Fabian Glaser
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ConSurf 2005: the projection of evolutionary conservation scores of residues on protein structures
M Landau, I Mayrose, Y Rosenberg, F Glaser, E Martz, T Pupko, ...
Nucleic acids research 33 (suppl_2), W299-W302, 2005
ConSurf: identification of functional regions in proteins by surface-mapping of phylogenetic information
F Glaser, T Pupko, I Paz, RE Bell, D Bechor-Shental, E Martz, N Ben-Tal
Bioinformatics 19 (1), 163-164, 2003
Comparative genome sequence analysis underscores mycoparasitism as the ancestral life style of Trichoderma
CP Kubicek, A Herrera-Estrella, V Seidl-Seiboth, DA Martinez, ...
Genome biology 12, 1-15, 2011
Rate4Site: an algorithmic tool for the identification of functional regions in proteins by surface mapping of evolutionary determinants within their homologues
T Pupko, RE Bell, I Mayrose, F Glaser, N Ben-Tal
Bioinformatics 18 (suppl_1), S71-S77, 2002
Diverse Lifestyles and Strategies of Plant Pathogenesis Encoded in the Genomes of Eighteen Dothideomycetes Fungi
RA Ohm, N Feau, B Henrissat, CL Schoch, BA Horwitz, KW Barry, ...
PLoS pathogens 8 (12), e1003037, 2012
ConSurf: using evolutionary data to raise testable hypotheses about protein function
G Celniker, G Nimrod, H Ashkenazy, F Glaser, E Martz, I Mayrose, ...
Israel Journal of Chemistry 53 (3‐4), 199-206, 2013
ConSeq: the identification of functionally and structurally important residues in protein sequences
C Berezin, F Glaser, J Rosenberg, I Paz, T Pupko, P Fariselli, R Casadio, ...
Bioinformatics 20 (8), 1322-1324, 2004
Residue frequencies and pairing preferences at protein–protein interfaces
F Glaser, DM Steinberg, IA Vakser, N Ben‐Tal
Proteins: Structure, Function, and Bioinformatics 43 (2), 89-102, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell’s waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
S Melchionda, N Ahituv, L Bisceglia, T Sobe, F Glaser, R Rabionet, ...
The American Journal of Human Genetics 69 (3), 635-640, 2001
A method for localizing ligand binding pockets in protein structures
F Glaser, RJ Morris, RJ Najmanovich, RA Laskowski, JM Thornton
PROTEINS: Structure, Function, and Bioinformatics 62 (2), 479-488, 2006
Photosystem I gene cassettes are present in marine virus genomes
I Sharon, A Alperovitch, F Rohwer, M Haynes, F Glaser, ...
Nature 461 (7261), 258-262, 2009
Ferritin is secreted via 2 distinct nonclassical vesicular pathways
M Truman-Rosentsvit, D Berenbaum, L Spektor, LA Cohen, ...
Blood, The Journal of the American Society of Hematology 131 (3), 342-352, 2018
Expansion of signal transduction pathways in fungi by extensive genome duplication
LM Corrochano, A Kuo, M Marcet-Houben, S Polaino, A Salamov, ...
Current Biology 26 (12), 1577-1584, 2016
The ConSurf‐HSSP database: the mapping of evolutionary conservation among homologs onto PDB structures
F Glaser, Y Rosenberg, A Kessel, T Pupko, N Ben‐Tal
PROTEINS: Structure, Function, and Bioinformatics 58 (3), 610-617, 2005
Comparative metagenomics of microbial traits within oceanic viral communities
I Sharon, N Battchikova, EM Aro, C Giglione, T Meinnel, F Glaser, ...
The ISME journal 5 (7), 1178-1190, 2011
A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency
I Lasry, YA Seo, H Ityel, N Shalva, B Pode-Shakked, F Glaser, B Berman, ...
Journal of Biological Chemistry 287 (35), 29348-29361, 2012
Microbial rhodopsins on leaf surfaces of terrestrial plants
N Atamna‐Ismaeel, OM Finkel, F Glaser, I Sharon, R Schneider, AF Post, ...
Environmental microbiology 14 (1), 140-146, 2012
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein
I Gottfried, M Landau, F Glaser, WL Di, J Ophir, B Mevorah, N Ben-Tal, ...
Human molecular genetics 11 (11), 1311-1316, 2002
Bacterial anoxygenic photosynthesis on plant leaf surfaces
N Atamna‐Ismaeel, O Finkel, F Glaser, C von Mering, JA Vorholt, ...
Environmental microbiology reports 4 (2), 209-216, 2012
A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function
I Lasry, B Berman, R Straussberg, Y Sofer, H Bessler, M Sharkia, F Glaser, ...
Blood, The Journal of the American Society of Hematology 112 (5), 2055-2061, 2008
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