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E Hellsten

Showing results (11-20 of 19) with videos related to

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Developmental Biology|January 11, 2002
Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5bE Hellsten, J P Evans, D J Bernard, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A single PCR marker in strong allelic association with the infantile form of neuronal ceroid lipofuscinosis facilitates reliable prenatal diagnostics and disease carrier identificationJ Vesa, E Hellsten, T P Mäkelä, et al.
Oncogene|December 21, 1995
The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger proteinT P Mäkelä, E Hellsten, J Vesa, et al.
Genomics|November 1, 1995
Visual mapping by fiber-FISHM Heiskanen, E Hellsten, O P Kallioniemi, et al.
Genomics|June 1, 1993
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysisE Hellsten, J Vesa, M C Speer, et al.
Nature|August 17, 1995
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosisJ Vesa, E Hellsten, L A Verkruyse, et al.
American Journal of Human Genetics|October 1, 1993
Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypesR Williams, J Vesa, I Järvelä, et al.
Genomics|January 20, 1995
Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locusE Hellsten, J Vesa, M Heiskanen, et al.
Human Molecular Genetics|February 1, 1994
Assignment of sterol carrier protein X/sterol carrier protein 2 to 1p32 and its exclusion as the causative gene for infantile neuronal ceroid lipofuscinosisJ Vesa, E Hellsten, B L Barnoski, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Developmental Biology|January 11, 2002
Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5bE Hellsten, J P Evans, D J Bernard, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A single PCR marker in strong allelic association with the infantile form of neuronal ceroid lipofuscinosis facilitates reliable prenatal diagnostics and disease carrier identificationJ Vesa, E Hellsten, T P Mäkelä, et al.
Oncogene|December 21, 1995
The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger proteinT P Mäkelä, E Hellsten, J Vesa, et al.
Genomics|November 1, 1995
Visual mapping by fiber-FISHM Heiskanen, E Hellsten, O P Kallioniemi, et al.
Genomics|June 1, 1993
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysisE Hellsten, J Vesa, M C Speer, et al.
Nature|August 17, 1995
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosisJ Vesa, E Hellsten, L A Verkruyse, et al.
American Journal of Human Genetics|October 1, 1993
Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypesR Williams, J Vesa, I Järvelä, et al.
Genomics|January 20, 1995
Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locusE Hellsten, J Vesa, M Heiskanen, et al.
Human Molecular Genetics|February 1, 1994
Assignment of sterol carrier protein X/sterol carrier protein 2 to 1p32 and its exclusion as the causative gene for infantile neuronal ceroid lipofuscinosisJ Vesa, E Hellsten, B L Barnoski, et al.
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