|  Help  |  About  |  Contact Us

Search our database by keyword

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 6701 to 6800 out of 7240 for Mb

0.04s

Categories

Hits by Pathway

Hits by Category

Hits by Strain

Type Details Score
Publication
First Author: Migliavacca E
Year: 2015
Journal: Am J Hum Genet
Title: A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.
Volume: 96
Issue: 5
Pages: 784-96
Publication
First Author: Blumenthal I
Year: 2014
Journal: Am J Hum Genet
Title: Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
Volume: 94
Issue: 6
Pages: 870-83
Genotype
Symbol: Kif5a/Kif5a Tg(Syn1-cre)671Jxm/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Chd4/Chd4 Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Lck-cre)1Cwi/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Ts(17<16>)65Dn/? Del(16Cbr1-Fam3b)1Rhr/?
Background: involves: 129S6/SvEvTac * C57BL/6 * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Dp(11Cops3-Rnf112)1Jrl/? Tyr/Tyr
Background: B6Brd.Cg-Tyr Dp(11Cops3-Rnf112)1Jrl
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tsc1/Tsc1 Tg(Syn1-cre)671Jxm/?
Background: involves: 129S4/SvJae * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Dsg4/Dsg4 Fas/Fas Yaa/?
Background: EOD-Dsg4
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Foxq1/Foxq1<+> Sox4/Sox4<+> Del(13)36H/?
Background: involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Ntrk2/Ntrk2 Slc1a3/? Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129/Sv * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Itga3/Itga3 Tg(CAG-Bgeo/GFP)21Lbe/? Tg(SFTPC-rtTA)5Jaw/? Tg(tetO-cre)1Jaw/?
Background: involves: 129 * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Ucp2/Ucp2 Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pmch-cre)1Lowl/?
Background: involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * FVB/NJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Nkx6-1/Nkx6-1 Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Neurog3-cre)C1Able/?
Background: involves: 129/Sv * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Wdr35/Wdr35
Background: involves: C57BL/6N
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: Ostm1/Ostm1
Background: involves: C3HeB/FeJ
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: M1185b/+ Del(13)36H/? Foxq1/Foxq1<+>
Background: involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Atoh7/Atoh7<+> Tg(Atoh7-cre)360Gla/? Tg(CAG-Bgeo/GFP)21Lbe/?
Background: either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL)
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Atoh7/Atoh7 Tg(Atoh7-cre)360Gla/? Tg(CAG-Bgeo/GFP)21Lbe/?
Background: either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL)
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Clstn3/Clstn3 Tg(Syn1-cre)671Jxm/?
Background: involves: C57BL/6 * C57BL/6N * CBA * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Gad1/Gad1<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Rbpj/Rbpj<+> Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pax6-cre,GFP)2Pgr/?
Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Rbpj/Rbpj Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pax6-cre,GFP)2Pgr/?
Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Mog/Mog<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Kera-cre)KC4.3Wwk/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Nes-cre)1Kln/?
Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Ifi208/Ifi208<+>
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Hspa2-cre)1Eddy/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pax2-cre)1Akg/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(GFAP-cre/Esr1*,-lacZ)ASbk/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(GFAP-cre/Esr1*,-lacZ)BSbk/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Neurog1-cre)1Jejo/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(CAG-cre/Esr1*)1Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Meox2/Meox2<+> Tg(Ttr-RFP)1Hadj/?
Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Nppa-cre)4Vmc/?
Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Nppa-cre)3Vmc/?
Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Mcm2/Mcm2<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Slc17a6-icre)1Oki/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Nr2e1-cre/ERT2)1Gsc/?
Background: involves: 129S1/Sv * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Cspg4-cre/Esr1*)BAkik/?
Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Neurog3-cre)C1Able/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Syn1-cre)671Jxm/?
Background: B6.Cg-Gt(ROSA)26Sor Tg(Syn1-cre)671Jxm
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Jdp2-cre)#Kkyo/?
Background: involves: 129S1/Sv * 129X1/SvJ * FVB/N
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Cck-cre,-lacZ)1Mini/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Ntrk2/Ntrk2 Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Cck-cre,-lacZ)1Mini/?
Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Agrp/Agrp<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Foxa2/Sox9-cre,-lacZ)#Vleu/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Kiss1-cre)J2-4Cfe/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Opn4/Opn4<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pmch-cre)1Lowl/?
Background: involves: 129S1/Sv * 129X1/SvJ * FVB/NJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Pdgfra-cre/ERT)467Dbe/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Tg(CAG-Bgeo/GFP)21Lbe/? Tg(Zbtb16-mCherry,-cre/ERT2)#Rhob/?
Background: involves: 129S1/Sv * 129X1/SvJ
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: E2f1/E2f1<+> Tg(CAG-Bgeo/GFP)21Lbe/?
Background: involves: 129S1/Sv * 129X1/SvJ * ARC * C3H * C57BL/6
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Rheb/Rheb Rpl22/Rpl22<+> Tg(Syn1-cre)671Jxm/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Slc39a8/Slc39a8 Tg(Syn1-cre)671Jxm/?
Background: involves: C57BL/6 * C57BL/6N * CBA
Zygosity: cn
Has Mutant Allele: true
Publication
First Author: Liu S
Year: 2004
Journal: Mol Cell Biol
Title: Identification of the proteins required for biosynthesis of diphthamide, the target of bacterial ADP-ribosylating toxins on translation elongation factor 2.
Volume: 24
Issue: 21
Pages: 9487-97
Protein
Organism: Mus musculus/domesticus
Length: 419  
Fragment?: false
Publication  
First Author: Hernandez-Moran BA
Year: 2022
Journal: Genes (Basel)
Title: Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse.
Volume: 13
Issue: 10
Publication
First Author: Malo D
Year: 1994
Journal: Genomics
Title: Haplotype mapping and sequence analysis of the mouse Nramp gene predict susceptibility to infection with intracellular parasites.
Volume: 23
Issue: 1
Pages: 51-61
Publication  
First Author: Puk O
Year: 2013
Journal: Mol Vis
Title: Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon.
Volume: 19
Pages: 877-84
Publication
First Author: Gong B
Year: 2022
Journal: J Neuroinflammation
Title: Complement C3a activates astrocytes to promote medulloblastoma progression through TNF-α.
Volume: 19
Issue: 1
Pages: 159
Publication
First Author: Mohan S
Year: 2005
Journal: J Bone Miner Res
Title: Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.
Volume: 20
Issue: 9
Pages: 1597-610
Publication
First Author: King R
Year: 2018
Journal: PLoS Genet
Title: Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.
Volume: 14
Issue: 1
Pages: e1007145
Publication
First Author: Feldman G
Year: 2017
Journal: J Transl Med
Title: A murine model for developmental dysplasia of the hip: ablation of CX3CR1 affects acetabular morphology and gait.
Volume: 15
Issue: 1
Pages: 233
Publication      
First Author: Gagnon LH
Year: 2017
Journal: MGI Direct Data Submission
Title: The pvt mutation
Publication
First Author: Edderkaoui B
Year: 2006
Journal: J Bone Miner Res
Title: Multiple genetic loci from CAST/EiJ chromosome 1 affect vBMD either positively or negatively in a C57BL/6J background.
Volume: 21
Issue: 1
Pages: 97-104
Publication  
First Author: Laffaire J
Year: 2009
Journal: BMC Genomics
Title: Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development.
Volume: 10
Pages: 138
Publication
First Author: Suzuki M
Year: 2016
Journal: BMC Genet
Title: Genetic dissection of the fatty liver QTL Fl1sa by using congenic mice and identification of candidate genes in the liver and epididymal fat.
Volume: 17
Issue: 1
Pages: 145
Publication  
First Author: Lu L
Year: 2008
Journal: BMC Genomics
Title: Using gene expression databases for classical trait QTL candidate gene discovery in the BXD recombinant inbred genetic reference population: mouse forebrain weight.
Volume: 9
Pages: 444
Publication
First Author: Simmons EC
Year: 2020
Journal: J Pharmacol Exp Ther
Title: 5-hydroxytryptamine 1F Receptor Agonist Induces Mitochondrial Biogenesis and Promotes Recovery from Spinal Cord Injury.
Volume: 372
Issue: 2
Pages: 216-223
Publication
First Author: Smallwood TL
Year: 2014
Journal: G3 (Bethesda)
Title: High-resolution genetic mapping in the diversity outbred mouse population identifies Apobec1 as a candidate gene for atherosclerosis.
Volume: 4
Issue: 12
Pages: 2353-63
Publication
First Author: Bowne SJ
Year: 2002
Journal: Hum Mol Genet
Title: Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.
Volume: 11
Issue: 5
Pages: 559-68
Publication  
First Author: Iwata T
Year: 2013
Journal: BMC Genomics
Title: Bacillus subtilis genome vector-based complete manipulation and reconstruction of genomic DNA for mouse transgenesis.
Volume: 14
Pages: 300
Publication  
First Author: Lorè NI
Year: 2020
Journal: mBio
Title: Collaborative Cross Mice Yield Genetic Modifiers for Pseudomonas aeruginosa Infection in Human Lung Disease.
Volume: 11
Issue: 2
Publication  
First Author: Stiemke AB
Year: 2020
Journal: Front Genet
