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K Marek

Showing results (91-100 of 112) with videos related to

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Archivum Immunologiae Et Therapiae Experimentalis|March 25, 1998
Culture of human nasal epithelial cells from nasal polyps on collagen matrixM L Kowalski, R Pawliczak, J Woźniak, et al.
Medycyna Pracy|January 1, 1995
[Examination of health effects from exposure to metallic mercury in workers employed in production of chlorine and aldehyde. II. Assessment of kidney lesions]K Marek, T Wocka-Marek, M Zajac-Nedza, et al.
The Journal of Prevention of Alzheimer'S Disease|November 6, 2019
Randomized, Placebo Controlled Trial of NPT088, A Phage-Derived, Amyloid-Targeted Treatment for Alzheimer's DiseaseD Michelson, M Grundman, K Magnuson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001
Genetic remodeling of protein glycosylation in vivo induces autoimmune diseaseD Chui, G Sellakumar, R Green, et al.
Journal of the American Medical Informatics Association : JAMIA|July 22, 1998
Challenges and issues related to implementation of nursing vocabularies in computer-based systemsP Button, I Androwich, L Hibben, et al.
Genes and Immunity|July 11, 2014
Identification of functional, short-lived isoform of linker for activation of T cells (LAT)M Kłossowicz, K Marek-Bukowiec, M M Arbulo-Echevarria, et al.
Arztliche Jugendkunde|January 1, 1987
[Physical development of infants and small children--a longitudinal study]G J Bewer, R Barluschke, A Baudisch, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 23, 1998
Iodine-123-beta-CIT and iodine-123-FPCIT SPECT measurement of dopamine transporters in healthy subjects and Parkinson's patientsJ P Seibyl, K Marek, K Sheff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2006
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutationWilliam C Nichols, Diane K Marek, Michael W Pauciulo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2006
Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's diseaseNathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Archivum Immunologiae Et Therapiae Experimentalis|March 25, 1998
Culture of human nasal epithelial cells from nasal polyps on collagen matrixM L Kowalski, R Pawliczak, J Woźniak, et al.
Medycyna Pracy|January 1, 1995
[Examination of health effects from exposure to metallic mercury in workers employed in production of chlorine and aldehyde. II. Assessment of kidney lesions]K Marek, T Wocka-Marek, M Zajac-Nedza, et al.
The Journal of Prevention of Alzheimer'S Disease|November 6, 2019
Randomized, Placebo Controlled Trial of NPT088, A Phage-Derived, Amyloid-Targeted Treatment for Alzheimer's DiseaseD Michelson, M Grundman, K Magnuson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001
Genetic remodeling of protein glycosylation in vivo induces autoimmune diseaseD Chui, G Sellakumar, R Green, et al.
Journal of the American Medical Informatics Association : JAMIA|July 22, 1998
Challenges and issues related to implementation of nursing vocabularies in computer-based systemsP Button, I Androwich, L Hibben, et al.
Genes and Immunity|July 11, 2014
Identification of functional, short-lived isoform of linker for activation of T cells (LAT)M Kłossowicz, K Marek-Bukowiec, M M Arbulo-Echevarria, et al.
Arztliche Jugendkunde|January 1, 1987
[Physical development of infants and small children--a longitudinal study]G J Bewer, R Barluschke, A Baudisch, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 23, 1998
Iodine-123-beta-CIT and iodine-123-FPCIT SPECT measurement of dopamine transporters in healthy subjects and Parkinson's patientsJ P Seibyl, K Marek, K Sheff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2006
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutationWilliam C Nichols, Diane K Marek, Michael W Pauciulo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2006
Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's diseaseNathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Pageof 12