Stanley Froehner

Q: What Schools Are Affiliated With Stanley Froehner

Stanley Froehner is affiliated with the following schools: University of Oslo, University of California, Berkeley, University of Sydney, University of Oxford, California Institute of Technology, Stanford University, University of Washington, University of North Carolina at Chapel Hill

Stanley Froehner's AcademicInfluence.com Rankings

Stanley Froehner

Physics

#7976

World Rank

#10067

Historical Rank

#1863

USA Rank

Biophysics

#353

World Rank

#365

Historical Rank

#60

USA Rank

physics Degrees

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Physics

Stanley Froehner's Degrees

PhD Biophysics Stanford University
Masters Physics University of California, Berkeley
Bachelors Physics University of California, Berkeley

Why Is Stanley Froehner Influential?

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According to Wikipedia, Stanley C. Froehner is an American physiologist and biophysicist currently the UW Medicine Distinguished Professor at University of Washington and an Elected Fellow of the American Association for the Advancement of Science.

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Stanley Froehner's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Interaction of Nitric Oxide Synthase with the Postsynaptic Density Protein PSD-95 and α1-Syntrophin Mediated by PDZ Domains (1996) (1641)
An α-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain (2003) (483)
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein (2001) (443)
Interaction of Muscle and Brain Sodium Channels with Multiple Members of the Syntrophin Family of Dystrophin-Associated Proteins (1998) (348)
Delayed K+ clearance associated with aquaporin-4 mislocalization: Phenotypic defects in brains of α-syntrophin-null mice (2003) (341)
Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. (2016) (300)
rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice (2006) (298)
Differential Association of Syntrophin Pairs with the Dystrophin Complex (1997) (245)
The postsynaptic 43k protein clusters muscle nicotinic acetylcholine receptors in xenopus oocytes (1990) (243)
Alpha syntrophin deletion removes the perivascular but not the endothelial pool of aquaporin‐4 at the blood‐brain barrier and delays the development of brain edema in an experimental model of acute hyponatremia (2004) (242)
Absence of α-Syntrophin Leads to Structurally Aberrant Neuromuscular Synapses Deficient in Utrophin (2000) (231)
Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution (1993) (218)
Protein Trafficking and Anchoring Complexes Revealed by Proteomic Analysis of Inward Rectifier Potassium Channel (Kir2.x)-associated Proteins* (2004) (217)
Assembly of the Dystrophin-Associated Protein Complex Does Not Require the Dystrophin Cooh-Terminal Domain (2000) (215)
The Potassium Channel Kir4.1 Associates with the Dystrophin-Glycoprotein Complex via α-Syntrophin in Glia* (2004) (181)
Regulation of ion channel distribution at synapses. (1993) (176)
The submembrane machinery for nicotinic acetylcholine receptor clustering (1991) (176)
In vivo requirement of the α-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4 (2001) (174)
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy (1996) (173)
Isoform Diversity of Dystrobrevin, the Murine 87-kDa Postsynaptic Protein (*) (1996) (167)
Association of utrophin and multiple dystrophin short forms with the mammalian M(r) 58,000 dystrophin-associated protein (syntrophin). (1994) (166)
Skeletal Muscle NADPH Oxidase Is Increased and Triggers Stretch-Induced Damage in the mdx Mouse (2010) (160)
Ultrastructural localization of the Mr 43,000 protein and the acetylcholine receptor in Torpedo postsynaptic membranes using monoclonal antibodies (1984) (160)
Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy (2010) (159)
