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    <title>Julien, J-P.</title>
    <link>http://repub.eur.nl/res/aut/2234/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Sequence and structure of the mouse gene coding for the largest neurofilament subunit. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2437/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>We have determined the complete nucleotide sequence of the mouse gene encoding the neurofilament NF-H protein. The C-terminal domain of NF-H is very rich in charged amino acids (aa) and contains a 3-aa sequence, Lys-Ser-Pro, that is repeated 51 times within a stretch of 368 aa. The location of this serine-rich repeat in the phosphorylated domain of NF-H indicates that it represents the major protein kinase recognition site. The nfh gene shares two common intron positions with the nfl and nfm genes, but has an additional intron that occurs at a location equivalent to one of the introns in non-neuronal intermediate filament-coding genes. This additional nfh intron may have been acquired via duplication of a primordial intermediate filament gene.</description>
    </item> <item>
      <title>The structure of a human neurofilament gene (NF-L): A unique exon-intron organization in the intermediate filament gene family. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2408/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description>We have cloned and determined the nucleotide sequence of the human gene for the neurofilament subunit NF-L. The cloned DNA contains the entire transcriptional unit and generates two mRNAs of approx. 2.6 and 4.3 kb after transfection into mouse L-cells. The NF-L gene has an unexpected intron-exon organization in that it entirely lacks introns at positions found in other members of the intermediate filament gene family. It contains only three introns that do not define protein domains. We discuss possible evolutionary schemes that could explain these results.</description>
    </item> <item>
      <title>The human neurofilament gene (NEFL) is located on the short arm of chromosome 8. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2414/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description>We have localized the gene coding for the human neurofilament light chain (NEFL) to chromosome band 8p2.1 by Southern blotting of DNA from hybrid cell panels and in situ hybridization to metaphase chromosomes.</description>
    </item> <item>
      <title>Cloning and developmental expression of the murine neurofilament gene family. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2397/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>DNA clones encoding the 3 mouse neurofilament (NF) genes have been isolated by cross-hybridization with a previously described NF-L cDNA probe from the rat. Screening of a lambda gt10 cDNA library prepared from mouse brain RNA led to the cloning of an NF-L cDNA of 2.0 kb that spans the entire coding region of 541 amino acids and of an NF-M cDNA that covers 219 amino acids from the internal alpha-helical region and the carboxy-terminal domains of the protein. These cDNA clones were used as probes to screen mouse genomic libraries, and cosmid clones containing both NF-L and NF-M sequences were isolated as well as overlapping cosmids containing the NF-H gene. This strongly suggests that the 3 neurofilament genes are organised in a cluster and derived by gene duplication of a common ancestral gene. RNA blot analyses using specific DNA probes for each of the genes indicate that NF mRNAs are differentially expressed during brain development. The NF-L and NF-M mRNAs are detected early in the embryonal brain, with a progressive increase in their levels during development, while the NF-H mRNA is barely detectable at embryonal stages and accumulates later in the postnatal brain.</description>
    </item> <item>
      <title>Specific detection of neuronal cell bodies: in situ hybridization with a biotin-labelled neurofilament cDNA probe. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2399/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>We have used a biotinylated, 300-nucleotide cDNA probe which encodes the 68,000 MW neurofilament protein to detect neurofilament-specific mRNA in situ. The neurofilament message specifically demonstrates the neuronal cell bodies, in contrast to the usual antibody staining which detects their neurites. The hybridization is detected only in neuronal structures. Consequently, detection of the biotinylated neurofilament DNA probe by silver-intensified streptavidin-gold can be specifically used to identify neuronal cell bodies.</description>
    </item> <item>
      <title>Cloning of a cDNA encoding the smallest neurofilament protein from the rat (Article)</title>
      <link>http://repub.eur.nl/res/pub/2389/</link>
      <pubDate>1985-01-01T00:00:00Z</pubDate>
      <description>We have cloned a cDNA coding for the smallest rat neurofilament protein. The cDNA is 861 nucleotides long coding for 287 amino acids from the internal alpha-helical region and the carboxy-terminal tail domain of the neurofilament protein. Comparison of the porcine, mouse and rat neurofilament protein sequences shows that the protein is highly conserved (greater than 93% identity). Blot analysis indicates that the cDNA is derived from a single neurofilament gene that codes for two different poly(A)+ mRNA species.</description>
    </item>
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