Ueli Suter

Q: What Schools Are Affiliated With Ueli Suter

Ueli Suter is affiliated with the following schools: University of Lausanne, ETH Zurich, University of Basel, Kyoto University, University of Zurich

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Ueli Suter

Computer Science

#8819

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#9272

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Machine Learning

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#3761

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Artificial Intelligence

#4030

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#4088

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#5815

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#6032

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computer-science Degrees

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Computer Science

Ueli Suter's Degrees

PhD Computer Science ETH Zurich
Masters Computer Science University of Zurich
Bachelors Computer Science University of Zurich

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Ueli Suter'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

Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity (2012) (1118)
CNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination. (2010) (560)
The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A (1992) (506)
Schwann Cell Precursors from Nerve Innervation Are a Cellular Origin of Melanocytes in Skin (2009) (483)
Instructive Role of Wnt/ß-Catenin in Sensory Fate Specification in Neural Crest Stem Cells (2004) (429)
Trembler mouse carries a point mutation in a myelin gene (1992) (428)
Metabolic control of adult neural stem cell activity by Fasn-dependent lipogenesis (2012) (413)
Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network (2005) (397)
Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13) (1992) (396)
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice (1995) (369)
A Transgenic Rat Model of Charcot-Marie-Tooth Disease (1996) (359)
Disease mechanisms in inherited neuropathies (2003) (351)
Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling. (2001) (332)
Glial origin of mesenchymal stem cells in a tooth model system (2014) (327)
Lineage-specific requirements of β-catenin in neural crest development (2002) (327)
Neural crest–derived cells with stem cell features can be traced back to multiple lineages in the adult skin (2006) (320)
Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32 (1997) (313)
β1 integrins activate a MAPK signalling pathway in neural stem cells that contributes to their maintenance (2004) (307)
Jagged1-dependent Notch signaling is dispensable for hematopoietic stem cell self-renewal and differentiation. (2005) (299)
Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A) (2003) (296)
Elevated Phosphatidylinositol 3,4,5-Trisphosphate in Glia Triggers Cell-Autonomous Membrane Wrapping and Myelination (2010) (289)
A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. (1992) (289)
Steroid hormones and neurosteroids in normal and pathological aging of the nervous system (2003) (285)
Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells (2003) (277)
Notch1 is required for neuronal and glial differentiation in the cerebellum. (2002) (265)
Notch1 and its ligands Delta-like and Jagged are expressed and active in distinct cell populations in the postnatal mouse brain (2002) (253)
Impaired Differentiation of Schwann Cells in Transgenic Mice with Increased PMP22 Gene Dosage (1996) (236)
Molecular mechanisms regulating myelination in the peripheral nervous system (2012) (235)
A myelin protein is encoded by the homologue of a growth arrest-specific gene. (1991) (218)
Notch1 control of oligodendrocyte differentiation in the spinal cord (2002) (200)
Quantifying the Early Stages of Remyelination Following Cuprizone‐induced Demyelination (2003) (199)
Jagged1 signals in the postnatal subventricular zone are required for neural stem cell self‐renewal (2005) (193)
Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development (2007) (192)
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters. (1994) (190)
Dlg1-PTEN Interaction Regulates Myelin Thickness to Prevent Damaging Peripheral Nerve Overmyelination (2010) (190)
Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling (2005) (187)
Biology and genetics of hereditary motor and sensory neuropathies. (1995) (186)
The rat trk protooncogene product exhibits properties characteristic of the slow nerve growth factor receptor. (1992) (186)
Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot‐Marie‐Tooth disease) (2006) (176)
Progesterone Stimulates the Activity of the Promoters of Peripheral Myelin Protein‐22 and Protein Zero Genes in Schwann Cells (1998) (175)
Regulation of neural progenitor proliferation and survival by β1 integrins (2005) (166)
Epithelial Membrane Protein-1, Peripheral Myelin Protein 22, and Lens Membrane Protein 20 Define a Novel Gene Family * (1995) (165)
P0 and PMP22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-beta family factors. (1999) (162)
Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A (1993) (162)
Notch1 and Jagged1 are expressed after CNS demyelination, but are not a major rate-determining factor during remyelination. (2004) (158)
Two conserved domains in the NGF propeptide are necessary and sufficient for the biosynthesis of correctly processed and biologically active NGF. (1991) (157)
Heterozygous Peripheral Myelin Protein 22-Deficient Mice Are Affected by a Progressive Demyelinating Tomaculous Neuropathy (1997) (156)
HDAC1 and HDAC2 control the transcriptional program of myelination and the survival of Schwann cells (2011) (151)
Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease. (2002) (151)
Inactivation of TGFbeta signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome. (2005) (151)
Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot-Marie-Tooth disease type 4B1. (2002) (149)
E‐cadherin controls adherens junctions in the epidermis and the renewal of hair follicles (2003) (148)
Sox2 and Mitf cross-regulatory interactions consolidate progenitor and melanocyte lineages in the cranial neural crest (2012) (144)
Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease (2007) (141)
Multiple roles of mouse Numb in tuning developmental cell fates (2001) (139)
Genetically Induced Adult Oligodendrocyte Cell Death Is Associated with Poor Myelin Clearance, Reduced Remyelination, and Axonal Damage (2011) (136)
Cdc42 and Rac1 Signaling Are Both Required for and Act Synergistically in the Correct Formation of Myelin Sheaths in the CNS (2006) (135)
Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. (2007) (134)
Brain area-specific effect of TGF-beta signaling on Wnt-dependent neural stem cell expansion. (2008) (133)
Neurons Promote the Translocation of Peripheral Myelin Protein 22 into Myelin (1997) (132)
Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells. (1993) (131)
Balanced mTORC1 Activity in Oligodendrocytes Is Required for Accurate CNS Myelination (2014) (131)
Wnt/BMP signal integration regulates the balance between proliferation and differentiation of neuroepithelial cells in the dorsal spinal cord. (2007) (130)
The raft-associated protein MAL is required for maintenance of proper axon–glia interactions in the central nervous system (2004) (130)
Impaired Intracellular Trafficking Is a Common Disease Mechanism ofPMP22Point Mutations in Peripheral Neuropathies (1999) (128)
Compound developmental eye disorders following inactivation of TGFβ signaling in neural-crest stem cells (2005) (128)
GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance (2009) (122)
Many facets of the peripheral myelin protein PMP22 in myelination and disease (1998) (122)
Transport of Trembler-J Mutant Peripheral Myelin Protein 22 Is Blocked in the Intermediate Compartment and Affects the Transport of the Wild-Type Protein by Direct Interaction (1999) (121)
Molecular cell biology of Charcot-Marie-Tooth disease (2002) (121)
The peripheral myelin protein 22 and epithelial membrane protein family. (2000) (119)
ErbB2 Signaling in Schwann Cells Is Mostly Dispensable for Maintenance of Myelinated Peripheral Nerves and Proliferation of Adult Schwann Cells after Injury (2006) (117)
Aberrant Protein Trafficking inTremblerSuggests a Disease Mechanism for Hereditary Human Peripheral Neuropathies (1997) (117)
Integrin-linked kinase is required for radial sorting of axons and Schwann cell remyelination in the peripheral nervous system (2009) (116)
Dicer in Schwann Cells Is Required for Myelination and Axonal Integrity (2010) (116)
Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system (1993) (113)
Widespread expression of the peripheral myelin protein‐22 gene (pmp22) in neural and non‐neural tissues during murine development (1995) (113)
Zeb2 is essential for Schwann cell differentiation, myelination and nerve repair (2016) (112)
Stage-specific control of neural crest stem cell proliferation by the small rho GTPases Cdc42 and Rac1. (2009) (112)
