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Search results 1 to 100 out of 343 for Uchl1

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Category: Publication
Type Details Score
Publication
First Author: Jara JH
Year: 2013
Journal: Cell Biochem Biophys
Title: Could dysregulation of UPS be a common underlying mechanism for cancer and neurodegeneration? Lessons from UCHL1.
Volume: 67
Issue: 1
Pages: 45-53
Publication
First Author: Setsuie R
Year: 2007
Journal: Neurochem Int
Title: The functions of UCH-L1 and its relation to neurodegenerative diseases.
Volume: 51
Issue: 2-4
Pages: 105-11
Publication
First Author: Proctor CJ
Year: 2010
Journal: PLoS One
Title: Modelling the role of UCH-L1 on protein aggregation in age-related neurodegeneration.
Volume: 5
Issue: 10
Pages: e13175
Publication
First Author: Gao H
Year: 2020
Journal: PLoS One
Title: UCHL1 regulates oxidative activity in skeletal muscle.
Volume: 15
Issue: 11
Pages: e0241716
Publication  
First Author: Antony R
Year: 2022
Journal: Front Physiol
Title: UCHL1 Regulates Lipid and Perilipin 2 Level in Skeletal Muscle.
Volume: 13
Pages: 855193
Publication  
First Author: Gao H
Year: 2019
Journal: Life Sci
Title: UCHL1 regulates muscle fibers and mTORC1 activity in skeletal muscle.
Volume: 233
Pages: 116699
Publication
First Author: Carrieri C
Year: 2012
Journal: Nature
Title: Long non-coding antisense RNA controls Uchl1 translation through an embedded SINEB2 repeat.
Volume: 491
Issue: 7424
Pages: 454-7
Publication  
First Author: Coulombe J
Year: 2014
Journal: Front Aging Neurosci
Title: Loss of UCHL1 promotes age-related degenerative changes in the enteric nervous system.
Volume: 6
Pages: 129
Publication
First Author: Hao L
Year: 2020
Journal: Histochem Cell Biol
Title: Gene UCHL1 expresses specifically in mouse uterine decidual cells in response to estrogen.
Volume: 154
Issue: 3
Pages: 275-286
Publication      
First Author: Liu H
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Role of UCHL1 in axonal injury and functional recovery after cerebral ischemia.
Publication
First Author: Costes S
Year: 2014
Journal: Autophagy
Title: UCHL1 deficiency exacerbates human islet amyloid polypeptide toxicity in β-cells: evidence of interplay between the ubiquitin/proteasome system and autophagy.
Volume: 10
Issue: 6
Pages: 1004-14
Publication
First Author: Jara JH
Year: 2015
Journal: Cereb Cortex
Title: Corticospinal Motor Neurons Are Susceptible to Increased ER Stress and Display Profound Degeneration in the Absence of UCHL1 Function.
Volume: 25
Issue: 11
Pages: 4259-72
Publication      
First Author: Karst SY
Year: 2010
Journal: MGI Direct Data Submission
Title: Gracile axonal dystrophy 2 Jackson; a neuromuscular mutation in the Uchl1 gene
Publication
First Author: Genç B
Year: 2022
Journal: Gene Ther
Title: Upper motor neurons are a target for gene therapy and UCHL1 is necessary and sufficient to improve cellular integrity of diseased upper motor neurons.
Volume: 29
Issue: 3-4
Pages: 178-192
Publication
First Author: Setsuie R
Year: 2007
Journal: Neurochem Int
Title: Dopaminergic neuronal loss in transgenic mice expressing the Parkinson's disease-associated UCH-L1 I93M mutant.
Volume: 50
Issue: 1
Pages: 119-29
Publication
First Author: Yasuda T
Year: 2009
Journal: J Neurochem
Title: Effects of UCH-L1 on alpha-synuclein over-expression mouse model of Parkinson's disease.
Volume: 108
Issue: 4
Pages: 932-44
Publication
First Author: Wiese CB
Year: 2013
Journal: Genesis
Title: A Uchl1-Histone2BmCherry:GFP-gpi BAC transgene for imaging neuronal progenitors.
Volume: 51
Issue: 12
Pages: 852-61
Publication
First Author: Wang Y
Year: 2000
Journal: Genomics
Title: YAC/BAC-based physical and transcript mapping around the gracile axonal dystrophy (gad) locus identifies Uchl1, Pmx2b, Atp3a2, and Hip2 genes.