Golgi and sarcolemmal neuronal NOS differentially regulate contraction-induced fatigue and vasoconstriction in exercising mouse skeletal muscle. (2010) (144)
Differential Membrane Localization and Intermolecular Associations of α-Dystrobrevin Isoforms in Skeletal Muscle (1998) (139)
Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle (1991) (138)
Vasomodulation by Skeletal Muscle–Derived Nitric Oxide Requires &agr;-Syntrophin–Mediated Sarcolemmal Localization of Neuronal Nitric Oxide Synthase (2003) (136)
beta 2-Syntrophin: localization at the neuromuscular junction in skeletal muscle. (1994) (136)
Sildenafil reduces respiratory muscle weakness and fibrosis in the mdx mouse model of Duchenne muscular dystrophy (2012) (134)
A postsynaptic Mr 58,000 (58K) protein concentrated at acetylcholine receptor-rich sites in Torpedo electroplaques and skeletal muscle (1987) (133)
Immunofluorescence localization at the mammalian neuromuscular junction of the Mr 43,000 protein of Torpedo postsynaptic membranes. (1981) (133)
Dephosphorylation of β2‐syntrophin and Ca2+/μ‐calpain‐mediated cleavage of ICA512 upon stimulation of insulin secretion (2001) (116)
beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations. (1997) (113)
The blood—nerve barrier is rich in glucose transporter (1988) (108)
Purification and Properties of Neurospora crassa Laccase (1974) (103)
Monoclonal antibodies to cytoplasmic domains of the acetylcholine receptor. (1983) (98)
A PDZ-containing Scaffold Related to the Dystrophin Complex at the Basolateral Membrane of Epithelial Cells (1999) (96)
Association of the postsynaptic 43K protein with newly formed acetylcholine receptor clusters in cultured muscle cells (1985) (96)
Restoration of 125I-alpha-bungarotoxin binding activity to the alpha subunit of Torpedo acetylcholine receptor isolated by gel electrophoresis in sodium dodecyl sulfate. (1981) (96)
The postsynaptic submembrane machinery at the neuromuscular junction: Requirement for rapsyn and the utrophin/dystrophin-associated complex (2003) (95)
Syntrophins and Dystrobrevins: Defining the Dystrophin Scaffold at Synapses (2002) (92)
Mouse α1- and β2-Syntrophin Gene Structure, Chromosome Localization, and Homology with a Discs Large Domain (*) (1995) (91)
The perivascular pool of aquaporin-4 mediates the effect of osmotherapy in postischemic cerebral edema* (2008) (87)
Signals mediating ion channel clustering at the neuromuscular junction (1998) (86)
Functional Deficits in nNOSμ-Deficient Skeletal Muscle: Myopathy in nNOS Knockout Mice (2008) (86)
Peripheral proteins of postsynaptic membranes from Torpedo electric organ identified with monoclonal antibodies (1984) (85)
Comparison of the subunits of Torpedo californica acetylcholine receptor by peptide mapping. (1979) (84)
Association of the Mr 58,000 postsynaptic protein of electric tissue with Torpedo dystrophin and the Mr 87,000 postsynaptic protein. (1992) (84)
Induction of Neurospora crassa Laccase with Protein Synthesis Inhibitors (1974) (84)
A new therapeutic effect of simvastatin revealed by functional improvement in muscular dystrophy (2015) (83)
Cyclic Peptides as Non-carboxyl-terminal Ligands of Syntrophin PDZ Domains* (1998) (81)
Monoclonal antibody identifies a 200-kDa subunit of the dihydropyridine-sensitive calcium channel. (1987) (79)
Characterization and localization of the Mr = 43,000 proteins associated with acetylcholine receptor-rich membranes. (1983) (78)
Localization of the α 1 and α 2 subunits of the dihydropyridine receptor and ankyrin in skeletal muscle triads (1990) (76)
The role of the postsynaptic cytoskeleton in AChR organization (1986) (76)
Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy. (2008) (74)
Subunit structure of the acetylcholine receptor from denervated rat skeletal muscle. (1977) (73)
The relationship of the postsynaptic 43K protein to acetylcholine receptors in receptor clusters isolated from cultured rat myotubes (1987) (73)