Sox10 is required for Schwann‐cell homeostasis and myelin maintenance in the adult peripheral nerve (2011) (112)
Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module (2003) (112)
Temporal control of neural crest lineage generation by Wnt/β-catenin signaling (2012) (110)
β1-Integrin Signaling Mediates Premyelinating Oligodendrocyte Survival But Is Not Required for CNS Myelination and Remyelination (2006) (110)
SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system (2009) (104)
Peripheral myelin protein 22: Facts and hypotheses (1995) (103)
Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family. (1996) (103)
Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. (1995) (102)
Membrane-bound neuregulin1 type III actively promotes Schwann cell differentiation of multipotent Progenitor cells. (2002) (101)
mTORC1 controls PNS myelination along the mTORC1-RXRγ-SREBP-lipid biosynthesis axis in Schwann cells. (2014) (98)
Temporal control of neural crest lineage generation by Wnt/beta-catenin signaling (2012) (97)
Multi-level regulation of myotubularin-related protein-2 phosphatase activity by myotubularin-related protein-13/set-binding factor-2. (2006) (96)
Efficient Isolation and Gene Expression Profiling of Small Numbers of Neural Crest Stem Cells and Developing Schwann Cells (2004) (94)
Cholesterol and myelin. (1997) (93)
Injury-activated glial cells promote wound healing of the adult skin in mice (2018) (93)
Myelination and mTOR (2017) (91)
Nogo-A expressed in Schwann cells impairs axonal regeneration after peripheral nerve injury (2002) (89)
HDAC1 and HDAC2 Control the Specification of Neural Crest Cells into Peripheral Glia (2014) (89)
PMP22 Carrying the Trembler or Trembler-J Mutation Is Intracellularly Retained in Myelinating Schwann Cells (2000) (88)
Susceptible stages in Schwann cells for NF1-associated plexiform neurofibroma development. (2011) (87)
SH3TC2, a protein mutant in Charcot-Marie-Tooth neuropathy, links peripheral nerve myelination to endosomal recycling. (2010) (86)
Pals1 Is a Major Regulator of the Epithelial-Like Polarization and the Extension of the Myelin Sheath in Peripheral Nerves (2010) (84)
Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A. (2001) (83)
Charcot‐Marie‐Tooth disease‐associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission (2013) (81)
The function of RhoGTPases in axon ensheathment and myelination (2008) (80)
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes (2011) (78)
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models (2009) (75)
Identification of transcriptionally regulated genes after sciatic nerve injury (1991) (74)
Uncoupling of Myelin Assembly and Schwann Cell Differentiation by Transgenic Overexpression of Peripheral Myelin Protein 22 (2000) (73)
The Protooncogene Ski Controls Schwann Cell Proliferation and Myelination (2004) (71)
An animal model for Charcot-Marie-Tooth disease type 4B1. (2005) (70)
Stage-Specific Functions of the Small Rho GTPases Cdc42 and Rac1 for Adult Hippocampal Neurogenesis (2013) (69)
Autonomic neurogenesis and apoptosis are alternative fates of progenitor cell communities induced by TGFbeta. (2000) (69)
Differential Cyclin D1 Requirements of Proliferating Schwann Cells during Development and after Injury (2001) (69)
Akt/mTOR signalling in myelination. (2013) (67)
The Ets domain transcription factor Erm distinguishes rat satellite glia from Schwann cells and is regulated in satellite cells by neuregulin signaling. (2000) (66)
Analysis of neural crest–derived clones reveals novel aspects of facial development (2016) (65)
CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes (2019) (65)
Early Neuronal and Glial Fate Restriction of Embryonic Neural Stem Cells (2008) (65)
Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system (2017) (63)
FasL (CD95L/APO-1L) Resistance of Neurons Mediated by Phosphatidylinositol 3-Kinase-Akt/Protein Kinase B-Dependent Expression of Lifeguard/Neuronal Membrane Protein 35 (2005) (63)
Ultrastructural Distribution of PMP22 in Charcot‐Marie-Tooth Disease Type 1A (1996) (63)
The Small GTPase RhoA Is Required to Maintain Spinal Cord Neuroepithelium Organization and the Neural Stem Cell Pool (2011) (63)
The Gdap1 knockout mouse mechanistically links redox control to Charcot–Marie–Tooth disease (2014) (62)
Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation (2005) (61)
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2. (2007) (61)
Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain‐of‐function allele (1997) (61)
