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Molecular Genetics and Metabolism
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June 5, 1999
Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene
J M Hartikainen, W Ju, K E Wisniewski, et al.
Physical Review Letters
|
February 27, 2016
Observation of Wakefield Suppression in a Photonic-Band-Gap Accelerator Structure
Evgenya I Simakov, Sergey A Arsenyev, Cynthia E Buechler, et al.
Human Genetics
|
March 7, 1998
Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene
N Zhong, K E Wisniewski, A L Kaczmarski, et al.
Chest
|
April 20, 1999
Efficacy of salmeterol xinafoate in the treatment of COPD
D A Mahler, J F Donohue, R A Barbee, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individuals
E C Jenkins, E A Devine-Gage, X L Yao, et al.
Scientific Reports
|
February 24, 2023
Fabrication of THz corrugated wakefield structure and its high power test
H Kong, M Chung, D S Doran, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 21, 2025
Intraputaminal Delivery of Adeno-Associated Virus Serotype 2-Glial Cell Line-Derived Neurotrophic Factor in Mild or Moderate Parkinson's Disease
Amber D Van Laar, Chadwick W Christine, Nicolás Phielipp, et al.
Annals of Neurology
|
February 5, 1998
Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis
K E Wisniewski, N Zhong, W Kaczmarski, et al.
Physical Review Letters
|
February 15, 2020
Single Shot Characterization of High Transformer Ratio Wakefields in Nonlinear Plasma Acceleration
R Roussel, G Andonian, W Lynn, et al.
Physical Review Letters
|
March 25, 2017
Precision Control of the Electron Longitudinal Bunch Shape Using an Emittance-Exchange Beam Line
G Ha, M H Cho, W Namkung, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Molecular Genetics and Metabolism
|
June 5, 1999
Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene
J M Hartikainen, W Ju, K E Wisniewski, et al.
Physical Review Letters
|
February 27, 2016
Observation of Wakefield Suppression in a Photonic-Band-Gap Accelerator Structure
Evgenya I Simakov, Sergey A Arsenyev, Cynthia E Buechler, et al.
Human Genetics
|
March 7, 1998
Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene
N Zhong, K E Wisniewski, A L Kaczmarski, et al.
Chest
|
April 20, 1999
Efficacy of salmeterol xinafoate in the treatment of COPD
D A Mahler, J F Donohue, R A Barbee, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individuals
E C Jenkins, E A Devine-Gage, X L Yao, et al.
Scientific Reports
|
February 24, 2023
Fabrication of THz corrugated wakefield structure and its high power test
H Kong, M Chung, D S Doran, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 21, 2025
Intraputaminal Delivery of Adeno-Associated Virus Serotype 2-Glial Cell Line-Derived Neurotrophic Factor in Mild or Moderate Parkinson's Disease
Amber D Van Laar, Chadwick W Christine, Nicolás Phielipp, et al.
Annals of Neurology
|
February 5, 1998
Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis
K E Wisniewski, N Zhong, W Kaczmarski, et al.
Physical Review Letters
|
February 15, 2020
Single Shot Characterization of High Transformer Ratio Wakefields in Nonlinear Plasma Acceleration
R Roussel, G Andonian, W Lynn, et al.
Physical Review Letters
|
March 25, 2017
Precision Control of the Electron Longitudinal Bunch Shape Using an Emittance-Exchange Beam Line
G Ha, M H Cho, W Namkung, et al.
Page
of 14