Evidence for direct interaction of Gs alpha with the Ca2+ channel of skeletal muscle. (1991) (71)
Structure of the split PH domain and distinct lipid‐binding properties of the PH–PDZ supramodule of α‐syntrophin (2005) (70)
Nicotinic postsynaptic membranes from Torpedo: sidedness, permeability to macromolecules, and topography of major polypeptides (1982) (69)
Proteomic Analysis Reveals New Cardiac-Specific Dystrophin-Associated Proteins (2012) (69)
Truncated dystrophins can influence neuromuscular synapse structure (2009) (68)
A study of the enzymic transfer of aminoacyl-RNA to Escherichia coli ribosomes. (1968) (66)
Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking alpha- and beta1-syntrophins. (2004) (62)
Structural Abnormalities at Neuromuscular Synapses Lacking Multiple Syntrophin Isoforms (2004) (61)
Biglycan regulates the expression and sarcolemmal localization of dystrobrevin, syntrophin, and nNOS (2006) (61)
Identification of exposed and buried determinants of the membrane-bound acetylcholine receptor from Torpedo californica. (1981) (61)
Dystrophin-associated proteins and synapse formation: Is α-dystroglycan the agrin receptor? (1994) (60)
The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of β2-syntrophin and nNOS in pancreatic β-cells (2000) (58)
Differential effect of α-syntrophin knockout on aquaporin-4 and Kir4.1 expression in retinal macroglial cells in mice (2006) (56)
Multiple calcium channel transcripts in rat osteosarcoma cells: selective activation of alpha 1D isoform by parathyroid hormone. (1995) (55)
Immunochemical demonstration that amino acids 360-377 of the acetylcholine receptor gamma-subunit are cytoplasmic (1985) (53)
α-Syntrophin regulates ARMS localization at the neuromuscular junction and enhances EphA4 signaling in an ARMS-dependent manner (2005) (53)
rAAV6‐Microdystrophin Rescues Aberrant Golgi Complex Organization in mdx Skeletal Muscles (2007) (51)
The α 1 and α 2 polypeptides of the dihydropyridine-sensitive calcium channel differ in developmental expression and tissue distribution (1989) (49)
Interaction of the 43K protein with components of Torpedo postsynaptic membranes. (1985) (46)
Deletion of aquaporin‐4 changes the perivascular glial protein scaffold without disrupting the brain endothelial barrier (2012) (46)
Affinity alkylation labels two subunits of the reduced acetylcholine receptor from mammalian muscle. (1977) (44)
Clustering of the acetylcholine receptor by the 43-kD protein: involvement of the zinc finger domain (1993) (42)
Syntrophins: modular adapter proteins at the neuromuscular junction and the sarcolemma. (1997) (42)
To muster a cluster: anchoring neurotransmitter receptors at synapses. (1998) (41)
β2-Syntrophin Is a Cdk5 Substrate That Restrains the Motility of Insulin Secretory Granules (2010) (40)
Monoclonal antibody to the alpha 1-subunit of the dihydropyridine-binding complex inhibits calcium currents in BC3H1 myocytes. (1988) (39)
Na+–K+–2Cl− Cotransport Inhibitor Attenuates Cerebral Edema Following Experimental Stroke via the Perivascular Pool of Aquaporin-4 (2010) (35)
γ-Syntrophin scaffolding is spatially and functionally distinct from that of the α/β syntrophins (2006) (35)
The Syntrophin-Dystrobrevin Subcomplex in Human Neuromuscular Disorders (2005) (34)
Derepression of tyrosinase synthesis in Neurospora by amino acid analogs. (1970) (34)
Ascites tumor ribonucleic acid polymerases. Isolation, purification, and factor stimulation. (1973) (34)
The α-Syntrophin PH and PDZ Domains Scaffold Acetylcholine Receptors, Utrophin, and Neuronal Nitric Oxide Synthase at the Neuromuscular Junction (2010) (33)
Deficiency of the syntrophins and α-dystrobrevin in patients with inherited myopathy (2003) (32)
Degradation of acetylcholine receptors in muscle cells: effect of leupeptin on turnover rate, intracellular pool sizes, and receptor properties (1983) (32)
Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice. (2015) (31)
Golgi Complex Organization in Skeletal Muscle: A Role for Golgi‐Mediated Glycosylation in Muscular Dystrophies? (2007) (31)
The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of beta2-syntrophin and nNOS in pancreatic beta-cells. (2000) (30)
Sarcolemmal targeting of nNOSμ improves contractile function of mdx muscle. (2016) (29)
DAMAGE, a Novel α-Dystrobrevin-associated MAGE Protein in Dystrophin Complexes* (2004) (29)
Expression of RNA transcripts for the postsynaptic 43 kDa protein in innervated and denervated rat skeletal muscle (1989) (29)
gamma-Syntrophin scaffolding is spatially and functionally distinct from that of the alpha/beta syntrophins. (2006) (28)
Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16–17 (2018) (28)
An anti-peptide antibody specific for the class A calcium channel alpha 1 subunit labels mammalian neuromuscular junction. (1994) (28)
Evaluation of the therapeutic utility of phosphodiesterase 5A inhibition in the mdx mouse model of duchenne muscular dystrophy. (2011) (27)
α-Syntrophin Modulates Myogenin Expression in Differentiating Myoblasts (2010) (27)
Validation of ultrasonography for non‐invasive assessment of diaphragm function in muscular dystrophy (2016) (27)
Differential targeting of nNOS and AQP4 to dystrophin-deficient sarcolemma by membrane-directed α-dystrobrevin (2008) (25)
Faculty Opinions recommendation of Phospholipase Cgamma1 controls surface expression of TRPC3 through an intermolecular PH domain. (2005) (24)
Lack of Sex-Linked Differences in Cerebral Edema and Aquaporin-4 Expression after Experimental Stroke (2008) (24)
Nicotinic Acetylcholine Receptor Stability at the NMJ Deficient in α-Syntrophin In Vivo (2011) (23)
Clusters of 43-kDa protein are absent from genetic variants of C2 muscle cells with reduced acetylcholine receptor expression. (1989) (22)
Properties of the glycoprotein laccase immobilized by two methods. (1975) (21)
The ABCA1 cholesterol transporter associates with one of two distinct dystrophin‐based scaffolds in Schwann cells (2008) (21)
Simvastatin provides long‐term improvement of left ventricular function and prevents cardiac fibrosis in muscular dystrophy (2019) (21)
Functional properties of acetylcholine receptors coexpressed with the 43K protein in heterologous cell systems. (1992) (20)
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. (2000) (19)
Dystrophin-associated protein scaffolding in brain requires α-dystrobrevin (2010) (17)
New insights into the molecular structure of the dihydropyridine-sensitive calcium channel (1988) (16)
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy. (2003) (16)
Localization of the alpha 1 and alpha 2 subunits of the dihydropyridine receptor and ankyrin in skeletal muscle triads. (1990) (16)
Neuregulin-increased expression of acetylcholine receptor epsilon-subunit gene requires ErbB interaction with Shc. (1999) (15)
Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channels (2016) (14)
Lipid abnormalities in alpha/beta2-syntrophin null mice are independent from ABCA1. (2015) (14)
DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes. (2004) (13)
α-Syntrophin is required for the hepatocyte growth factor-induced migration of cultured myoblasts. (2011) (11)
The Light Chains of Microtubule-Associated Proteins MAP1A and MAP1B Interact with α1-Syntrophin in the Central and Peripheral Nervous System (2012) (11)
The alpha 1 and alpha 2 polypeptides of the dihydropyridine-sensitive calcium channel differ in developmental expression and tissue distribution. (1989) (10)
Just say NO to muscle degeneration? (2002) (9)
Simvastatin offers new prospects for the treatment of Duchenne muscular dystrophy (2016) (9)
Regional registration of [6‐14C]glucose metabolism during brain activation of α‐syntrophin knockout mice (2013) (9)
Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1. (2009) (9)
