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Search results 4401 to 4474 out of 4474 for Kl

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Category: Publication
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Type Details Score
Publication
30733286 | J:272888
First Author: Kubli SP
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: AhR controls redox homeostasis and shapes the tumor microenvironment in BRCA1-associated breast cancer.
Volume: 116
Issue: 9
Pages: 3604-3613
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Publication
28589934 | J:264761
 
First Author: Griffin BD
Year: 2017
Journal: Nat Commun
Title: DNA vaccination protects mice against Zika virus-induced damage to the testes.
Volume: 8
Pages: 15743
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Publication
24589777 | J:209629
First Author: Akbay EA
Year: 2014
Journal: Genes Dev
Title: D-2-hydroxyglutarate produced by mutant IDH2 causes cardiomyopathy and neurodegeneration in mice.
Volume: 28
Issue: 5
Pages: 479-90
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Publication
23680150 | J:199122
First Author: Béguelin W
Year: 2013
Journal: Cancer Cell
Title: EZH2 is required for germinal center formation and somatic EZH2 mutations promote lymphoid transformation.
Volume: 23
Issue: 5
Pages: 677-92
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Publication
37729434 | J:343472
First Author: Wu G
Year: 2023
Journal: Sci Transl Med
Title: TP63 fusions drive multicomplex enhancer rewiring, lymphomagenesis, and EZH2 dependence.
Volume: 15
Issue: 714
Pages: eadi7244
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Publication
37117223 | J:340650
First Author: Jami S
Year: 2023
Journal: Nat Commun
Title: Pain-causing stinging nettle toxins target TMEM233 to modulate Na(V)1.7 function.
Volume: 14
Issue: 1
Pages: 2442
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Publication
28424246 | J:243973
First Author: Moffitt AB
Year: 2017
Journal: J Exp Med
Title: Enteropathy-associated T cell lymphoma subtypes are characterized by loss of function of SETD2.
Volume: 214
Issue: 5
Pages: 1371-1386
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Publication
28530678 | J:242757
First Author: Liu X
Year: 2017
Journal: Nat Genet
Title: The complex genetics of hypoplastic left heart syndrome.
Volume: 49
Issue: 7
Pages: 1152-1159
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Publication
35862771 | J:327836
First Author: Schäfer A
Year: 2022
Journal: mBio
Title: A Multitrait Locus Regulates Sarbecovirus Pathogenesis.
Volume: 13
Issue: 4
Pages: e0145422
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Publication
23431148 | J:196079
First Author: Welsbie DS
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Functional genomic screening identifies dual leucine zipper kinase as a key mediator of retinal ganglion cell death.
Volume: 110
Issue: 10
Pages: 4045-50
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Publication
38776389 | J:351125
First Author: Martinez DR
Year: 2024
Journal: Sci Transl Med
Title: The oral nucleoside prodrug GS-5245 is efficacious against SARS-CoV-2 and other endemic, epidemic, and enzootic coronaviruses.
Volume: 16
Issue: 748
Pages: eadj4504
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Publication
37261910 | J:339976
 