Dynamin 2 mutations in Charcot-Marie-Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination. (2012) (60)
Conduction Block in PMP22 Deficiency (2010) (60)
Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies (2000) (60)
Myelin is dependent on the Charcot–Marie–Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells (2012) (60)
Jagged1 Ablation Results in Cerebellar Granule Cell Migration Defects and Depletion of Bergmann Glia (2006) (59)
Disease mechanisms and potential therapeutic strategies in Charcot–Marie–Tooth disease (2001) (56)
The causes of Charcot-Marie-Tooth disease (2003) (56)
Injury signals cooperate with Nf1 loss to relieve the tumor-suppressive environment of adult peripheral nerve. (2013) (56)
Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1. (1996) (56)
Neural Membrane Protein 35 (NMP35): A Novel Member of a Gene Family Which Is Highly Expressed in the Adult Nervous System (1998) (55)
Targeting and Function of the Mitochondrial Fission Factor GDAP1 Are Dependent on Its Tail-Anchor (2009) (55)
Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom (2004) (53)
Abnormal junctions and permeability of myelin in PMP22‐deficient nerves (2014) (52)
Myelin and lymphocyte protein (MAL/MVP17/VIP17) and plasmolipin are members of an extended gene family. (1997) (51)
Molecular Basis of Common Hereditary Motor and Sensory Neuropathies in Humans and in Mouse Models (1995) (50)
NGF/BDNF chimeric proteins: analysis of neurotrophin specificity by homolog-scanning mutagenesis (1992) (48)
Transcriptional profiling of mouse peripheral nerves to the single-cell level to build a sciatic nerve ATlas (SNAT) (2021) (48)
Gpr126/Adgrg6 Has Schwann Cell Autonomous and Nonautonomous Functions in Peripheral Nerve Injury and Repair (2016) (47)
Optimal myelin elongation relies on YAP activation by axonal growth and inhibition by Crb3/Hippo pathway (2016) (47)
Combined HDAC1 and HDAC2 Depletion Promotes Retinal Ganglion Cell Survival After Injury Through Reduction of p53 Target Gene Expression (2015) (46)
AFM combines functional and morphological analysis of peripheral myelinated and demyelinated nerve fibers (2007) (45)
Murine numb regulates granule cell maturation in the cerebellum. (2004) (44)
Platelet‐derived growth factor‐BB supports the survival of cultured rat schwann cell precursors in synergy with neurotrophin‐3 (2000) (44)
The role of the Ets domain transcription factor Erm in modulating differentiation of neural crest stem cells. (2002) (43)
Cell cycle inhibitors p21 and p16 are required for the regulation of Schwann cell proliferation (2006) (43)
Profilin 1 is required for peripheral nervous system myelination (2014) (43)
Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease (2006) (43)
mTORC1 Is Transiently Reactivated in Injured Nerves to Promote c-Jun Elevation and Schwann Cell Dedifferentiation (2018) (43)
E-cadherin Is Required for the Correct Formation of Autotypic Adherens Junctions of the Outer Mesaxon but Not for the Integrity of Myelinated Fibers of Peripheral Nerves (2002) (43)
Cell-intrinsic and cell-extrinsic cues regulating lineage decisions in multipotent neural crest-derived progenitor cells. (2002) (42)
Embryonic expression of epithelial membrane protein 1 in early neurons. (1999) (42)
Understanding Schwann cell–neurone interactions: the key to Charcot–Marie–Tooth disease? * (2002) (42)
P 0 and PMP 22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-β family factors (1999) (40)
The Lin28/let-7 axis is critical for myelination in the peripheral nervous system (2015) (38)
De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination (2018) (38)
Distinct elements of the peripheral myelin protein 22 (PMP22) promoter regulate expression in Schwann cells and sensory neurons (2003) (37)
Neural membrane protein 35/Lifeguard is localized at postsynaptic sites and in dendrites. (2002) (37)
Gelsolin is required for macrophage recruitment during remyelination of the peripheral nervous system (2009) (37)
Dissecting Integrin-Dependent Regulation of Neural Stem Cell Proliferation in the Adult Brain (2014) (37)
Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot‐Marie‐Tooth disease type 1A (2002) (36)
Characterization of peripheral myelin protein 22 in zebrafish (zPMP22) suggests an early role in the development of the peripheral nervous system (1999) (35)
The carboxyl terminus of nerve growth factor is required for biological activity. (1993) (34)
The glycoprotein P0 in peripheral gliogenesis (1998) (34)
