X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (39) 39
index medicus (36) 36
male (24) 24
physics (22) 22
mutation (20) 20
female (18) 18
genetics & heredity (18) 18
experiment (16) 16
high energy physics (14) 14
mitochondrial dna (12) 12
hadron-hadron scattering (11) 11
mitochondrial proteins - genetics (11) 11
pediatrics (11) 11
physics of elementary particles and fields (11) 11
biochemistry & molecular biology (10) 10
child (10) 10
physics, particles & fields (10) 10
adolescent (9) 9
adult (9) 9
clinical neurology (9) 9
high energy physics - experiment (9) 9
analysis (8) 8
animals (8) 8
article (8) 8
elementary particles, quantum field theory (8) 8
human genetics (8) 8
infant (8) 8
metabolic diseases (8) 8
mitochondria - metabolism (8) 8
mitochondrial diseases - genetics (8) 8
oxidative phosphorylation (8) 8
quantum field theories, string theory (8) 8
cells, cultured (7) 7
cms (7) 7
genetics (7) 7
infant, newborn (7) 7
medicine & public health (7) 7
molecular sequence data (7) 7
nuclear experiment (7) 7
phenomenology (7) 7
amino acid sequence (6) 6
biochemistry, general (6) 6
child, preschool (6) 6
children (6) 6
deficiency (6) 6
disease (6) 6
dna mutational analysis (6) 6
endocrinology & metabolism (6) 6
enzymes (6) 6
fibroblasts (6) 6
genetic aspects (6) 6
internal medicine (6) 6
magnetic resonance imaging (6) 6
mice (6) 6
mutation - genetics (6) 6
pathology (6) 6
physics - high energy physics - experiment (6) 6
skeletal-muscle (6) 6
biology (5) 5
cell biology (5) 5
cells (5) 5
classical and quantum gravitation, relativity theory (5) 5
dna (5) 5
electron transport complex i - genetics (5) 5
gene expression (5) 5
genomics (5) 5
life sciences (5) 5
middle aged (5) 5
mitochondria (5) 5
mitochondrial diseases - diagnosis (5) 5
mutations (5) 5
original article (5) 5
particle physics (5) 5
quantum physics (5) 5
research (5) 5
base sequence (4) 4
brain - pathology (4) 4
cardiomyopathy (4) 4
complex-i (4) 4
dna, mitochondrial - genetics (4) 4
electron transport complex i - deficiency (4) 4
fatal outcome (4) 4
genes (4) 4
leigh syndrome (4) 4
medicine (4) 4
medicine, research & experimental (4) 4
membrane proteins - genetics (4) 4
metabolism (4) 4
mitochondria - enzymology (4) 4
mitochondrial disease (4) 4
models, molecular (4) 4
phenotype (4) 4
physical sciences (4) 4
physics and astronomy (4) 4
physiological aspects (4) 4
respiratory-chain (4) 4
saccharomyces-cerevisiae (4) 4
0202 atomic, molecular, nuclear, particle and plasma physics (3) 3
0206 quantum physics (3) 3
[phys.hexp]physics [physics]/high energy physics - experiment [hep-ex] (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Neuro-Oncology, ISSN 0167-594X, 6/2018, Volume 138, Issue 2, pp. 391 - 399
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 2014, Volume 95, Issue 3, pp. 315 - 325
Cytochrome c oxidase (COX) deficiency is a frequent biochemical abnormality in mitochondrial disorders, but a large fraction of cases remains genetically... 
CELLS | DISEASES | 2.8 ANGSTROM | QUANTIFICATION | INVOLVEMENT | GENETICS & HEREDITY | BRAIN-STEM | ENCEPHALOMYOPATHY | INHIBITOR | COMPLEX-I DEFICIENCY | CHILDREN
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2014, Volume 95, Issue 3, pp. 315 - 325
Journal Article
by Khachatryan, V and Sirunyan, A.M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Fabjan, C and Friedl, M and Frühwirth, R and Ghete, V.M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Taurok, A and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Suarez Gonzalez, J and Alderweireldt, S and Bansal, M and Bansal, S and Cornelis, T and De Wolf, E.A and Janssen, X and Knutsson, A and Luyckx, S and Ochesanu, S and Roland, C and Roland, G and Roland, B and Rougny, R and Van De Klundert, M and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D'Hondt, J and Daci, N and Heracleous, N and Keaveney, J and Kim, M.S and Kim, V and Kim, T.J and Kim, D.H and Kim, Y and Kim, G.N and Kim, J.H and Kim, H and Kim, J.Y and Lowette, S and Maes, M and Olbrechts, A and Python, Q and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G.P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Dobur, D and Favart, L and Favart, D and Gay, A.P.R and Grebenyuk, A and Léonard, A and Mohammadi, A and Perniè, L and Reis, T and Seva, T and Thomas, S and Thomas, L and Vander Velde, C and Vanlaer, P and Wang, Q and Wang, F and Wang, D and Wang, Z and Wang, J and Wang, R.J and Wang, X and ... and Fermi National Accelerator Lab. (FNAL), Batavia, IL (United States)
Physics Letters B, ISSN 0370-2693, 11/2014, Volume 738, pp. 274 - 293
A search for excited quarks decaying into the final state is presented. The analysis is based on data corresponding to an integrated luminosity of 19.7 fb... 
