Pages that link to "Q37375711"
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The following pages link to Dinesh C. Soares (Q37375711):
Displaying 50 items.
- Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH) (Q21134757) (← links)
- The evolution of TEP1, an exceptionally polymorphic immunity gene in Anopheles gambiae (Q21283875) (← links)
- Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations (Q24298949) (← links)
- The intermediate filament protein, vimentin, is a regulator of NOD2 activity (Q24337903) (← links)
- The central portion of factor H (modules 10-15) is compact and contains a structurally deviant CCP module (Q24646284) (← links)
- Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations (Q24648540) (← links)
- Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas (Q24684993) (← links)
- Solution Structure of Factor I-like Modules from Complement C7 Reveals a Pair of Follistatin Domains in Compact Pseudosymmetric Arrangement (Q27655389) (← links)
- The structure of the KlcA and ArdB proteins reveals a novel fold and antirestriction activity against Type I DNA restriction systems in vivo but not in vitro (Q27658634) (← links)
- Solution Structure of CCP Modules 10–12 Illuminates Functional Architecture of the Complement Regulator, Factor H (Q27673696) (← links)
- DISC1 complexes with TRAK1 and Miro1 to modulate anterograde axonal mitochondrial trafficking (Q28299770) (← links)
- DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness (Q28393891) (← links)
- Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target (Q28551203) (← links)
- Functional insights from the structure of the multifunctional C345C domain of C5 of complement (Q30160375) (← links)
- In silico structure-function analysis of pathological variation in the HSD11B2 gene sequence (Q30390640) (← links)
- Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation (Q33487694) (← links)
- Oxovanadium(IV) cyclam and bicyclam complexes: potential CXCR4 receptor antagonists (Q33639946) (← links)
- Condensin II mutation causes T-cell lymphoma through tissue-specific genome instability (Q34679227) (← links)
- A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression (Q35014891) (← links)
- RPGR: Its role in photoreceptor physiology, human disease, and future therapies. (Q36008733) (← links)
- A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins (Q36083129) (← links)
- The mitosis and neurodevelopment proteins NDE1 and NDEL1 form dimers, tetramers, and polymers with a folded back structure in solution. (Q36294846) (← links)
- Opportunities for new therapies based on the natural regulators of complement activation (Q36357802) (← links)
- DISC1 genetics, biology and psychiatric illness (Q36634401) (← links)
- Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability (Q37101233) (← links)
- NDE1 and NDEL1: twin neurodevelopmental proteins with similar 'nature' but different 'nurture'. (Q37208704) (← links)
- Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy (Q37737834) (← links)
- SAF-A Regulates Interphase Chromosome Structure through Oligomerization with Chromatin-Associated RNAs (Q39190884) (← links)
- PKA phosphorylation of NDE1 is DISC1/PDE4 dependent and modulates its interaction with LIS1 and NDEL1 (Q39366533) (← links)
- NDE1 and NDEL1: multimerisation, alternate splicing and DISC1 interaction (Q39919009) (← links)
- Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia (Q40153548) (← links)
- Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. (Q40453402) (← links)
- A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma (Q41066748) (← links)
- PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins (Q41920057) (← links)
- Highly homologous eEF1A1 and eEF1A2 exhibit differential post-translational modification with significant enrichment around localised sites of sequence variation (Q42051422) (← links)
- Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration (Q42362886) (← links)
- HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 (Q42635953) (← links)
- DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan (Q43015032) (← links)
- An interrupted beta-propeller and protein disorder: structural bioinformatics insights into the N-terminus of alsin (Q46235070) (← links)
- Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator Gene (Q46660605) (← links)
- Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish (Q47073229) (← links)
- A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells. (Q47110589) (← links)
- A structural organization for the Disrupted in Schizophrenia 1 protein, identified by high-throughput screening, reveals distinctly folded regions, which are bisected by mental illness-related mutations (Q47788104) (← links)
- Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodeling (Q48183464) (← links)
- HIV-1 Uncoating and Reverse Transcription Require eEF1A Binding to Surface-Exposed Acidic Residues of the Reverse Transcriptase Thumb Domain. (Q52339973) (← links)
- Large-scale modelling as a route to multiple surface comparisons of the CCP module family (Q57936759) (← links)
- ACS Omega 2017: A Year-End Expression of Appreciation for the Fundamental Contributions of Our Reviewers (Q58210815) (← links)
- Atypical femoral fracture in osteoporosis pseudoglioma syndrome associated with two novel compound heterozygous mutations in LRP5 (Q58210827) (← links)
- eEF1A2 and neuronal degeneration (Q58210845) (← links)
- Structure-based Mapping of DAF Active Site Residues That Accelerate the Decay of C3 Convertases (Q58210854) (← links)