GABARAP and GABAA Receptor Clustering (2002) (9)
PerleCan fix your muscle AChEs (2003) (8)
Anchoring glycine receptors (1993) (8)
Targeted deletion of β1‐syntrophin causes a loss of Kir4.1 from Müller cell endfeet in mouse retina (2019) (7)
Orchestrating aquaporin-4 and connexin-43 expression in brain: Differential roles of α1- and β1-syntrophin. (2021) (7)
β-Dystrobrevin, a New Member of the Dystrophin Family (1997) (7)
Dystrophin-associated proteins and synapse formation: is alpha-dystroglycan the agrin receptor? (1994) (6)
GABARAP and GABA(A) receptor clustering. (2002) (6)
Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophin (2021) (6)
Synapses take the rap (1995) (5)
Evaluation of the specificity of four commercially available antibodies to alpha-syntrophin. (2015) (5)
Functional specialization of retinal Müller cell endfeet depends on an interplay between two syntrophin isoforms (2020) (5)
Adiponectin receptor 1 C-terminus interacts with PDZ-domain proteins such as syntrophins. (2013) (5)
Gathering Glycine Receptors at Synapses (1998) (5)
Mice lacking &agr;‐, &bgr;1‐ and &bgr;2‐syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle (2018) (4)
Ultrastructural Localization of the M r 43,000 Protein and the Acetylcholine Receptor in Torpedo Postsynaptic Membranes Using Monoclonal Antibodies RAPID COMMUNICATIONS (2002) (3)
Rebuttal to: Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy, Verhaart et al. 2020. (2021) (3)
Complete deletion of all alpha-dystrobrevin isoforms does not reveal new neuromuscular junction phenotype. (2007) (3)
Dystrophin-Associated Proteins and Synapse Formation: Is a-Dystroglycan the Agrin Receptor? Minireview (1994) (2)
Systemic delivery of rAAV 6-microdystrophin preserves muscle function and extends lifespan in a murine model of severe muscular dystrophy (2014) (2)
Effect of Sildenafil on mdx Skeletal Muscle (2008) (2)
Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy (2013) (2)
Sildenafil Ameliorates Cardiomyopathy in mdx Mice (2009) (2)
Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy (2013) (1)
Erratum: Structural abnormalities at neuromuscular synapses lacking multiple syntrophin isoforms (Journal of Neuroscience (November 17, 2004) (10302-10309)) (2004) (1)
Association of acetylcholine receptors with peripheral membrane proteins: evidence from antibody-induced coaggregation (1994) (1)
Neurobiology. Synapses take the rap. (1995) (1)
Faculty Opinions recommendation of SynGAP regulates spine formation. (2004) (0)
611. Alpha-Dystrobrevin-3 Prevents Myopathy and Restores Diaphragm Function in the Alpha-Dystrobrevin Null Mouse (2015) (0)
solution structure of the joined PH domain of alpha1-syntrophin (2006) (0)
Faculty Opinions recommendation of Muscle-wide secretion of a miniaturized form of neural agrin rescues focal neuromuscular innervation in agrin mutant mice. (2008) (0)
Sildenafil ameliorates cardiomyopathy in dystrophin-null (mdx) mice (2009) (0)
Faculty Opinions recommendation of Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors. (2001) (0)
G.O.3 Mutations in contactin-1, a neuronal cell adhesion molecule expressed at the neuromuscular junction, cause a novel form of congenital lethal myopathy (2008) (0)
Characterization of the neuromuscular junction in patients with strabismus (2018) (0)
Croucher Advanced Study Institute (ASI) on Molecular Neuroscience (2002) (0)
Neurobiology. Anchoring glycine receptors. (1993) (0)
T.P.5 Sildenafil (Viagra®) improves cardiac and diaphragm muscle function in the dystrophic mouse (2012) (0)
muscular dystrophy The role of free radicals in the pathophysiology of (2015) (0)
PROPERTIES OF THE GLYCOPROTEIN LACCASE IMMOBILIZED BY TWO METHODS (1975) (0)
Developmental expression of syntrophin and dystrobrevin in human skeletal muscle (2002) (0)
Faculty Opinions recommendation of Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. (2002) (0)
