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I Mononen

Showing results (31-40 of 63) with videos related to

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Clinical Chemistry|November 4, 1998
Molecular diagnosis of Finnish type infantile neuronal ceroid lipofuscinosis by restriction fragment length polymorphism and oligonucleotide ligation assayE L Romppanen, P Valtonen, T Mononen, et al.
Scandinavian Journal of Haematology|March 1, 1985
Adaptation of the May-Grünwald-Giemsa staining method for automated differential counting of blood leukocytes by a Hematrak analyzerI M Penttilä, E Mahlamäki, I Mononen, et al.
FEBS Letters|July 21, 1997
Recombinant human glycosylasparaginase catalyzes hydrolysis of L-asparagineT Noronkoski, I B Stoineva, D D Petkov, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 1, 1993
Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradationI Mononen, K J Fisher, V Kaartinen, et al.
The Journal of Biological Chemistry|February 17, 1995
Localization of the disulfide bond involved in post-translational processing of glycosylasparaginase and disrupted by a mutation in the Finnish-type aspartylglycosaminuriaA L McCormack, I Mononen, V Kaartinen, et al.
Cancer Genetics and Cytogenetics|November 1, 1994
Multiple karyotypic abnormalities in three cases of small cell variant of T-cell prolymphocytic leukemiaK Heinonen, E Mahlamäki, E Hämäläinen, et al.
Clinical Chemistry|March 1, 1994
Enzymatic diagnosis of aspartylglycosaminuria by fluorometric assay of glycosylasparaginase in serum, plasma, or lymphocytesI Mononen, T Mononen, P Ylikangas, et al.
Human Genetics|January 1, 1992
Chromosomal localization of the human glycoasparaginase gene to 4q32-q33C Morris, N Heisterkamp, J Groffen, et al.
The American Journal of Pathology|October 20, 1998
Progressive neurodegeneration in aspartylglycosaminuria miceI Gonzalez-Gomez, I Mononen, N Heisterkamp, et al.
Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Clinical Chemistry|November 4, 1998
Molecular diagnosis of Finnish type infantile neuronal ceroid lipofuscinosis by restriction fragment length polymorphism and oligonucleotide ligation assayE L Romppanen, P Valtonen, T Mononen, et al.
Scandinavian Journal of Haematology|March 1, 1985
Adaptation of the May-Grünwald-Giemsa staining method for automated differential counting of blood leukocytes by a Hematrak analyzerI M Penttilä, E Mahlamäki, I Mononen, et al.
FEBS Letters|July 21, 1997
Recombinant human glycosylasparaginase catalyzes hydrolysis of L-asparagineT Noronkoski, I B Stoineva, D D Petkov, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 1, 1993
Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradationI Mononen, K J Fisher, V Kaartinen, et al.
The Journal of Biological Chemistry|February 17, 1995
Localization of the disulfide bond involved in post-translational processing of glycosylasparaginase and disrupted by a mutation in the Finnish-type aspartylglycosaminuriaA L McCormack, I Mononen, V Kaartinen, et al.
Cancer Genetics and Cytogenetics|November 1, 1994
Multiple karyotypic abnormalities in three cases of small cell variant of T-cell prolymphocytic leukemiaK Heinonen, E Mahlamäki, E Hämäläinen, et al.
Clinical Chemistry|March 1, 1994
Enzymatic diagnosis of aspartylglycosaminuria by fluorometric assay of glycosylasparaginase in serum, plasma, or lymphocytesI Mononen, T Mononen, P Ylikangas, et al.
Human Genetics|January 1, 1992
Chromosomal localization of the human glycoasparaginase gene to 4q32-q33C Morris, N Heisterkamp, J Groffen, et al.
The American Journal of Pathology|October 20, 1998
Progressive neurodegeneration in aspartylglycosaminuria miceI Gonzalez-Gomez, I Mononen, N Heisterkamp, et al.
Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
Pageof 7