
Genetic characterization and linkage analysis of spotted leaf 6, liguleless and lax panicle traits in mutant rice
Phenotypic mutants are valuable resources for elucidating the function of genes responsible for their expression. This stu...
The first complete mitochondrial genome of the critically endangered Malaysian giant turtle, Orlitia borneensis (Testudines: Geoemydidae)
The first complete mitochondrial genome of the critically endangered Malaysian giant turtle, Orlitia borneensis (Testudines: Geoemydidae)
We present here the complete mitochondrial sequence of the critically endangered Malaysian giant turtle, Orlitia borneensi...
Mitogenome features and phylogenetic analysis of red algae, Grateloupia cornea (Rhodophyta, Halymeniales)
Mitogenome features and phylogenetic analysis of red algae, Grateloupia cornea (Rhodophyta, Halymeniales)
The mitogenome is an important tool for taxonomic and evolutionary investigation. Here, a few complete mitogenomes of red ...
Extraction of genomic DNA for sequencing from snail Helix lucorum
Extraction of genomic DNA for sequencing from snail Helix lucorum
Genomic studies make it possible to breakthrough in many fields such as biochemistry, physiology, phylogenetics, etc., tho...
Special clinical entity with 15q26 deletion: a novel case report
Special clinical entity with 15q26 deletion: a novel case report
In the past, there were no easily distinct and recognizable features as a guide for precise clinical and genetic diagnosis...
Detection of caudal type homeobox 1 (CDX1) gene methylated DNA, as a stool-based diagnostic biomarker in colorectal cancer
Detection of caudal type homeobox 1 (CDX1) gene methylated DNA, as a stool-based diagnostic biomarker in colorectal cancer
Colorectal cancer (CRC) is known to develop due to the accumulation of both genetic and epigenetic alterations, resulting ...
The effect of modification of DNA interference on myostatin gene expression in mice
The effect of modification of DNA interference on myostatin gene expression in mice
Myostatin is a known negative regulator of muscle tissue growth. Thus, an inhibitor of myostatin may be therapeutically us...
Molecular data reveals a new genus of blindsnakes within Asiatyphlopinae from India
Molecular data reveals a new genus of blindsnakes within Asiatyphlopinae from India
The genus Indotyphlops has a widespread distribution in the Indian landmass and Southeast Asia, with 20 reported species. ...
FSTest: an efficient tool for cross-population fixation index estimation on variant call format files
FSTest: an efficient tool for cross-population fixation index estimation on variant call format files
Fixation index (Fst) statistics provide critical insights into evolutionary processes affecting the structure of genetic v...
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