First Author: Braun T
Year: 2023
Journal: JCI Insight
Title: Mucosal transcriptomics highlight lncRNAs implicated in ulcerative colitis, Crohn's disease, and celiac disease.
Volume: 8
Issue: 14
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Publication
24487591 | J:209427
First Author: te Vruchte D
Year: 2014
Journal: J Clin Invest
Title: Relative acidic compartment volume as a lysosomal storage disorder-associated biomarker.
Volume: 124
Issue: 3
Pages: 1320-8
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Publication
25679959 | J:224006
First Author: Didion JP
Year: 2015
Journal: PLoS Genet
Title: A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2.
Volume: 11
Issue: 2
Pages: e1004850
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Publication
33545064 | J:305483
First Author: Patton EE
Year: 2021
Journal: Cancer Cell
Title: Melanoma models for the next generation of therapies.
Volume: 39
Issue: 5
Pages: 610-631
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Publication
35256775 | J:355014
First Author: Chen LL
Year: 2022
Journal: Nat Cell Biol
Title: Itaconate inhibits TET DNA dioxygenases to dampen inflammatory responses.
Volume: 24
Issue: 3
Pages: 353-363
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Publication
33828302 | J:325751
First Author: Reinfeld BI
Year: 2021
Journal: Nature
Title: Cell-programmed nutrient partitioning in the tumour microenvironment.
Volume: 593
Issue: 7858
Pages: 282-288
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Publication
37673892 | J:355389
First Author: Antal CE
Year: 2023
Journal: Nat Commun
Title: A super-enhancer-regulated RNA-binding protein cascade drives pancreatic cancer.
Volume: 14
Issue: 1
Pages: 5195
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Publication
38750308 | J:361147
First Author: Chiou S
Year: 2024
Journal: EMBO Mol Med
Title: An immunohistochemical atlas of necroptotic pathway expression.
Volume: 16
Issue: 7
Pages: 1717-1749
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Publication
23040067 | J:356276
First Author: Morán I
Year: 2012
Journal: Cell Metab
Title: Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes.
Volume: 16
Issue: 4
Pages: 435-48
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Publication
36471070 | J:356683
First Author: Jessa S
Year: 2022
Journal: Nat Genet
Title: K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas.
Volume: 54
Issue: 12
Pages: 1865-1880
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Publication
39112630 | J:361626
First Author: Kousa AI
Year: 2024
Journal: Nat Immunol
Title: Age-related epithelial defects limit thymic function and regeneration.
Volume: 25
Issue: 9
Pages: 1593-1606
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Publication
7521281 | J:13166
First Author: Duttlinger R
Year: 1993
Journal: Development
Title: W-sash affects positive and negative elements controlling c-kit expression: ectopic c-kit expression at sites of kit-ligand expression affects melanogenesis.
Volume: 118
Issue: 3
Pages: 705-17
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Publication
7515099 | J:18328
First Author: Yee NS
Year: 1994
Journal: J Exp Med
Title: Role of kit-ligand in proliferation and suppression of apoptosis in mast cells: basis for radiosensitivity of white spotting and steel mutant mice.
Volume: 179
Issue: 6
Pages: 1777-87
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Publication
7519481 | J:18341
   
First Author: Besmer P
Year: 1993
Journal: Dev Suppl
Title: The kit-ligand (steel factor) and its receptor c-kit/W: pleiotropic roles in gametogenesis and melanogenesis.
Pages: 125-37
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Publication
8703029 | J:35441
First Author: Lu-Kuo JM
Year: 1996
Journal: J Biol Chem
Title: Post-transcriptional stabilization by interleukin-1beta of interleukin-6 mRNA induced by c-kit ligand and interleukin-10 in mouse bone marrow-derived mast cells.
Volume: 271
Issue: 36
Pages: 22169-74
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Publication
31217582 | J:279976
First Author: Oz-Levi D
Year: 2019
Journal: Nature
Title: Noncoding deletions reveal a gene that is critical for intestinal function.
Volume: 571
Issue: 7763
Pages: 107-111
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Publication
31827282 | J:284983
First Author: MacPherson L
Year: 2020
Journal: Nature
Title: HBO1 is required for the maintenance of leukaemia stem cells.
Volume: 577
Issue: 7789
Pages: 266-270
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Publication
20835237 | J:175330
First Author: Otto EA
Year: 2010
Journal: Nat Genet
Title: Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.
Volume: 42
Issue: 10
Pages: 840-50
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Publication
37749326 | J:350128
First Author: Yin Z
Year: 2023
Journal: Nat Immunol
Title: APOE4 impairs the microglial response in Alzheimer's disease by inducing TGFβ-mediated checkpoints.
Volume: 24
Issue: 11
Pages: 1839-1853
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Publication
26084801 | J:230613
First Author: Mirabello L
Year: 2015
Journal: Cancer Discov
Title: A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
Volume: 5
Issue: 9
Pages: 920-31
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Publication
37188781 | J:341134
First Author: Lopera F
Year: 2023
Journal: Nat Med
Title: Resilience to autosomal dominant Alzheimer's disease in a Reelin-COLBOS heterozygous man.
Volume: 29
Issue: 5
Pages: 1243-1252
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Publication
30069049 | J:265284
First Author: Baell JB
Year: 2018
Journal: Nature
Title: Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth.
Volume: 560
Issue: 7717
Pages: 253-257
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Publication
35985343 | J:328532
First Author: Shi DD
Year: 2022
Journal: Cancer Cell
Title: De novo pyrimidine synthesis is a targetable vulnerability in IDH mutant glioma.
Volume: 40
Issue: 9
Pages: 939-956.e16
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Publication
29040572 | J:247931
First Author: Peng Y
Year: 2017
Journal: Hum Mol Genet
Title: Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Volume: 26
Issue: 24
Pages: 4937-4950
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Publication
34888534 | J:320813
 
