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Unprecedented Chain-Length-Dependent Conformational Conversion Between 11/9 and 18/16 Helix in α/β-Hybrid Peptides.
- Published in:
- Angewandte Chemie, 2014, v. 126, n. 48, p. 13347, doi. 10.1002/ange.201407329
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- Publication type:
- Article
Cost-effectiveness analysis of aprepitant in the prevention of chemotherapy-induced nausea and vomiting in Belgium.
- Published in:
- 2008
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- Publication type:
- journal article
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28–29.
- Published in:
- Human Genetics, 2003, v. 112, n. 1, p. 24, doi. 10.1007/s00439-002-0836-x
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- Publication type:
- Article
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
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- Human Genetics, 2002, v. 111, n. 1, p. 26, doi. 10.1007/s00439-002-0736-0
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- Publication type:
- Article
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24–25.
- Published in:
- Human Genetics, 2002, v. 110, n. 4, p. 348, doi. 10.1007/s00439-002-0690-x
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- Publication type:
- Article
Examining Resident Power Building in a Place-Based Initiative.
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- Health Promotion Practice, 2022, v. 23, n. 6, p. 955, doi. 10.1177/15248399211045355
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- Publication type:
- Article
A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
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- International Journal of Dermatology, 2019, v. 58, n. 12, p. 1439, doi. 10.1111/ijd.14452
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- Publication type:
- Article
Synthesis and Structural Characterization of 2:1 [α/Aza]-oligomers.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 34, p. 7643, doi. 10.1002/ejoc.201402628
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- Publication type:
- Article
Robust Helix Formation in a New Family of Oligoureas Based on a Constrained Bicyclic Building Block.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 45, p. 11267, doi. 10.1002/anie.201205842
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- Publication type:
- Article
Consequences of Isostructural Main-Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host-Defense Peptides Based on a Heterogeneous Amide/Urea Backbone.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 2, p. 333, doi. 10.1002/anie.200905591
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- Publication type:
- Article
Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery.
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- FEBS Letters, 2017, v. 591, n. 15, p. 2299, doi. 10.1002/1873-3468.12729
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- Publication type:
- Article
Hearing Is Normal without Connexin30.
- Published in:
- Journal of Neuroscience, 2013, v. 33, n. 2, p. 430, doi. 10.1523/JNEUROSCI.4240-12.2013
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- Publication type:
- Article
Probing the Functional Equivalence of Otoferlin and Synaptotagmin 1 in Exocytosis.
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- Journal of Neuroscience, 2011, v. 31, n. 13, p. 4886, doi. 10.1523/JNEUROSCI.5122-10.2011
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- Publication type:
- Article
Control of Exocytosis by Synaptotagmins and Otoferlin in Auditory Hair Cells.
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- Journal of Neuroscience, 2010, v. 30, n. 40, p. 13281, doi. 10.1523/JNEUROSCI.2528-10.2010
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- Publication type:
- Article
Otoferlin Is Critical for a Highly Sensitive and Linear Calcium-Dependent Exocytosis at Vestibular Hair Cell Ribbon Synapses.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 34, p. 10474, doi. 10.1523/JNEUROSCI.1009-09.2009
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- Publication type:
- Article
Calcium- and Otoferlin-Dependent Exocytosis by Immature Outer Hair Cells.
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- Journal of Neuroscience, 2008, v. 28, n. 8, p. 1798, doi. 10.1523/JNEUROSCI.4653-07.2008
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- Publication type:
- Article
Phylogenetic analysis of Harmonin homology domains.
- Published in:
- BMC Bioinformatics, 2021, v. 22, p. 1, doi. 10.1186/s12859-021-04116-5
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- Publication type:
- Article
Mixed Oligoureas Based on Constrained Bicyclic and Acyclic β-Amino Acids Derivatives: On the Significance of the Subunit Configuration for Folding.
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- Chemistry - A European Journal, 2013, v. 19, n. 50, p. 16963, doi. 10.1002/chem.201302829
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- Publication type:
- Article
Genetics of auditory mechano-electrical transduction.
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- Pflügers Archiv: European Journal of Physiology, 2015, v. 467, n. 1, p. 49, doi. 10.1007/s00424-014-1552-9
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- Publication type:
- Article
Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells.
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- Pflügers Archiv: European Journal of Physiology, 2009, v. 459, n. 1, p. 115, doi. 10.1007/s00424-009-0711-x
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- Publication type:
- Article
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.
- Published in:
- Human Heredity, 2020, v. 85, n. 1, p. 35, doi. 10.1159/000512712
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- Publication type:
- Article
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.
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- Human Heredity, 2019, v. 84, n. 3, p. 109, doi. 10.1159/000503450
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- Publication type:
- Article
Specific Aspects of Consanguinity: Some Examples from the Tunisian Population.
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- Human Heredity, 2014, v. 77, n. 1-4, p. 167, doi. 10.1159/000362167
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- Publication type:
- Article
Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites.
