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INF2 and ROBO2 gene mutation in an Indian family with end stage renal ...
A cryptic splicing mutation in the INF2 gene causing Charcot‐Marie ...
A very rare case report with INF2 gene mutation related sporadic FSGS ...
Mutations in the formin gene INF2 cause focal segmental ...
INF2 Gene Focal Segmental Glomerulosclerosis Type 5 Genetic Test Cost ...
(PDF) Mutations in the formin gene INF2 cause focal segmental ...
(PDF) Mutations in the INF2 gene account for a significant proportion ...
INF2 Gene - GeneCards | INF2 Protein | INF2 Antibody
(PDF) INF2 p.Arg214Cys mutation in a Chinese family with rapidly ...
INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic Test ...
Mutations in the INF2 gene account for a significant proportion of ...
(PDF) Variable renal phenotype in a family with an INF2 mutation
Pedigree of a family with the INF2 p.Arg214Cys mutation (I2, II3 ...
Effect of R246Q mutation on podocyte related gene transcription. (a ...
FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in ...
INF2 mutations cause kidney disease through a gain-of-function ...
| Model for how CMT mutations in INF2 reduce mitochondrial mobility ...
The formin INF2 in disease: progress from 10 years of research ...
The Inverted Formin INF2 Sorts It Out: Developmental Cell
INF2 structure and location of mutations in familial FSGS and ...
A complex containing lysine-acetylated actin inhibits the formin INF2 ...
Schematic of the proposed model of INF2 function on microtubule ...
Pathogenic mutations of the INF2 DID-encoding exons. The exons encoding ...
Locations of variants in the INF2 domain structure. The distribution of ...
Mice with mutant Inf2 show impaired podocyte and slit diaphragm ...
INF2 Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy | NEJM
Spectrum of INF2 mutations and associated phenotypes among familial and ...
INF2 mutations in patients with a broad... : Journal of the Peripheral ...
INF2 - Wikipedia
(PDF) INF2 formin variants linked to human inherited kidney disease ...
(PDF) Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal ...
(PDF) De novo INF2 mutations expand the genetic spectrum of hereditary ...
Predicted structural changes caused by pathogenic INF2 mutations in the ...
(facing page). Effects of Disease-Causing INF2 Mutations on the ...
CaM binds the N-terminal α-helix of INF2. A Schematic of the INF2 ...
Prostate cancer-associated SPOP mutants cannot bind to and promote INF2 ...
Figure 1 from De novo INF2 mutations expand the genetic spectrum of ...
Clinical and genetic data of the nine families with INF2 mutations ...
INF2 domains and DAD interaction with DID or actin monomers. A , bar ...
INF2 depletion causes dispersal of the Golgi apparatus in U2OS cells ...
(PDF) INF2 Mutations in Charcot-Marie-Tooth Disease with Glomerulopathy
Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal ...
Pedigrees with INF2 mutations showing dual CMT and FSGS or single FSGS ...
IQGAP1 interacts directly with INF2. (A) Co-immunoprecipitation of INF2 ...
| Clinical phenotype of eight families with FSGS and mutations in INF2 ...
In silico prediction of the INF2 DID structure, and localization of ...
The Formin INF2 Regulates Basolateral-to-Apical Transcytosis and Lumen ...
The N-terminal extension of INF2 contains two α-helices. A INF2 has an ...
INF2 expression in zebrafish. a. Sequencing alignment of INF2 protein ...
The N terminus of INF2 does not display a high-affinity direct ...
Model for how CMT mutations in INF2 reduce mitochondrial mobility ...
INF2 splice variants. (A) Domain architecture of INF2. C-Terminal ...
INF2 does not localize to ER in U2OS cells. (A) U2OS cells transfected ...
Clinical and Pathological Heterogeneity in FSGS due to INF2 Mutations ...
| Scope of INF2 mutations in familial FSGS | Download Table
INF2 formin variants linked to human inherited kidney disease reprogram ...
Effect of disease-causing INF2 mutations on mDia interaction. (A) The ...
Spectrum of the INF2 mutations identified so far and clinical ...
INF2 knockdown blocks the exit of MAL vesicles from perinuclear ...
Domains, regulation and function of the diaphanous-related formin INF2 ...
(PDF) INF2 Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy.pdf
Characterization of INF2 as a MAL-interacting protein and analysis of ...
Purified INF2 full-length is constitutively active. (a) Schematic ...
New inverted formin 2 (INF2) mutations in familial focal and segmental ...
The structure, regulation, and function of INF2. A Structure and ...
INF2, actin polymerization and FSGS - Renal Fellow Network
Altered Endoplasmic Reticulum Integrity and Organelle Interactions in ...
Sequence alterations in members (I2, II3, III5) of families. Sequencing ...
Inverted formins: A subfamily of atypical formins - Hegsted - 2017 ...
A novel mutation, outside of the candidate region for diagnosis, in the ...
Formins in Human Disease
Hotspots for inverted formin 2 (INF2) variants in FSGS, CMT, and aHUS ...
INF2_DID interferes in the mDia2-mediated Rho/F-actin/ SRF pathway ...
Immunohistochemisty (IHC), Prognostic value, and Genetic mutations of ...
Regulation of INF2-mediated actin polymerization through site-specific ...
Schematic overview depicting so far identified players in genetic forms ...
Clinical, Electrophysiological, and Genetic Characteristics of Patients ...
Schematic representation of the proposed mechanism for development of ...
Constructs and western blot of INF2. (A) Constructs used in this study ...
INF2-Mediated Severing through Actin Filament Encirclement and ...
Constitutive activity of purified INF2, and inhibition by a brain ...
Pedigree diagrams of selected families from our cohorts of patients ...
Figure 2 from A 16-year-old patient with Charcot Marie Tooth disease in ...
