The original publication can be found at www.springerlink.comA novel gene has been characterized, designated C16orf5, with an unusually high content of proline residues (40% over 104 residues) at the N-terminus of the protein. The C-terminus of the protein is also cysteine rich with 14 cysteine residues present. Analysis using Northern and dot blots showed that the highest expression of this gene is in the brain. The gene was located on chromosome 16 at band p13.3 by FISH to metaphase chromosomes. Southern blot analysis with a human–rodent somatic cell hybrid panel showed a location between the somatic hybrid breakpoints 23HA and CY196. This gene comprises at least four exons and an open reading frame of 786 bp encoding a predicted protein ...
As a part of our project for accumulating sequence information of the coding regions of unidentified...
Identifying the proteome variation in different parts of the body provides fundamental molecular det...
In our series of human cDNA projects for accumulating sequence information on the coding sequences o...
A novel human gene has been identified by in-depth bioinformatics analysis of chromosome 21 segment ...
This study reports the characterization of a novel human gene, chromosome 3 open reading frame 6 (C3...
We isolated full-length cDNA clones from size-fractionated cDNA libraries of human immature myeloid ...
<div><p>The mammalian brain is a complex organ composed of many specialized cells, harboring sets of...
Here, we report on the sequence features and chromosomal location of a novel human gene which shares...
The mammalian brain is a complex organ composed of many specialized cells, harboring sets of both co...
As a part of our cDNA project for deducing the coding sequence of unidentified human genes, we newly...
As part of an effort to identify genes potentially involved in the Down Syndrome pathogenesis, in th...
The mammalian brain is a complex organ composed of many specialized cells, harboring sets of both co...
We have cloned and characterized a novel gene (C11orf9) mapping to chromosome 11q12→q13.1. The trans...
www.elsevier.com/Macro-array differential hybridization of a collection of 5058 human gene transcrip...
A number of severe neurodegenerative diseases, such as Huntington’s disease (HD), are caused by a si...
As a part of our project for accumulating sequence information of the coding regions of unidentified...
Identifying the proteome variation in different parts of the body provides fundamental molecular det...
In our series of human cDNA projects for accumulating sequence information on the coding sequences o...
A novel human gene has been identified by in-depth bioinformatics analysis of chromosome 21 segment ...
This study reports the characterization of a novel human gene, chromosome 3 open reading frame 6 (C3...
We isolated full-length cDNA clones from size-fractionated cDNA libraries of human immature myeloid ...
<div><p>The mammalian brain is a complex organ composed of many specialized cells, harboring sets of...
Here, we report on the sequence features and chromosomal location of a novel human gene which shares...
The mammalian brain is a complex organ composed of many specialized cells, harboring sets of both co...
As a part of our cDNA project for deducing the coding sequence of unidentified human genes, we newly...
As part of an effort to identify genes potentially involved in the Down Syndrome pathogenesis, in th...
The mammalian brain is a complex organ composed of many specialized cells, harboring sets of both co...
We have cloned and characterized a novel gene (C11orf9) mapping to chromosome 11q12→q13.1. The trans...
www.elsevier.com/Macro-array differential hybridization of a collection of 5058 human gene transcrip...
A number of severe neurodegenerative diseases, such as Huntington’s disease (HD), are caused by a si...
As a part of our project for accumulating sequence information of the coding regions of unidentified...
Identifying the proteome variation in different parts of the body provides fundamental molecular det...
In our series of human cDNA projects for accumulating sequence information on the coding sequences o...