The genetics of myelin (1993) (33)
mTORC 1 Controls PNS Myelination along the mTORC 1-RXR gamma-SREBP-Lipid Biosynthesis Axis in Schwann Cells (33)
Progressive Segregation of Unmyelinated Axons in Peripheral Nerves, Myelin Alterations in the CNS, and Cyst Formation in the Kidneys of Myelin and Lymphocyte Protein‐Overexpressing Mice (2000) (33)
Effective gene transfer of lacZ and P0 into Schwann cells of P0‐deficient mice (1999) (32)
HDAC1/2-Dependent P0 Expression Maintains Paranodal and Nodal Integrity Independently of Myelin Stability through Interactions with Neurofascins (2015) (32)
The CMT4B disease-causing proteins MTMR2 and MTMR13/SBF2 regulate AKT signalling (2009) (31)
Embryonic gene expression resolved at the cellular level by fluorescence in situ hybridization (1999) (31)
Transgenic Mouse Models of CMT1A and HNPP (1999) (30)
Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves. (2013) (30)
Some applications of topological K-theory (1980) (29)
Postnatal Schwann cell proliferation but not myelination is strictly and uniquely dependent on cyclin-dependent kinase 4 (cdk4) (2008) (29)
Expression and localization of Ski determine cell type–specific TGFβ signaling effects on the cell cycle (2008) (29)
Signaling pathways mediating axon-Schwann cell interactions (1994) (29)
Mice Lacking Protease Nexin-1 Show Delayed Structural and Functional Recovery after Sciatic Nerve Crush (2007) (27)
Localization and functional roles of PMP22 in peripheral nerves of P0‐deficient mice (1999) (27)
How Histone Deacetylases Control Myelination (2011) (27)
Multicolor analysis of oligodendrocyte morphology, interactions, and development with Brainbow (2015) (26)
Neuromyotonia in mice with hereditary myelinopathies (2000) (26)
Glutathione-conjugating and membrane-remodeling activity of GDAP1 relies on amphipathic C-terminal domain (2016) (24)
Phosphoinositides and Charcot-Marie-Tooth disease: New keys to old questions (2007) (23)
Neuropathy in a human without the PMP22 gene. (2011) (23)
Identification of the regulatory region of the peripheral myelin protein 22 (PMP22) gene that directs temporal and spatial expression in development and regeneration of peripheral nerves. (2002) (23)
The “CMT Rat”: Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22 (1999) (22)
Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms (1997) (21)
Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3. (1999) (21)
Genetic basis of inherited peripheral neuropathies (1994) (21)
Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function (2019) (20)
Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene (1997) (18)
LITAF (SIMPLE) regulates Wallerian degeneration after injury but is not essential for peripheral nerve development and maintenance: Implications for Charcot‐Marie‐Tooth disease (2012) (18)
A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease (2011) (17)
Molecular biology of axon-glia interactions in the peripheral nervous system. (1997) (16)
Identification of the Regulatory Region of the Peripheral Myelin Protein 22 (PMP22) Gene That Directs Temporal and Spatial Expression in Development and Regeneration of Peripheral Nerves (2002) (16)
Characterization of GFP‐MAL expression and incorporation in rafts (2001) (15)
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models (2009) (15)
Molecular approaches to nerve regeneration. (1991) (15)
MRI signature in a novel mouse model of genetically induced adult oligodendrocyte cell death (2012) (14)
Dual function of the PI 3 K-Akt-mTORC 1 axis in myelination of the peripheral nervous system (2018) (13)
Neurological Mouse Mutants: A Molecular-Genetic Analysis of Myelin Proteins (2004) (13)
Antiprion prophylaxis by gene transfer of a soluble prion antagonist. (2008) (13)
Ral GTPases in Schwann cells promote radial axonal sorting in the peripheral nervous system (2019) (12)
Small Rho GTPases are key regulators of peripheral nerve biology in health and disease (2008) (11)
Gpr 126 / Adgrg 6 has Schwann cell autonomous and nonautonomous functions in peripheral nerve injury and repair (2017) (11)
Antigens expressed by myelinating glia cells induce peripheral cross‐tolerance of endogenous CD8+ T cells (2009) (10)
Isolation of transcriptionally regulated sequences associated with neuronal and non-neuronal cell interactions. (1992) (10)
PMP 22 Gene (2004) (9)
The Gdap 1 knockout mouse mechanistically links redox control to Charcot – Marie – Tooth disease (2014) (7)
