about
TOPDB: topology data bank of transmembrane proteinsDiscrete molecular dynamics can predict helical prestructured motifs in disordered proteinsDual coding in alternative reading frames correlates with intrinsic protein disorder.High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.Narcolepsy patients have antibodies that stain distinct cell populations in rat brain and influence sleep patterns.DisProt 7.0: a major update of the database of disordered proteins.Whole-Body Barometric Plethysmography Characterizes Upper Airway Obstruction in 3 Brachycephalic Breeds of Dogs.The other side of the coin: functional and structural versatility of ADF/cofilins.The role of structural disorder in cell cycle regulation, related clinical proteomics, disease development and drug targeting.Intrinsically disordered proteins: emerging interaction specialists.Outcomes and prognostic factors of surgical treatments for brachycephalic obstructive airway syndrome in 3 breeds.HAEdb: a novel interactive, locus-specific mutation database for the C1 inhibitor gene.Conformational risk factors of brachycephalic obstructive airway syndrome (BOAS) in pugs, French bulldogs, and bulldogs.Characterization of ABL exon 7 deletion by molecular genetic and bioinformatic methods reveals no association with imatinib resistance in chronic myeloid leukemia.Differential adaptation of REM sleep latency, intermediate stage and theta power effects of escitalopram after chronic treatment.Endotracheal tube placement during computed tomography of brachycephalic dogs alters upper airway dimensional measurements.Acute escitalopram treatment inhibits REM sleep rebound and activation of MCH-expressing neurons in the lateral hypothalamus after long term selective REM sleep deprivation.Chronic escitalopram treatment caused dissociative adaptation in serotonin (5-HT) 2C receptor antagonist-induced effects in REM sleep, wake and theta wave activity.Structural determinants governing S100A4-induced isoform-selective disassembly of nonmuscle myosin II filaments.Analysis of the population heterogeneity in Hungary using fifteen forensically informative STR markers.Asymmetric PCR increases efficiency of melting peak analysis on the LightCycler.Brachycephalic obstructive airway syndromeDisProt 7.0: a major update of the database of disordered proteinsAn overlooked DNA source for non-invasive genetic analysis in birds[A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across EuropeAssociation of celiac disease and hereditary angioneurotic edemaFrequencies of two common mutations (c.35delG and c.167delT) of the connexin 26 gene in different populations of HungaryLong-range interactions in nonsense-mediated mRNA decay are mediated by intrinsically disordered protein regionsCharacterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lajos Kalmár
@ast
Lajos Kalmár
@en
Lajos Kalmár
@es
Lajos Kalmár
@nl
Lajos Kalmár
@sl
type
label
Lajos Kalmár
@ast
Lajos Kalmár
@en
Lajos Kalmár
@es
Lajos Kalmár
@nl
Lajos Kalmár
@sl
prefLabel
Lajos Kalmár
@ast
Lajos Kalmár
@en
Lajos Kalmár
@es
Lajos Kalmár
@nl
Lajos Kalmár
@sl
P106
P31
P496
0000-0003-3691-8350