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Human Molecular Genetics
|
September 15, 1999
A novel deficiency of mitochondrial ATPase of nuclear origin
J Houstek, P Klement, D Floryk, et al.
Bratislavske Lekarske Listy
|
January 7, 2005
Maternal hyperphenylalaninemias in healthy Czech population of pregnant women: 30 years experience with screening, prevention and treatment
J Hyanek, L Kozak, E Hrabincova, et al.
Inorganic Chemistry
|
January 22, 2020
An Application Exploiting Aurophilic Bonding and iClick to Produce White Light Emitting Materials
Christopher C Beto, Charles J Zeman, Yajing Yang, et al.
Neuromuscular Disorders : NMD
|
October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic origin
W Sperl, P Jesina, J Zeman, et al.
Nano Letters
|
December 28, 2022
Direct Observation of the Pressure-Induced Structural Variation in Gold Nanoclusters and the Correlated Optical Response
Qi Li, Charles J Zeman, Bora Kalkan, et al.
Clinical Genetics
|
September 29, 2009
SURF1 missense mutations promote a mild Leigh phenotype
D Piekutowska-Abramczuk, M Magner, E Popowska, et al.
ACS Nano
|
July 6, 2026
The Role of Defect Geometry in Localized Emission from Monolayer Tungsten Dichalcogenides
S Carin Gavin, Moumita Kar, Jianguo Wen, et al.
Clinical Genetics
|
July 23, 2016
Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic
K Stehlíková, D Skálová, J Zídková, et al.
Clinical Genetics
|
November 25, 2016
Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II
L Dvorakova, H Vlaskova, A Sarajlija, et al.
Journal of the American Chemical Society
|
February 7, 2022
Direct Observation of Modulated Radical Spin States in Metal-Organic Frameworks by Controlled Flexibility
Xiaofeng Chen, Haomiao Xie, Emmaline R Lorenzo, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 311) with videos related to
Sort By:
Page
of 32
Human Molecular Genetics
|
September 15, 1999
A novel deficiency of mitochondrial ATPase of nuclear origin
J Houstek, P Klement, D Floryk, et al.
Bratislavske Lekarske Listy
|
January 7, 2005
Maternal hyperphenylalaninemias in healthy Czech population of pregnant women: 30 years experience with screening, prevention and treatment
J Hyanek, L Kozak, E Hrabincova, et al.
Inorganic Chemistry
|
January 22, 2020
An Application Exploiting Aurophilic Bonding and iClick to Produce White Light Emitting Materials
Christopher C Beto, Charles J Zeman, Yajing Yang, et al.
Neuromuscular Disorders : NMD
|
October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic origin
W Sperl, P Jesina, J Zeman, et al.
Nano Letters
|
December 28, 2022
Direct Observation of the Pressure-Induced Structural Variation in Gold Nanoclusters and the Correlated Optical Response
Qi Li, Charles J Zeman, Bora Kalkan, et al.
Clinical Genetics
|
September 29, 2009
SURF1 missense mutations promote a mild Leigh phenotype
D Piekutowska-Abramczuk, M Magner, E Popowska, et al.
ACS Nano
|
July 6, 2026
The Role of Defect Geometry in Localized Emission from Monolayer Tungsten Dichalcogenides
S Carin Gavin, Moumita Kar, Jianguo Wen, et al.
Clinical Genetics
|
July 23, 2016
Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic
K Stehlíková, D Skálová, J Zídková, et al.
Clinical Genetics
|
November 25, 2016
Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II
L Dvorakova, H Vlaskova, A Sarajlija, et al.
Journal of the American Chemical Society
|
February 7, 2022
Direct Observation of Modulated Radical Spin States in Metal-Organic Frameworks by Controlled Flexibility
Xiaofeng Chen, Haomiao Xie, Emmaline R Lorenzo, et al.
Page
of 32