Volume: 66
Issue: 3
Pages: 333-6
Publication
First Author: Read NC
Year: 2014
Journal: Biochim Biophys Acta
Title: Ubiquitin C-terminal hydrolase L1 deletion ameliorates glomerular injury in mice with ACTN4-associated focal segmental glomerulosclerosis.
Volume: 1842
Issue: 7
Pages: 1028-40
Publication
First Author: Koyanagi S
Year: 2012
Journal: Reproduction
Title: Effects of ubiquitin C-terminal hydrolase L1 deficiency on mouse ova.
Volume: 143
Issue: 3
Pages: 271-9
Publication
First Author: Zhang M
Year: 2012
Journal: J Neurochem
Title: Control of BACE1 degradation and APP processing by ubiquitin carboxyl-terminal hydrolase L1.
Volume: 120
Issue: 6
Pages: 1129-38
Publication
First Author: Lei Q
Year: 2020
Journal: Sci Rep
Title: Ubiquitin C-terminal hydrolase L1 (UCHL1) regulates post-myocardial infarction cardiac fibrosis through glucose-regulated protein of 78 kDa (GRP78).
Volume: 10
Issue: 1
Pages: 10604
Publication  
First Author: Mi Z
Year: 2021
Journal: Neuroscience
Title: Mutation of a Ubiquitin Carboxy Terminal Hydrolase L1 Lipid Binding Site Alleviates Cell Death, Axonal Injury, and Behavioral Deficits After Traumatic Brain Injury in Mice.
Volume: 475
Pages: 127-136
Publication
First Author: Chu KY
Year: 2012
Journal: Diabetologia
Title: Ubiquitin C-terminal hydrolase L1 is required for pancreatic beta cell survival and function in lipotoxic conditions.
Volume: 55
Issue: 1
Pages: 128-40
Publication  
First Author: Mi Z
Year: 2021
Journal: Exp Neurol
Title: Abolishing UCHL1's hydrolase activity exacerbates TBI-induced axonal injury and neuronal death in mice.
Volume: 336
Pages: 113524
Publication
First Author: Woodman MF
Year: 2022
Journal: Biol Reprod
Title: The requirement of ubiquitin C-terminal hydrolase L1 in mouse ovarian development and fertility†.
Volume: 107
Issue: 2
Pages: 500-513
Publication
First Author: Hussain S
Year: 2018
Journal: Blood
Title: UCH-L1 bypasses mTOR to promote protein biosynthesis and is required for MYC-driven lymphomagenesis in mice.
Volume: 132
Issue: 24
Pages: 2564-2574
Publication  
First Author: Wu P
Year: 2022
Journal: Front Cardiovasc Med
Title: Ubiquitin Carboxyl-Terminal Hydrolase L1 of Cardiomyocytes Promotes Macroautophagy and Proteostasis and Protects Against Post-myocardial Infarction Cardiac Remodeling and Heart Failure.
Volume: 9
Pages: 866901
Publication
First Author: Saigoh K
Year: 1999
Journal: Nat Genet
Title: Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice.
Volume: 23
Issue: 1
Pages: 47-51
Publication
First Author: Marzban G
Year: 2002
Journal: Exp Gerontol
Title: Age-related alterations in the protein expression profile of C57BL/6J mouse pituitaries.
Volume: 37
Issue: 12
Pages: 1451-60
Publication
First Author: Harada T
Year: 2004
Journal: Am J Pathol
Title: Role of ubiquitin carboxy terminal hydrolase-L1 in neural cell apoptosis induced by ischemic retinal injury in vivo.
Volume: 164
Issue: 1
Pages: 59-64
Publication
First Author: Sakurai M
Year: 2008
Journal: Eur J Neurosci
Title: Reduction in memory in passive avoidance learning, exploratory behaviour and synaptic plasticity in mice with a spontaneous deletion in the ubiquitin C-terminal hydrolase L1 gene.
Volume: 27
Issue: 3
Pages: 691-701
Publication
First Author: Bedekovics T
Year: 2016
Journal: Blood
Title: UCH-L1 is induced in germinal center B cells and identifies patients with aggressive germinal center diffuse large B-cell lymphoma.