CMS | Jet | Photon | Physics | photon | jet | PHYSICS OF ELEMENTARY PARTICLES AND FIELDS | physics
Journal Article
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 2015, Volume 38, Issue 3, pp. 391 - 403
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2013, Volume 22, Issue 4, pp. 656 - 667
Journal Article
by Khachatryan, V and Sirunyan, A.M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Friedl, M and Frühwirth, R and Ghete, V.M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Suarez Gonzalez, J and Alderweireldt, S and Bansal, S and Cornelis, T and De Wolf, E.A and Janssen, X and Knutsson, A and Lauwers, J and Luyckx, S and Ochesanu, S and Rougny, R and Van De Klundert, M and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D'Hondt, J and Daci, N and Heracleous, N and Keaveney, J and Lowette, S and Maes, M and Olbrechts, A and Python, Q and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G.P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Dobur, D and Favart, L and Gay, A.P.R and Grebenyuk, A and Léonard, A and Mohammadi, A and Perniè, L and Randle-conde, A and Reis, T and Seva, T and Thomas, L and Vander Velde, C and Vanlaer, P and Wang, J and Zenoni, F and Adler, V and Beernaert, K and Benucci, L and Cimmino, A and Costantini, S and Crucy, S and Dildick, S and Fagot, A and Garcia, G and Mccartin, J and Ocampo Rios, A.A and Ryckbosch, D and Salva Diblen, S and Sigamani, M and Strobbe, N and Thyssen, F and Tytgat, M and Yazgan, E and Zaganidis, N and Basegmez, S and ...
Nature, ISSN 0028-0836, 06/2015, Volume 522, Issue 7554, pp. 68 - 72
A joint measurement is presented of the branching fractions B0s→μ+μ− and B0→μ+μ− in proton-proton collisions at the LHC by the CMS and LHCb experiments. The... 
High Energy Physics - Phenomenology | Physics | High Energy Physics - Experiment
Journal Article
Annals of Neurology, ISSN 0364-5134, 2014, Volume 76, Issue 1, pp. 134 - 139
Hypomyelinating disorders of the central nervous system are still a diagnostic challenge, as many patients remain without genetic diagnosis. Using magnetic... 
Journal Article
Annals of Neurology, ISSN 0364-5134, 2014, Volume 76, pp. 134 - 139
Hypomyelinating disorders of the central nervous system are still a diagnostic challenge, as many patients remain without genetic diagnosis. Using magnetic... 
Journal Article
Scientific Reports, ISSN 2045-2322, 2015, Volume 5, p. 8035
In primary fibroblasts from Leigh Syndrome (LS) patients, isolated mitochondrial complex I deficiency is associated with increased reactive oxygen species... 
Journal Article
by Khachatryan, V and Sirunyan, A M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Fabjan, C and Friedl, M and Frühwirth, R and Ghete, V M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Taurok, A and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Gonzalez, J Suarez and Alderweireldt, S and Bansal, M and Bansal, S and Cornelis, T and De Wolf, E A and Janssen, X and Knutsson, A and Luyckx, S and Ochesanu, S and Roland, B and Rougny, R and Van De Klundert, M and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D’Hondt, J and Daci, N and Heracleous, N and Keaveney, J and Lowette, S and Maes, M and Olbrechts, A and Python, Q and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Dobur, D and Favart, L and Gay, A P. R and Grebenyuk, A and Léonard, A and Mohammadi, A and Perniè, L and Reis, T and Seva, T and Thomas, L and Velde, C Vander and Vanlaer, P and Wang, J and Adler, V and Beernaert, K and Benucci, L and Cimmino, A and Costantini, S and Crucy, S and Dildick, S and Fagot, A and Garcia, G and Mccartin, J and Rios, A A. Ocampo and Ryckbosch, D and Diblen, S Salva and Sigamani, M and Strobbe, N and Thyssen, F and Tytgat, M and Yazgan, E and Zaganidis, N and ... and CMS Collaboration and The CMS collaboration and Fermi National Accelerator Lab. (FNAL), Batavia, IL (United States)
Journal of High Energy Physics, ISSN 1126-6708, 9/2014, Volume 2014, Issue 9, pp. 1 - 64
Journal Article