- Published in:
- Journal of Cell Biology, 2003, v. 163, n. 3, p. 559, doi. 10.1083/jcb.200302157
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- Publication type:
- Article
The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3773, doi. 10.1093/hmg/ddt228
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- Publication type:
- Article
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 17, p. 3835, doi. 10.1093/hmg/dds212
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- Publication type:
- Article
Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids.
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- Human Molecular Genetics, 2010, v. 19, n. 18, p. 3557, doi. 10.1093/hmg/ddq271
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- Publication type:
- Article
Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 262, doi. 10.1093/hmg/ddp490
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- Publication type:
- Article
Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4615, doi. 10.1093/hmg/ddp429
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- Publication type:
- Article
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 24, p. 3921, doi. 10.1093/hmg/ddi416
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- Publication type:
- Article
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 3, p. 401, doi. 10.1093/hmg/ddi036
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- Publication type:
- Article
Interactions in the network of Usher syndrome type 1 proteins.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 3, p. 347, doi. 10.1093/hmg/ddi031
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- Publication type:
- Article
Impact of C<sup>α</sup>-Chirality on Supramolecular Self-Assembly in Cyclo-2:1-[α/aza]-Hexamers (D/L-Phe-azaPhe-Ala)<sub>2</sub>.
- Published in:
- European Journal of Organic Chemistry, 2017, v. 2017, n. 32, p. 4703, doi. 10.1002/ejoc.201700555
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- Publication type:
- Article
Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness.
- Published in:
- Frontiers in Behavioral Neuroscience, 2020, v. 14, p. N.PAG, doi. 10.3389/fnbeh.2020.588834
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- Publication type:
- Article
Vasculitis neuropathy mimicking lower limb mono-radiculopathy: a study and follow-up of 8 cases.
- Published in:
- Internal & Emergency Medicine, 2013, v. 8, n. 7, p. 601, doi. 10.1007/s11739-012-0858-x
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- Publication type:
- Article
Parametric PET Imaging of 5HT<sub>2A</sub> Receptor Distribution with <sup>18</sup>F-Setoperone in the Normal Human Neocortex.
- Published in:
- Journal of Nuclear Medicine, 1999, v. 40, n. 1, p. 25
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- Publication type:
- Article
Comparative Quantitation of Cerebral Blood Volume: SPECT Versus PET.
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- Journal of Nuclear Medicine, 1997, v. 38, n. 6, p. 919
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- Publication type:
- Article
Estimation of Neocortical Serotonin-2 Receptor Binding Potential by Single-Dose Fluorine-18-Setoperone Kinetic PET Data Analysis.
- Published in:
- Journal of Nuclear Medicine, 1996, v. 37, n. 1, p. 95
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- Publication type:
- Article
Chronic Mild Hyperhomocysteinemia Induces Aortic Endothelial Dysfunction but Does Not Elevate Arterial Pressure in Rats.
- Published in:
- Journal of Vascular Research, 2005, v. 42, n. 2, p. 148, doi. 10.1159/000083972
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- Publication type:
- Article
Persistence of the Nitric Oxide Pathway in the Aorta of Hypercholesterolemic Apolipoprotein-E-Deficient Mice.
- Published in:
- Journal of Vascular Research, 2003, v. 40, n. 2, p. 87, doi. 10.1159/000070705
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- Publication type:
- Article
Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 19, p. 10352, doi. 10.3390/ijms221910352
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- Publication type:
- Article
Horseradish Peroxidase Immobilized Electrode for Phenothiazine Analysis.
- Published in:
- Electroanalysis, 1998, v. 10, n. 18, p. 1241, doi. 10.1002/(SICI)1521-4109(199812)10:18<1241::AID-ELAN1241>3.0.CO;2-Q
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- Publication type:
- Article
The third-dimensional structure of the complex between an Fv antibody fragment and an analogue of the main immunogenic region of the acetylcholine receptor: A combined two-dimensional NMR, homology, and molecular modeling approach.
- Published in:
- Biopolymers, 2000, v. 53, n. 2, p. 113, doi. 10.1002/(SICI)1097-0282(200002)53:2<113::AID-BIP1>3.0.CO;2-J
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- Publication type:
- Article
Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.
- Published in:
- 2008
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- Publication type:
- Letter
Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation.
- Published in:
- Genes, 2019, v. 10, n. 12, p. 1015, doi. 10.3390/genes10121015
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- Publication type:
- Article
Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy.
- Published in:
- Genes, 2019, v. 10, n. 12, p. 956, doi. 10.3390/genes10120956
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- Publication type:
- Article
The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.
- Published in:
- EMBO Molecular Medicine, 2014, v. 6, n. 7, p. 984, doi. 10.15252/emmm.201403976
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- Publication type:
- Article
Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 1, p. 122, doi. 10.1038/ejhg.2008.155
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- Publication type:
- Article
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 4, p. 279, doi. 10.1038/sj.ejhg.5201147
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- Publication type:
- Article
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 816, doi. 10.1038/sj.ejhg.5201045
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- Publication type:
- Article