Pages that link to "Q28587383"
Jump to navigation
Jump to search
The following pages link to The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain (Q28587383):
Displaying 42 items.
- Oligophrenin 1 (Q21985183) (← links)
- A BAR domain-mediated autoinhibitory mechanism for RhoGAPs of the GRAF family (Q24309329) (← links)
- A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbα (Q24336512) (← links)
- The human minor histocompatibility antigen 1 is a RhoGAP (Q24337574) (← links)
- Regulation of small GTPases by GEFs, GAPs, and GDIs (Q26825750) (← links)
- Functional cross-talk between ras and rho pathways: a Ras-specific GTPase-activating protein (p120RasGAP) competitively inhibits the RhoGAP activity of deleted in liver cancer (DLC) tumor suppressor by masking the catalytic arginine finger (Q28397100) (← links)
- Reduced gamma oscillations in a mouse model of intellectual disability: a role for impaired repetitive neurotransmission? (Q28538532) (← links)
- Deciphering the Molecular and Functional Basis of RHOGAP Family Proteins: A SYSTEMATIC APPROACH TOWARD SELECTIVE INACTIVATION OF RHO FAMILY PROTEINS. (Q30276221) (← links)
- A novel in-frame deletion affecting the BAR domain of OPHN1 in a family with intellectual disability and hippocampal alterations. (Q30413008) (← links)
- Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain (Q30479819) (← links)
- The BNIP-2 and Cdc42GAP homology (BCH) domain of p50RhoGAP/Cdc42GAP sequesters RhoA from inactivation by the adjacent GTPase-activating protein domain. (Q34123413) (← links)
- Characterization of a novel GTPase-activating protein associated with focal adhesions and the actin cytoskeleton (Q34378405) (← links)
- Control of synapse development and plasticity by Rho GTPase regulatory proteins. (Q35084942) (← links)
- Oligophrenin-1 (OPHN1), a gene involved in X-linked intellectual disability, undergoes RNA editing and alternative splicing during human brain development (Q35123027) (← links)
- Rho proteins, mental retardation and the neurobiological basis of intelligence (Q35974513) (← links)
- Rho-linked genes and neurological disorders (Q36447580) (← links)
- Current knowledge of the large RhoGAP family of proteins (Q36707513) (← links)
- Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement (Q36841531) (← links)
- Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12 (Q37208457) (← links)
- Lack of the presynaptic RhoGAP protein oligophrenin1 leads to cognitive disabilities through dysregulation of the cAMP/PKA signalling pathway. (Q37350712) (← links)
- Inhibition and termination of physiological responses by GTPase activating proteins (Q37980724) (← links)
- Reversing synapse loss in Alzheimer's disease: Rho-guanosine triphosphatases and insights from other brain disorders (Q38318392) (← links)
- Lymphovascular invasion is associated with poor survival in gastric cancer: an application of gene-expression and tissue array techniques (Q38439688) (← links)
- Oligophrenin-1 regulates number, morphology and synaptic properties of adult-born inhibitory interneurons in the olfactory bulb (Q39289677) (← links)
- Drebrins and Connexins: A Biomedical Perspective (Q40060712) (← links)
- Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation (Q42110943) (← links)
- Pharmacological rescue of adult hippocampal neurogenesis in a mouse model of X-linked intellectual disability (Q42317106) (← links)
- Adult neurogenesis in intellectual disabilities (Q42341762) (← links)
- GAP1 family members constitute bifunctional Ras and Rap GTPase-activating proteins (Q42734763) (← links)
- Autoinhibition of p50 Rho GTPase-activating protein (GAP) is released by prenylated small GTPases (Q45185610) (← links)
- Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family (Q45845758) (← links)
- The minor histocompatibility antigen 1 (HMHA1)/ArhGAP45 is a RacGAP and a novel regulator of endothelial integrity (Q47366682) (← links)
- The X-linked mental retardation protein oligophrenin-1 is required for dendritic spine morphogenesis (Q47913103) (← links)
- Oligophrenin-1 Connects Exocytotic Fusion to Compensatory Endocytosis in Neuroendocrine Cells (Q48150013) (← links)
- Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity (Q48386718) (← links)
- Rapid reversal of impaired inhibitory and excitatory transmission but not spine dysgenesis in a mouse model of mental retardation. (Q50778272) (← links)
- Additive lymph node dissection may be necessary in minute submucosal cancer of the stomach after endoscopic resection. (Q51407101) (← links)
- Deletion of the OPHN1 gene detected by aCGH. (Q51894055) (← links)
- Rho GTPases in Intellectual Disability: From Genetics to Therapeutic Opportunities. (Q55644124) (← links)
- The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migration (Q89776436) (← links)
- ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual Disability (Q89881954) (← links)
- BAR domain proteins-a linkage between cellular membranes, signaling pathways, and the actin cytoskeleton (Q93231136) (← links)