Title: Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma.
Volume: 11
Pages: 31
Publication
First Author: Camerino M
Year: 2024
Journal: Epigenetics Chromatin
Title: Analysis of long-range chromatin contacts, compartments and looping between mouse embryonic stem cells, lens epithelium and lens fibers.
Volume: 17
Issue: 1
Pages: 10
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Strain
Attribute String: inbred strain
Publication
First Author: Abraira VE
Year: 2010
Journal: PLoS One
Title: Vertebrate Lrig3-ErbB interactions occur in vitro but are unlikely to play a role in Lrig3-dependent inner ear morphogenesis.
Volume: 5
Issue: 2
Pages: e8981
Publication
First Author: Balthasar N
Year: 2004
Journal: Neuron
Title: Leptin receptor signaling in POMC neurons is required for normal body weight homeostasis.
Volume: 42
Issue: 6
Pages: 983-91
Publication
First Author: Ogórek M
Year: 2017
Journal: Metallomics
Title: Atp7a and Atp7b regulate copper homeostasis in developing male germ cells in mice.
Volume: 9
Issue: 9
Pages: 1288-1303
Publication
First Author: Cocas LA
Year: 2009
Journal: J Neurosci
Title: Emx1-lineage progenitors differentially contribute to neural diversity in the striatum and amygdala.
Volume: 29
Issue: 50
Pages: 15933-46
Publication
First Author: Wong YL
Year: 2019
Journal: Int Immunol
Title: Gp49B is a pathogenic marker for auto-antibody-producing plasma cells in lupus-prone BXSB/Yaa mice.
Volume: 31
Issue: 6
Pages: 397-406
Publication
First Author: Boross P
Year: 2011
Journal: J Immunol
Title: The inhibiting Fc receptor for IgG, FcγRIIB, is a modifier of autoimmune susceptibility.
Volume: 187
Issue: 3
Pages: 1304-13
Publication
First Author: Deane JA
Year: 2007
Journal: Immunity
Title: Control of toll-like receptor 7 expression is essential to restrict autoimmunity and dendritic cell proliferation.
Volume: 27
Issue: 5
Pages: 801-10
Publication
First Author: Kikuchi S
Year: 2006
Journal: J Immunol
Title: Contribution of NZB autoimmunity 2 to Y-linked autoimmune acceleration-induced monocytosis in association with murine systemic lupus.
Volume: 176
Issue: 5
Pages: 3240-7
Publication  
First Author: Pellerin A
Year: 2021
Journal: JCI Insight
Title: Monoallelic IRF5 deficiency in B cells prevents murine lupus.
Volume: 6
Issue: 15
Publication
First Author: Bollée G
Year: 2011
Journal: Nat Med
Title: Epidermal growth factor receptor promotes glomerular injury and renal failure in rapidly progressive crescentic glomerulonephritis.
Volume: 17
Issue: 10
Pages: 1242-50
Publication    
First Author: Okuma H
Year: 2023
Journal: Elife
Title: N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy.
Volume: 12
Publication
First Author: Hövelmeyer N
Year: 2005
Journal: J Immunol
Title: Apoptosis of oligodendrocytes via Fas and TNF-R1 is a key event in the induction of experimental autoimmune encephalomyelitis.
Volume: 175
Issue: 9
Pages: 5875-84
Publication
First Author: Nguyen CDK
Year: 2024
Journal: Cell Rep
Title: PRMT1 promotes epigenetic reprogramming associated with acquired chemoresistance in pancreatic cancer.
Volume: 43
Issue: 5
Pages: 114176
Publication
First Author: Marechal D
Year: 2019
Journal: Hum Mol Genet
Title: Cbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1a.
Volume: 28
Issue: 9
Pages: 1561-1577
Publication
First Author: Lin HV
Year: 2011
Journal: J Biol Chem
Title: Reconstitution of insulin action in muscle, white adipose tissue, and brain of insulin receptor knock-out mice fails to rescue diabetes.
Volume: 286
Issue: 11
Pages: 9797-804
Publication  
First Author: Murano T
Year: 2019
Journal: Commun Biol
Title: Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders.
Volume: 2
Pages: 32
Publication
First Author: Stefater JA 3rd
Year: 2011
Journal: Nature
Title: Regulation of angiogenesis by a non-canonical Wnt-Flt1 pathway in myeloid cells.
Volume: 474
Issue: 7352
Pages: 511-5
Publication
First Author: Inman KE
Year: 2013
Journal: PLoS Genet
Title: Interaction between Foxc1 and Fgf8 during mammalian jaw patterning and in the pathogenesis of syngnathia.
Volume: 9
Issue: 12
Pages: e1003949
Publication
First Author: Plageman TF Jr
Year: 2011
Journal: Dev Biol
Title: Shroom3 and a Pitx2-N-cadherin pathway function cooperatively to generate asymmetric cell shape changes during gut morphogenesis.
Volume: 357
Issue: 1
Pages: 227-34
Publication
First Author: Maezawa Y
Year: 2012
Journal: PLoS One
Title: A new Cre driver mouse line, Tcf21/Pod1-Cre, targets metanephric mesenchyme.
Volume: 7
Issue: 7
Pages: e40547
Publication  
First Author: Colombo S
Year: 2022
Journal: Development
Title: Stabilization of β-catenin promotes melanocyte specification at the expense of the Schwann cell lineage.
Volume: 149
Issue: 2
Publication  
First Author: Duboc V
Year: 2021
Journal: Development
Title: Tbx4 function during hindlimb development reveals a mechanism that explains the origins of proximal limb defects.
Volume: 148
Issue: 19