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C Aslanidis

Showing results (31-40 of 44) with videos related to

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European Journal of Biochemistry|December 1, 1996
Isolation and characterization of a 14.5-kDa trichloroacetic-acid-soluble translational inhibitor protein from human monocytes that is upregulated upon cellular differentiationG Schmiedeknecht, C Kerkhoff, E Orsó, et al.
Klinische Padiatrie|March 18, 2014
Neonatal respiratory insufficiency caused by an (homozygous) ABCA3-stop mutation: a systematic evaluation of therapeutic optionsJ Winter, S Essmann, A Kidszun, et al.
Nucleic Acids Research|May 25, 1992
A two-dimensional YAC pooling strategy for library screening via STS and Alu-PCR methodsC T Amemiya, M J Alegria-Hartman, C Aslanidis, et al.
Clinical Genetics|March 3, 2009
Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 geneC Suriu, M Khayat, M Weiler, et al.
Nature|February 6, 1992
Cloning of the essential myotonic dystrophy region and mapping of the putative defectC Aslanidis, G Jansen, C Amemiya, et al.
Genomics|July 1, 1992
Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene regionG Shutler, R G Korneluk, C Tsilfidis, et al.
Journal of Lipid Research|May 1, 1999
Transcription factors Sp1 and AP-2 mediate induction of acid sphingomyelinase during monocytic differentiationT Langmann, C Buechler, S Ries, et al.
Nature|February 6, 1992
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyJ Buxton, P Shelbourne, J Davies, et al.
Biochimica Et Biophysica Acta|July 31, 2001
Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndromeK Lapicka-Bodzioch, M Bodzioch, M Krüll, et al.
BMJ Case Reports|June 19, 2012
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonateHussain Parappil, Ahmad Al Baridi, Sajjad ur Rahman, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
European Journal of Biochemistry|December 1, 1996
Isolation and characterization of a 14.5-kDa trichloroacetic-acid-soluble translational inhibitor protein from human monocytes that is upregulated upon cellular differentiationG Schmiedeknecht, C Kerkhoff, E Orsó, et al.
Klinische Padiatrie|March 18, 2014
Neonatal respiratory insufficiency caused by an (homozygous) ABCA3-stop mutation: a systematic evaluation of therapeutic optionsJ Winter, S Essmann, A Kidszun, et al.
Nucleic Acids Research|May 25, 1992
A two-dimensional YAC pooling strategy for library screening via STS and Alu-PCR methodsC T Amemiya, M J Alegria-Hartman, C Aslanidis, et al.
Clinical Genetics|March 3, 2009
Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 geneC Suriu, M Khayat, M Weiler, et al.
Nature|February 6, 1992
Cloning of the essential myotonic dystrophy region and mapping of the putative defectC Aslanidis, G Jansen, C Amemiya, et al.
Genomics|July 1, 1992
Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene regionG Shutler, R G Korneluk, C Tsilfidis, et al.
Journal of Lipid Research|May 1, 1999
Transcription factors Sp1 and AP-2 mediate induction of acid sphingomyelinase during monocytic differentiationT Langmann, C Buechler, S Ries, et al.
Nature|February 6, 1992
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyJ Buxton, P Shelbourne, J Davies, et al.
Biochimica Et Biophysica Acta|July 31, 2001
Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndromeK Lapicka-Bodzioch, M Bodzioch, M Krüll, et al.
BMJ Case Reports|June 19, 2012
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonateHussain Parappil, Ahmad Al Baridi, Sajjad ur Rahman, et al.
Pageof 5