Faculty Opinions recommendation of Localization of the calcitonin gene-related peptide receptor complex at the vertebrate neuromuscular junction and its role in regulating acetylcholinesterase expression. (2003) (0)
Faculty Opinions recommendation of Absence of acetylcholinesterase at the neuromuscular junctions of perlecan-null mice. (2002) (0)
Macromolecular Organization of the Neuromuscular Postsynaptic Membrane a (1989) (0)
Faculty Opinions recommendation of Neuregulin inhibits acetylcholine receptor aggregation in myotubes. (2004) (0)
solution structure of the split PH-PDZ Supramodule of alpha-Syntrophin (2006) (0)
TESIS DOCTORAL: “RESTORATION OF NNOSμ FUNCTION IN THE MDX MOUSE MODEL OF DUCHENNE MUSCULAR DYSTROPHY” (2013) (0)
Molecular targets for PDE inhibitor-mediated improvement of cardiac dysfunction in the mdx mouse? (2011) (0)
Oral 2022-1 - Defective skeletal muscle nNOS-cGMP signaling as a therapeutic target in Duchenne muscular dystrophy (2014) (0)
The 50 th Annual Meeting and Symposium of the Society of General Physiologists Cytoskeletal Regulation of Membrane Function ( organized by (1997) (0)
ARMS interacts with alpha-syntrophin: implications for the localization and signaling of EphA4 at the neuromuscular synapse (2005) (0)
Faculty Opinions recommendation of Treatment of ischemic brain damage by perturbing NMDA receptor- PSD-95 protein interactions. (2002) (0)
A Novel nNOS Signaling Pathway Regulates Skeletal Muscle Size, Strength and Fatigue Resistance (2008) (0)
An anti-peptide antibody specific for the class A calcium channel a , subunit labels mammalian neuromuscular junction ( synapses / voltage-dependent calcium channels / lmmunofluorescence / cerebelum ) (2004) (0)
Faculty Opinions recommendation of Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin. (2005) (0)
Nitric oxide regulates skeletal muscle performance by compartmentalization of nNOS splice variants (2009) (0)
Loss of nNOS Signaling Exacerbates Dystrophic Pathology, but not Skeletal Muscle Fatigue in the mdx Mouse Model of Duchenne Muscular Dystrophy (2010) (0)
Association of the Postsynaptic 43K Protein with Sites of Clustered and Diffusely-Distributed Acetylcholine Receptors (1986) (0)
Sildenafil Ameliorates Skeletal Muscle Pathology in the mdx Mouse Model of Duchenne Muscular Dystrophy (2011) (0)
John Paul Merlie (1945–1995) (1995) (0)
The Isolation, Purification and Characterization of Three RNA Polymerases from Novikoff Hepatoma Ascites Tumor (1973) (0)
Solution structure of the PDZ domain of alpha-syntrophin (2006) (0)
Cytoskeletal regulation of membrane function : Society of General Physiologists, 50th Annual Symposium, Marine Biological Laboratory, Woods Hole, Massachusetts, 5-7 September 1996 (1997) (0)
G.P.6.01 NPC1 overexpression attenuates muscular dystrophy in mdx and α-dystrobrevin-null mice (2007) (0)
Arms interacts with Alpha-syntrophin:Implications for EphA4 signaling at the neuromuscular synapse (2005) (0)
Functional specialization of retinal Müller cell endfeet depends on an interplay between two syntrophin isoforms (2020) (0)
Faculty Opinions recommendation of Crystal structure of the GABA(A)-receptor-associated protein, GABARAP. (2002) (0)
overloaded plantaris muscle upregulation of contractile protein mRNA in In vivo inhibition of nitric oxide synthase impairs (2015) (0)
Correction (1989) (0)
Nitric Oxide and its InteractionsPSS227 - nNOS is Necessary for Adaptive Hypertrophy and Resistance to Contraction-Induced Injury in the MDX Mouse Model of Duchenne Muscular Dystrophy (2013) (0)
G.O.24 Simvastatin improves physiological function and protects against muscle degeneration in mdx mice: A novel therapeutic approach for Duchenne muscular dystrophy (2015) (0)
G.P.350 Sarcolemmal nNOSµ targeting in mdx mice improves muscle function and restores dystrophin complex proteins via α-syntrophin (2015) (0)

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