Volume: 127
Issue: 12
Pages: 1564-74
Publication
First Author: Yamazaki K
Year: 1992
Journal: Jikken Dobutsu
Title: Behavioral study on the gracile axonal dystrophy (GAD) mutant mouse.
Volume: 41
Issue: 4
Pages: 523-7
Publication
First Author: Pfeffer M
Year: 2012
Journal: Neurobiol Aging
Title: Disturbed sleep/wake rhythms and neuronal cell loss in lateral hypothalamus and retina of mice with a spontaneous deletion in the ubiquitin carboxyl-terminal hydrolase L1 gene.
Volume: 33
Issue: 2
Pages: 393-403
Publication
First Author: Wang YL
Year: 2006
Journal: Mol Reprod Dev
Title: Overexpression of ubiquitin carboxyl-terminal hydrolase L1 arrests spermatogenesis in transgenic mice.
Volume: 73
Issue: 1
Pages: 40-9
Publication
First Author: Yamazaki K
Year: 1988
Journal: Proc Soc Exp Biol Med
Title: Gracile axonal dystrophy (GAD), a new neurological mutant in the mouse.
Volume: 187
Issue: 2
Pages: 209-15
Publication
First Author: Mukoyama M
Year: 1989
Journal: Acta Neuropathol
Title: Neuropathology of gracile axonal dystrophy (GAD) mouse. An animal model of central distal axonopathy in primary sensory neurons.
Volume: 79
Issue: 3
Pages: 294-9
Publication
First Author: Takagi A
Year: 1996
Journal: Virchows Arch
Title: Fine structural changes of muscle spindles in the gracile axonal dystrophy mutant mouse.
Volume: 428
Issue: 4-5
Pages: 289-96
Publication
First Author: Yamazaki K
Year: 1993
Journal: Mol Chem Neuropathol
Title: Substance P-immunoreactive astrocytes in gracile sensory nervous tract of spinal cord in gracile axonal dystrophy mutant mouse.
Volume: 20
Issue: 1
Pages: 1-20
Publication
First Author: Xilouri M
Year: 2012
Journal: Hum Mol Genet
Title: Selective neuroprotective effects of the S18Y polymorphic variant of UCH-L1 in the dopaminergic system.
Volume: 21
Issue: 4
Pages: 874-89
Publication
First Author: Suh JG
Year: 1994
Journal: Biomed Res
Title: Pathophysiological study of axonal degeneration in the gracile axonal dystrophy (gad) mutant mouse.
Volume: 15
Issue: 4
Pages: 241-246
Publication
First Author: Miura H
Year: 1993
Journal: Neuropathol Appl Neurobiol
Title: Progressive degeneration of motor nerve terminals in GAD mutant mouse with hereditary sensory axonopathy.
Volume: 19
Issue: 1
Pages: 41-51
Publication
First Author: Chandran AP
Year: 1995
Journal: Electromyogr Clin Neurophysiol
Title: Stimulus induced repetitive muscle potentials in the gracile axonal dystrophy (GAD) mouse.
Volume: 35
Issue: 4
Pages: 225-30
Publication
First Author: Yamazaki K
Year: 1994
Journal: Neurosci Lett
Title: Methylcobalamin (methyl-B12) promotes regeneration of motor nerve terminals degenerating in anterior gracile muscle of gracile axonal dystrophy (GAD) mutant mouse.
Volume: 170
Issue: 1
Pages: 195-7
Publication
First Author: Cartier AE
Year: 2009
Journal: J Neurosci
Title: Regulation of synaptic structure by ubiquitin C-terminal hydrolase L1.
Volume: 29
Issue: 24
Pages: 7857-68
Publication
First Author: Chen F
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Ubiquitin carboxyl-terminal hydrolase L1 is required for maintaining the structure and function of the neuromuscular junction.
Volume: 107
Issue: 4
Pages: 1636-41
Publication  
First Author: Alpaugh WF
Year: 2021
Journal: Cells
Title: Loss of Ubiquitin Carboxy-Terminal Hydrolase L1 Impairs Long-Term Differentiation Competence and Metabolic Regulation in Murine Spermatogonial Stem Cells.
Volume: 10
Issue: 9
Publication
First Author: Li JC
Year: 2000
Journal: World J Gastroenterol
Title: Immunohistochemical study on gastroenteric nervous system in trisomy 16 mice:an animal model of Down syndrome.