The miRNA biogenesis pathway prevents inappropriate expression of injury response genes in developing and adult Schwann cells (2018) (7)
Models of Charcot-Marie-Tooth Disease (2004) (6)
Building lipids for myelin (2018) (5)
Chapter 19 – Myelination (2005) (5)
The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22. (1999) (5)
cell self-renewal and differentiation Jagged1 dependent Notch signaling is dispensable for hematopoietic stem (2013) (5)
Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy (2020) (5)
Connexin32 in hereditary neuropathies. (1999) (4)
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models (2009) (4)
Charcot-Marie-Tooth Disease: Pathology, Genetics, and Animal Models (1999) (3)
Author response: CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes (2019) (3)
N.I.3 Myelin and axons: Lessons learned from inherited peripheral neuropathies (2006) (2)
Characterization ofa Novel Peripheral Nervous System Myelin Protein (PMP22/SR13) (2002) (1)
Charcot-Marie-Tooth disease associated mutants of GDAP 1 dissociate its roles in peroxisomal and mitochondrial fission Running title : GDAP 1 in peroxisomal fission (2013) (1)
Chapter 32 The molecular basis of the neuropathies of mouse and human (1995) (1)
Molecular Biology of Hereditary Motor and Sensory Neuropathies (1997) (1)
QUANTIFYING THE EARLYSTAGES OF REMYELINATION FOLLOWING CUPRIZONE-INDUCEDDEMYELINATION (2003) (1)
On the vector field problem for product manifolds (1998) (1)
Defective hair formation in calcitonin‐like receptor transgenic mice (2008) (1)
The molecular basis of the neuropathies of mouse and human. (1995) (0)
Lineage-speciﬁc requirements of (cid:2) -catenin in neural crest development (2002) (0)
Molecular approaches towards the isolation of tyrosine phosphatases expressed in the peripheral nervous system. (1996) (0)
Wnt signaling instructively promotes sensory neurogenesis in early neural crest stem cells (2005) (0)
Wnt signaling instructively promotes sensory neurogenesis in early neural crest stem cells (2005) (0)
Involvement of ski in TGFbeta-induced proliferation of Schwann cells (2006) (0)
Dissecting of microenviromental nishes for OPC differentiation (2011) (0)
Ral GTPases are critical regulators of spinal cord myelination and homeostasis. (2022) (0)
Neuropathy in Human and Mice with PMP22 null (2013) (0)
Virtual Demyelination and Tight Junction Defect in PMP22 Deficiency (IN1-1.003) (2012) (0)
Injury-activated glial cells promote wound healing of the adult skin in mice (2018) (0)
Role of the IPP complex in myelination and remyelination (2010) (0)
Tumor and Stem Cell Biology Susceptible Stages in Schwann Cells for NF 1-Associated Plexiform Neurofibroma Development (2011) (0)
Early fate restriction of embryonic neural stem cells (2006) (0)
Faculty Opinions recommendation of Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10. (2002) (0)
Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms Volume 4, Numbers 3/4 (1997), pages 215–220 (doi:10.1006/nbdi.1997.0148) (2000) (0)
Promoter analysis of the CMT1A‐disease gene PMP22 in vivo (2008) (0)
Transgenic mouse models of CMT1A and HNPP. (1999) (0)
Edinburgh Research Explorer Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development (2018) (0)
Mechanical properties of myelinated and de-myelinated peripheral axons with the atomic force microscope (2004) (0)
Contents continued (2023) (0)
Faculty Opinions recommendation of Asymmetric inheritance of radial glial fibers by cortical neurons. (2001) (0)
On the exponent and the order of the groups $$\tilde J$$(X) (1978) (0)
T 2 RELAXATION PARALLELS PROGRESSIVE CLINICAL SYMPTOMS OF DEMYELINATION IN A NOVEL TRANSGENIC MOUSE MODEL (2008) (0)
Author response: Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function (2018) (0)
Erratum: SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system (Proceedings of the National Academy of Sciences of the United States of America (2009) 106, 41, (17528-17533) DOI: 10.1073/pnas.0905523106) (2010) (0)
Cotter Damaging Peripheral Nerve Overmyelination Dlg 1-PTEN Interaction Regulates Myelin Thickness to Prevent (2014) (0)
A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22 (2008) (0)
Disruption of Myelin Junctions and Increase of Myelin Permeability in PMP22 Deficiency (P1.065) (2014) (0)
Author response: Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system (2017) (0)
Role of dbpA in neural crest and Schwann cell development (2006) (0)
Correction for SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system (2010) (0)

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