<div><p>(A) Protein sequence alignment using Clustal W and BoxShade of C9ORF72 isoform 1 and ALFA-1 isoform 1. Overall, these sequences share 26% identify and 59 % similarity. </p> <p>(B) ALFA-1 has two predicted transcripts and the <i>ok3062</i> deletion mutation spans exons 3 and 4 for both transcripts.</p> <p>(B) RT-PCR confirming the complete loss of expression of the <i>alfa-1</i> transcripts. <i>act-3</i> was used as a control.</p></div
<p>(A) location of <i>ju89</i> on <i>C. elegans</i> chromosome I based on genetic map data, (B) Tran...
Complex traits, including common disease-related traits, are affected by many different genes that f...
<p>The top of this figure shows the alignment of C. elegans and C. briggsae sequences for the altern...
<div><p>An expansion of the hexanucleotide GGGGCC repeat in the first intron of <i>C9ORF72</i> gene ...
An expansion of the hexanucleotide GGGGCC repeat in the first intron of C9ORF72 gene was recently li...
For over 30 years, researchers have taken advantage of genetic balancers and forward genetic screens...
Using combined genetic mapping, Illumina sequencing, bioinformatics analyses, and experimental valid...
Background: Essential genes are required for an organism’s viability and their func...
<p>(A) Amino acid alignment of the human and <i>C. elegans</i> Folliculin sequences (accession numbe...
<p>(A) Protein sequence alignment using Clustal omega of F57B10.9 and SPG20. These sequences share 2...
C. elegans is an important model for genetic studies relevant to human biology and disease. We sough...
<div><p>(A) Multiple sequence alignment of C. elegans H3, H3.3, and H3.3-like proteins. The red box ...
Background: Essential genes are critical for the development of all organisms and are associated wit...
An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with...
An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with...
<p>(A) location of <i>ju89</i> on <i>C. elegans</i> chromosome I based on genetic map data, (B) Tran...
Complex traits, including common disease-related traits, are affected by many different genes that f...
<p>The top of this figure shows the alignment of C. elegans and C. briggsae sequences for the altern...
<div><p>An expansion of the hexanucleotide GGGGCC repeat in the first intron of <i>C9ORF72</i> gene ...
An expansion of the hexanucleotide GGGGCC repeat in the first intron of C9ORF72 gene was recently li...
For over 30 years, researchers have taken advantage of genetic balancers and forward genetic screens...
Using combined genetic mapping, Illumina sequencing, bioinformatics analyses, and experimental valid...
Background: Essential genes are required for an organism’s viability and their func...
<p>(A) Amino acid alignment of the human and <i>C. elegans</i> Folliculin sequences (accession numbe...
<p>(A) Protein sequence alignment using Clustal omega of F57B10.9 and SPG20. These sequences share 2...
C. elegans is an important model for genetic studies relevant to human biology and disease. We sough...
<div><p>(A) Multiple sequence alignment of C. elegans H3, H3.3, and H3.3-like proteins. The red box ...
Background: Essential genes are critical for the development of all organisms and are associated wit...
An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with...
An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with...
<p>(A) location of <i>ju89</i> on <i>C. elegans</i> chromosome I based on genetic map data, (B) Tran...
Complex traits, including common disease-related traits, are affected by many different genes that f...
<p>The top of this figure shows the alignment of C. elegans and C. briggsae sequences for the altern...