Volume: 6
Issue: 6
Pages: 793-799
Publication
First Author: Schofield JN
Year: 1995
Journal: Brain Res Dev Brain Res
Title: PGP9.5, a ubiquitin C-terminal hydrolase; pattern of mRNA and protein expression during neural development in the mouse.
Volume: 85
Issue: 2
Pages: 229-38
Publication
First Author: Suh JG
Year: 1995
Journal: Genomics
Title: Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5.
Volume: 27
Issue: 3
Pages: 549-51
Publication
First Author: Sekiguchi S
Year: 2003
Journal: Exp Anim
Title: Immunohistochemical analysis of protein gene product 9.5, a ubiquitin carboxyl-terminal hydrolase, during placental and embryonic development in the mouse.
Volume: 52
Issue: 4
Pages: 365-9
Publication
First Author: Li JC
Year: 2001
Journal: World J Gastroenterol
Title: The development of colon innervation in trisomy 16 mice and Hirschsprung's disease.
Volume: 7
Issue: 1
Pages: 16-21
Publication
First Author: Lohmann F
Year: 2014
Journal: Biochim Biophys Acta
Title: UCH-L1 induces podocyte hypertrophy in membranous nephropathy by protein accumulation.
Volume: 1842
Issue: 7
Pages: 945-58
Publication
First Author: Reinicke AT
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Ubiquitin C-terminal hydrolase L1 (UCH-L1) loss causes neurodegeneration by altering protein turnover in the first postnatal weeks.
Volume: 116
Issue: 16
Pages: 7963-7972
Publication
First Author: Radón V
Year: 2018
Journal: Kidney Int
Title: Ubiquitin C-Terminal Hydrolase L1 is required for regulated protein degradation through the ubiquitin proteasome system in kidney.
Volume: 93
Issue: 1
Pages: 110-127
Publication
First Author: Reinicke AT
Year: 2019
Journal: J Immunol
Title: Deubiquitinating Enzyme UCH-L1 Promotes Dendritic Cell Antigen Cross-Presentation by Favoring Recycling of MHC Class I Molecules.
Volume: 203
Issue: 7
Pages: 1730-1742
Publication
First Author: Osaka H
Year: 2003
Journal: Hum Mol Genet
Title: Ubiquitin carboxy-terminal hydrolase L1 binds to and stabilizes monoubiquitin in neuron.
Volume: 12
Issue: 16
Pages: 1945-58
Publication
First Author: Walters BJ
Year: 2008
Journal: Mol Cell Neurosci
Title: Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity.
Volume: 39
Issue: 4
Pages: 539-48
Publication
First Author: Kon Y
Year: 1999
Journal: Mol Reprod Dev
Title: Expression of protein gene product 9.5, a neuronal ubiquitin C-terminal hydrolase, and its developing change in sertoli cells of mouse testis.
Volume: 54
Issue: 4
Pages: 333-41
Publication
First Author: Zlatic SA
Year: 2018
Journal: Cell Syst
Title: Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees.
Volume: 6
Issue: 3
Pages: 368-380.e6
Publication
First Author: Kwon J
Year: 2006
Journal: Exp Anim
Title: The region-specific functions of two ubiquitin C-terminal hydrolase isozymes along the epididymis.
Volume: 55
Issue: 1
Pages: 35-43
Publication
First Author: Sekiguchi S
Year: 2006
Journal: Am J Pathol
Title: Localization of ubiquitin C-terminal hydrolase L1 in mouse ova and its function in the plasma membrane to block polyspermy.
Volume: 169
Issue: 5
Pages: 1722-9
Publication
First Author: Kwon J
Year: 2004
Journal: Am J Pathol
Title: Two closely related ubiquitin C-terminal hydrolase isozymes function as reciprocal modulators of germ cell apoptosis in cryptorchid testis.
Volume: 165
Issue: 4
Pages: 1367-74
Publication
First Author: Kurihara LJ
Year: 2001
Journal: Hum Mol Genet
Title: Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia.
Volume: 10
Issue: 18
Pages: 1963-70
Publication
First Author: Oda K
Year: 1992
Journal: Neuropathol Appl Neurobiol
Title: Dying back type axonal degeneration of sensory nerve terminals in muscle spindles of the gracile axonal dystrophy (GAD) mutant mouse.