First Author: Teekakirikul P
Year: 2021
Journal: HGG Adv
Title: Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
Volume: 2
Issue: 3
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Publication
10431246 | J:56550
First Author: Nusbaum C
Year: 1999
Journal: Nat Genet
Title: A YAC-based physical map of the mouse genome.
Volume: 22
Issue: 4
Pages: 388-93
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Publication
27158907 | J:239726
First Author: Ishizuka AS
Year: 2016
Journal: Nat Med
Title: Protection against malaria at 1 year and immune correlates following PfSPZ vaccination.
Volume: 22
Issue: 6
Pages: 614-23
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Publication
28528867 | J:242567
First Author: Zhang Y
Year: 2017
Journal: Cancer Cell
Title: A Pan-Cancer Proteogenomic Atlas of PI3K/AKT/mTOR Pathway Alterations.
Volume: 31
Issue: 6
Pages: 820-832.e3
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Publication
28447668 | J:250569
 
First Author: Fang J
Year: 2017
Journal: Nat Commun
Title: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148.
Volume: 8
Pages: 15034
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Publication
28650954 | J:246057
 
First Author: Karp NA
Year: 2017
Journal: Nat Commun
Title: Prevalence of sexual dimorphism in mammalian phenotypic traits.
Volume: 8
Pages: 15475
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Publication
29026089 | J:253587
First Author: Bowl MR
Year: 2017
Journal: Nat Commun
Title: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Volume: 8
Issue: 1
Pages: 886
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Publication
33436573 | J:300887
First Author: Fougeroux C
Year: 2021
Journal: Nat Commun
Title: Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity.
Volume: 12
Issue: 1
Pages: 324
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Publication
33160446 | J:298609
First Author: Walls AC
Year: 2020
Journal: Cell
Title: Elicitation of Potent Neutralizing Antibody Responses by Designed Protein Nanoparticle Vaccines for SARS-CoV-2.
Volume: 183
Issue: 5
Pages: 1367-1382.e17
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Publication
35105861 | J:320238
First Author: Khadka P
Year: 2022
Journal: Nat Commun
Title: PPM1D mutations are oncogenic drivers of de novo diffuse midline glioma formation.
Volume: 13
Issue: 1
Pages: 604
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Publication
38351382 | J:346214
First Author: Malla SB
Year: 2024
Journal: Nat Genet
Title: Pathway level subtyping identifies a slow-cycling biological phenotype associated with poor clinical outcomes in colorectal cancer.
Volume: 56
Issue: 3
Pages: 458-472
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Publication
- | J:14275
 
First Author: Compton JG
Year: 1988
Journal: Mouse News Lett
Title: Keratin genes. Proximity to mutant loci on Chr 11 and Chr 15 that affect the epidermis, and linkage to homeobox homolog genes
Volume: 80
Pages: 165-6
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Publication
- | J:16020
 
First Author: Compton
Year: 1990
Journal: Mouse Genome
Title: Defective development of embryonic ectoderm of velvet coat mice is associated with deletion of type II keratin genes
Volume: 86
Pages: 240
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Publication
31327527 | J:355240
First Author: Neftel C
Year: 2019
Journal: Cell
Title: An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma.
Volume: 178
Issue: 4
Pages: 835-849.e21
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Publication
39603236 | J:360155
First Author: Ogishi M
Year: 2024
Journal: Immunity
Title: Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling.
Volume: 57
Issue: 12
Pages: 2790-2807.e15
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Publication
33259802 | J:299739
First Author: Chen CCL
Year: 2020
Journal: Cell
Title: Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for Gliomagenesis.
Volume: 183
Issue: 6
Pages: 1617-1633.e22
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Publication
37289866 | J:337205
First Author: Singh P
Year: 2023
Journal: Science
Title: Taurine deficiency as a driver of aging.
Volume: 380
Issue: 6649
Pages: eabn9257
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Publication
39419027 | J:358137
First Author: Gong M
Year: 2024
Journal: Am J Hum Genet
Title: MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway.
Volume: 111
Issue: 11
Pages: 2392-2410
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Publication
39137778 | J:353571
First Author: Jia X
Year: 2024
Journal: Cell
Title: High expression of oleoyl-ACP hydrolase underpins life-threatening respiratory viral diseases.
Volume: 187
Issue: 17
Pages: 4586-4604.e20
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Publication
30401457 | J:326484
First Author: Santos-Cortez RLP
Year: 2018
Journal: Am J Hum Genet
Title: FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Volume: 103
Issue: 5
Pages: 679-690
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Publication
26829751 | J:231978
First Author: Bandopadhayay P
Year: 2016
Journal: Nat Genet
Title: MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism.
Volume: 48
Issue: 3
Pages: 273-82
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Publication
28650483 | J:256607
First Author: Meehan TF
Year: 2017
Journal: Nat Genet
Title: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Volume: 49
Issue: 8
Pages: 1231-1238
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Publication
29348434 | J:256608
First Author: Rozman J
Year: 2018
Journal: Nat Commun
Title: Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
Volume: 9
Issue: 1
Pages: 288
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Publication
30588515 | J:267633
 
