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M Digweed

Showing results (31-40 of 42) with videos related to

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Nucleic Acids Research|September 26, 1988
Oocyte and somatic 5S ribosomal RNA and 5S RNA encoding genes in Xenopus tropicalisW Nietfeld, M Digweed, H Mentzel, et al.
European Journal of Biochemistry|March 3, 1986
Small cytoplasmic RNAs from human placental free mRNPs. Structure and their effect on in vitro protein synthesisH Lorberboum, M Digweed, V A Erdmann, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Animal Cognition|July 17, 2016
Episodic-like memory in zebrafishTrevor J Hamilton, Allison Myggland, Erika Duperreault, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Localisation of a Fanconi anaemia gene to chromosome 9pK Saar, D Schindler, R D Wegner, et al.
Nature Genetics|February 1, 1994
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)A Reis, H C Hennies, L Langbein, et al.
Nature Genetics|November 7, 1998
The Fanconi anaemia group G gene FANCG is identical with XRCC9J P de Winter, Q Waisfisz, M A Rooimans, et al.
American Journal of Human Genetics|April 17, 1999
The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Nucleic Acids Research|September 26, 1988
Oocyte and somatic 5S ribosomal RNA and 5S RNA encoding genes in Xenopus tropicalisW Nietfeld, M Digweed, H Mentzel, et al.
European Journal of Biochemistry|March 3, 1986
Small cytoplasmic RNAs from human placental free mRNPs. Structure and their effect on in vitro protein synthesisH Lorberboum, M Digweed, V A Erdmann, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Animal Cognition|July 17, 2016
Episodic-like memory in zebrafishTrevor J Hamilton, Allison Myggland, Erika Duperreault, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Localisation of a Fanconi anaemia gene to chromosome 9pK Saar, D Schindler, R D Wegner, et al.
Nature Genetics|February 1, 1994
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)A Reis, H C Hennies, L Langbein, et al.
Nature Genetics|November 7, 1998
The Fanconi anaemia group G gene FANCG is identical with XRCC9J P de Winter, Q Waisfisz, M A Rooimans, et al.
American Journal of Human Genetics|April 17, 1999
The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
Pageof 5