Volume: 18
Issue: 3
Pages: 265-81
Publication
First Author: Suh JG
Year: 1994
Journal: Lab Anim Sci
Title: Breeding of the gad-mdx mouse: influence of genetically induced denervation on dystrophic muscle fibers.
Volume: 44
Issue: 1
Pages: 42-6
Publication
First Author: Matsushima Y
Year: 2005
Journal: Mamm Genome
Title: A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1.
Volume: 16
Issue: 2
Pages: 73-8
Publication  
First Author: Shimshek DR
Year: 2012
Journal: Sci Rep
Title: Excess α-synuclein worsens disease in mice lacking ubiquitin carboxy-terminal hydrolase L1.
Volume: 2
Pages: 262
Publication
First Author: Matsui K
Year: 1994
Journal: Neurosci Lett
Title: Developmental changes of nerve growth factor levels in the gracile axonal dystrophy mouse.
Volume: 177
Issue: 1-2
Pages: 116-8
Publication
First Author: Kwon J
Year: 2003
Journal: Exp Anim
Title: Characterization of the testis in congenitally ubiquitin carboxy-terminal hydrolase-1 (Uch-L1) defective (gad) mice.
Volume: 52
Issue: 1
Pages: 1-9
Publication
First Author: Boisvert NC
Year: 2018
Journal: Am J Physiol Renal Physiol
Title: Ubiquitin COOH-terminal hydrolase L1 deletion is associated with urinary α-klotho deficiency and perturbed phosphate homeostasis.
Volume: 315
Issue: 2
Pages: F353-F363
Publication
First Author: Løes S
Year: 2002
Journal: Anat Embryol (Berl)
Title: Mouse rudimentary diastema tooth primordia are devoid of peripheral nerve fibers.
Volume: 205
Issue: 3
Pages: 187-91
Publication
First Author: Sidebotham EL
Year: 2001
Journal: Pediatr Surg Int
Title: Assessment of protein gene product 9.5 as a marker of neural crest-derived precursor cells in the developing enteric nervous system.
Volume: 17
Issue: 4
Pages: 304-7
Publication
First Author: Guembe L
Year: 1999
Journal: Am J Respir Cell Mol Biol
Title: Histochemical demonstration of neuronal nitric oxide synthase during development of mouse respiratory tract.
Volume: 20
Issue: 2
Pages: 342-51
Publication
First Author: Jitpukdeebodintra S
Year: 2002
Journal: Int J Dev Biol
Title: Developmental patterning of the circumvallate papilla.
Volume: 46
Issue: 5
Pages: 755-63
Publication
First Author: Woodward MN
Year: 2003
Journal: J Pediatr Surg
Title: Analysis of the effects of endothelin-3 on the development of neural crest cells in the embryonic mouse gut.
Volume: 38
Issue: 9
Pages: 1322-8
Publication
First Author: Zhu S
Year: 2008
Journal: J Histochem Cytochem
Title: Immunolocalization of Periostin-like factor and Periostin during embryogenesis.
Volume: 56
Issue: 4
Pages: 329-45
Publication
First Author: Osbun N
Year: 2011
Journal: Am J Med Genet A
Title: Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.
Volume: 155A
Issue: 8
Pages: 1865-76
Publication
First Author: Guo YY
Year: 2017
Journal: J Neurosci
Title: Ubiquitin C-Terminal Hydrolase L1 (UCH-L1) Promotes Hippocampus-Dependent Memory via Its Deubiquitinating Effect on TrkB.
Volume: 37
Issue: 25
Pages: 5978-5995
Publication
First Author: Tsuru M
Year: 2018
Journal: PLoS One
Title: Ubiquitin-dependent proteolysis of CXCL7 leads to posterior longitudinal ligament ossification.
Volume: 13
Issue: 5
Pages: e0196204
Publication
First Author: Gong SG
Year: 2001
Journal: Differentiation
Title: Characterization of olfactory nerve abnormalities in Twirler mice.
Volume: 69
Issue: 1
Pages: 58-65
Publication
First Author: Dillon TE
Year: 2004
Journal: J Comp Neurol
Title: Sema3A regulates the timing of target contact by cranial sensory axons.