First Author: Moore BA
Year: 2018
Journal: Commun Biol
Title: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Volume: 1
Pages: 236
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Publication
32756549 | J:297398
First Author: Corbett KS
Year: 2020
Journal: Nature
Title: SARS-CoV-2 mRNA vaccine design enabled by prototype pathogen preparedness.
Volume: 586
Issue: 7830
Pages: 567-571
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Publication
33370286 | J:301500
First Author: Swan AL
Year: 2020
Journal: PLoS Genet
Title: Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
Volume: 16
Issue: 12
Pages: e1009190
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Publication
36201590 | J:330279
First Author: Yanchus C
Year: 2022
Journal: Science
Title: A noncoding single-nucleotide polymorphism at 8q24 drives IDH1-mutant glioma formation.
Volume: 378
Issue: 6615
Pages: 68-78
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Publication
29100089 | J:262321
First Author: Küry S
Year: 2017
Journal: Am J Hum Genet
Title: De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Volume: 101
Issue: 5
Pages: 768-788
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Publication
37845353 | J:342661
First Author: Roychowdhury T
Year: 2023
Journal: Nat Genet
Title: Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target.
Volume: 55
Issue: 11
Pages: 1831-1842
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Publication
27626380 | J:236599
First Author: Dickinson ME
Year: 2016
Journal: Nature
Title: High-throughput discovery of novel developmental phenotypes.
Volume: 537
Issue: 7621
Pages: 508-514
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Publication
21460841 | -
First Author: Naj AC
Year: 2011
Journal: Nat Genet
Title: Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Volume: 43
Issue: 5
Pages: 436-41
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Publication
26760213 | J:241192
First Author: Morrissy AS
Year: 2016
Journal: Nature
Title: Divergent clonal selection dominates medulloblastoma at recurrence.
Volume: 529
Issue: 7586
Pages: 351-7
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Publication
36131014 | J:340417
First Author: Hendrikse LD
Year: 2022
Journal: Nature
Title: Failure of human rhombic lip differentiation underlies medulloblastoma formation.
Volume: 609
Issue: 7929
Pages: 1021-1028
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Publication
- | J:2538
First Author: Weinshilboum RM
Year: 1992
Journal: Mouse Genome
Title: Tpmt and Ly-28: localization of mouse chromosome 13
Volume: 90
Issue: 3
Pages: 446-48
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20686565 | -
First Author: Teslovich TM
Year: 2010
Journal: Nature
Title: Biological, clinical and population relevance of 95 loci for blood lipids.
Volume: 466
Issue: 7307
Pages: 707-13
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22722634 | -
First Author: Allen M
Year: 2012
Journal: Neurology
Title: Novel late-onset Alzheimer disease loci variants associate with brain gene expression.
Volume: 79
Issue: 3
Pages: 221-8
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12040188 | J:77145
First Author: Mural RJ
Year: 2002
Journal: Science
Title: A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome.
Volume: 296
Issue: 5573
Pages: 1661-71
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Publication
26551672 | J:231937
First Author: Gaulton KJ
Year: 2015
Journal: Nat Genet
Title: Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
Volume: 47
Issue: 12
Pages: 1415-25
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Publication
34349265 | J:326210
First Author: Ruth KS
Year: 2021
Journal: Nature
Title: Genetic insights into biological mechanisms governing human ovarian ageing.
Volume: 596
Issue: 7872
Pages: 393-397
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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