Volume: 470
Issue: 1
Pages: 13-24
Publication
First Author: Greer JM
Year: 2002
Journal: Neuron
Title: Hoxb8 is required for normal grooming behavior in mice.
Volume: 33
Issue: 1
Pages: 23-34
Publication  
First Author: Yamazaki K
Year: 1987
Journal: Jpn J Genet
Title: Location of gracile axonal dystrophy (gad) on Chromosome 5 of the mouse
Volume: 62
Pages: 479-84
Publication
First Author: Ichihara N
Year: 1995
Journal: Brain Res
Title: Axonal degeneration promotes abnormal accumulation of amyloid beta-protein in ascending gracile tract of gracile axonal dystrophy (GAD) mouse.
Volume: 695
Issue: 2
Pages: 173-8
Publication
First Author: Wang YL
Year: 2004
Journal: Brain Res
Title: Accumulation of beta- and gamma-synucleins in the ubiquitin carboxyl-terminal hydrolase L1-deficient gad mouse.
Volume: 1019
Issue: 1-2
Pages: 1-9
Publication
First Author: Kameda Y
Year: 2004
Journal: J Histochem Cytochem
Title: The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse.
Volume: 52
Issue: 5
Pages: 641-51
Publication
First Author: Wakisaka S
Year: 1996
Journal: Anat Embryol (Berl)
Title: Protein gene-product 9.5 in developing mouse circumvallate papilla: comparison with neuron-specific enolase and calcitonin gene-related peptide.
Volume: 194
Issue: 4
Pages: 365-72
Publication
First Author: Bitoh Y
Year: 2002
Journal: J Pediatr Surg
Title: Development of the pelvic floor muscles of murine embryos with anorectal malformations.
Volume: 37
Issue: 2
Pages: 224-7
Publication
First Author: Ratcliffe EM
Year: 2006
Journal: J Comp Neurol
Title: Netrin/DCC-mediated attraction of vagal sensory axons to the fetal mouse gut.
Volume: 498
Issue: 5
Pages: 567-80
Publication
First Author: Kim JY
Year: 2011
Journal: FEBS Lett
Title: Ubiquitin C-terminal hydrolase-L3 regulates Smad1 ubiquitination and osteoblast differentiation.
Volume: 585
Issue: 8
Pages: 1121-6
Publication
First Author: Sugimoto T
Year: 2015
Journal: Anat Rec (Hoboken)
Title: Three-Dimensional Visualization of Developing Neurovascular Architecture in the Craniofacial Region of Embryonic Mice.
Volume: 298
Issue: 11
Pages: 1824-35
Publication
First Author: Hasegawa H
Year: 2007
Journal: J Neurosci
Title: Analyzing somatosensory axon projections with the sensory neuron-specific Advillin gene.
Volume: 27
Issue: 52
Pages: 14404-14
Publication
First Author: Aruga J
Year: 2003
Journal: Gene Expr Patterns
Title: Slitrk6 expression profile in the mouse embryo and its relationship to that of Nlrr3.
Volume: 3
Issue: 6
Pages: 727-33
Publication
First Author: Horiguchi S
Year: 2010
Journal: Biochem Biophys Res Commun
Title: Downregulation of msh-like 2 (msx2) and neurotrophic tyrosine kinase receptor type 2 (ntrk2) in the developmental gut of KIT mutant mice.
Volume: 396
Issue: 3
Pages: 774-9
Publication
First Author: Hellard D
Year: 2004
Journal: Dev Biol
Title: Cranial sensory neuron development in the absence of brain-derived neurotrophic factor in BDNF/Bax double null mice.
Volume: 275
Issue: 1
Pages: 34-43
Publication
First Author: Suzuki Y
Year: 2010
Journal: Cell Tissue Res
Title: Regulatory role of Six1 in the development of taste papillae.
Volume: 339
Issue: 3
Pages: 513-25
Publication
First Author: Engleka KA
Year: 2005
Journal: Dev Biol
Title: Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives.
Volume: 280
Issue: 2
Pages: 396-406
Publication  
First Author: Gou-Fàbregas M
Year: 2016
Journal: Sci Rep
Title: 7-dehydrocholesterol efficiently supports Ret signaling in a mouse model of Smith-Opitz-Lemli syndrome.
Volume: 6
Pages: 28534