MouseMine: Keyword Search

Publication

First Author:	Lamia SN
Year:	2024
Journal:	FASEB J
Title:	Overexpression of enhanced yellow fluorescent protein fused with Channelrhodopsin-2 causes contractile dysfunction in skeletal muscle.
Volume:	38
Issue:	22
Pages:	e70185

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Publication

11739413 | J:73256

First Author:	Hsu W
Year:	2001
Journal:	J Cell Biol
Title:	Impaired mammary gland and lymphoid development caused by inducible expression of Axin in transgenic mice.
Volume:	155
Issue:	6
Pages:	1055-64

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Publication

- | J:172267

First Author:	Griffith AJ
Year:	2011
Journal:	MGI Direct Data Submission
Title:	Tet effector and responder transgenes to regulate Slc26a4 expression

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Publication

16352739 | J:106826

First Author:	Zappulla JP
Year:	2005
Journal:	J Exp Med
Title:	Mastocytosis in mice expressing human Kit receptor with the activating Asp816Val mutation.
Volume:	202
Issue:	12
Pages:	1635-41

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Publication

31837519 | J:288233

First Author:	Bisetto S
Year:	2019
Journal:	iScience
Title:	New Insights into the Lactate Shuttle: Role of MCT4 in the Modulation of the Exercise Capacity.
Volume:	22

Pages:	507-518

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Publication

37643861 | J:353889

First Author:	Whitebirch AC
Year:	2023
Journal:	J Neurosci
Title:	Reduced Cholecystokinin-Expressing Interneuron Input Contributes to Disinhibition of the Hippocampal CA2 Region in a Mouse Model of Temporal Lobe Epilepsy.
Volume:	43
Issue:	41
Pages:	6930-6949

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Publication

34992596 | J:360934

First Author:	ElSayed S
Year:	2021
Journal:	Front Immunol
Title:	Recombinant Human Proteoglycan 4 Regulates Phagocytic Activation of Monocytes and Reduces IL-1β Secretion by Urate Crystal Stimulated Gout PBMCs.
Volume:	12

Pages:	771677

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Publication

32561905 | J:296968

First Author:	Park S
Year:	2020
Journal:	Biol Reprod
Title:	CRISPR/Cas9-mediated genome-edited mice reveal 10 testis-enriched genes are dispensable for male fecundity.
Volume:	103
Issue:	2
Pages:	195-204

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Publication

34585727 | J:320661

First Author:	Zhang X
Year:	2021
Journal:	J Cell Sci
Title:	LRRC23 is a conserved component of the radial spoke that is necessary for sperm motility and male fertility in mice.
Volume:	134
Issue:	20

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Publication

10704866 | J:61351

First Author:	Ainscough JF
Year:	2000
Journal:	Mech Dev
Title:	Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb.
Volume:	91
Issue:	1-2
Pages:	365-8

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Publication

19641964 | J:151613

First Author:	Rodriguez MR
Year:	2009
Journal:	Mamm Genome
Title:	A Cmv2 QTL on chromosome X affects MCMV resistance in New Zealand male mice.
Volume:	20
Issue:	7
Pages:	414-23

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Publication

21268010 | J:175428

First Author:	Pizzolla A
Year:	2011
Journal:	Eur J Immunol
Title:	CD68-expressing cells can prime T cells and initiate autoimmune arthritis in the absence of reactive oxygen species.
Volume:	41
Issue:	2
Pages:	403-12

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Publication

17392169 | J:120135

First Author:	Galliciotti G
Year:	2007
Journal:	Am J Pathol
Title:	Accumulation of mutant neuroserpin precedes development of clinical symptoms in familial encephalopathy with neuroserpin inclusion bodies.
Volume:	170
Issue:	4
Pages:	1305-13

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Publication

30745494 | J:277364

First Author:	Tobita T
Year:	2019
Journal:	J Reprod Dev
Title:	Lvrn expression is not critical for mouse placentation.
Volume:	65
Issue:	3
Pages:	239-244

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Publication

26313466 | J:337008

First Author:	López-Luque J
Year:	2016
Journal:	Hepatology
Title:	Dissecting the role of epidermal growth factor receptor catalytic activity during liver regeneration and hepatocarcinogenesis.
Volume:	63
Issue:	2
Pages:	604-19

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Publication

36564444 | J:336504

First Author:	Oura S
Year:	2022
Journal:	Sci Rep
Title:	Proximity-dependent biotin labeling in testicular germ cells identified TESMIN-associated proteins.
Volume:	12
Issue:	1
Pages:	22198

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Publication

32529245 | J:293874

First Author:	Larasati T
Year:	2020
Journal:	Biol Reprod
Title:	Tmprss12 is required for sperm motility and uterotubal junction migration in mice†.
Volume:	103
Issue:	2
Pages:	254-263

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Allele

Prdm9<em2Kpgn> | MGI:6489980

Name:	PR domain containing 9; endonuclease-mediated mutation 2, Kenneth Paigen
Allele Type:	Endonuclease-mediated
Attribute String:	Hypomorph

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Publication

32301969 | J:296963

First Author:	Nozawa K
Year:	2020
Journal:	Biol Reprod
Title:	Knockout of serine-rich single-pass membrane protein 1 (Ssmem1) causes globozoospermia and sterility in male mice†.
Volume:	103
Issue:	2
Pages:	244-253

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Publication

18984673 | J:157971

First Author:	Brockmann GA
Year:	2009
Journal:	Physiol Genomics
Title:	Genetic factors contributing to obesity and body weight can act through mechanisms affecting muscle weight, fat weight, or both.
Volume:	36
Issue:	2
Pages:	114-26

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Publication

27775065 | J:240489

First Author:	Pan Y
Year:	2016
Journal:	Sci Rep
Title:	Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression.
Volume:	6

Pages:	35970

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Publication

33841077 | J:348494

First Author:	Cochard LM
Year:	2021
Journal:	Front Neurosci
Title:	Manipulation of EGFR-Induced Signaling for the Recruitment of Quiescent Neural Stem Cells in the Adult Mouse Forebrain.
Volume:	15

Pages:	621076

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Allele

Tg(Isl1-lacZ)1Blk | MGI:4356530

Name:	transgene insertion 1, Brian L Black
Allele Type:	Transgenic
Attribute String:	Reporter

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Strain

MGI:4820750 | B6.129-Tg(FBN1*C1663R)F2Hcd/J

Attribute String:

congenic, mutant strain, transgenic

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Allele

Gsdmd<em1Gne> | MGI:6259809

Name:	gasdermin D; endonuclease-mediated mutation 1, Genentech
Allele Type:	Endonuclease-mediated
Attribute String:	Null/knockout

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Allele

rd24 | MGI:7643884

Name:	retinal degeneration 24
Allele Type:	Spontaneous
Attribute String:	Not Specified

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Genotype

Symbol:	iec/iec
Background:	involves: HRS/J * Swiss albino
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	di/di
Background:	Not Specified
Zygosity:	hm
Has Mutant Allele:	true

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Publication

17261592 | J:121370

First Author:	Malin D
Year:	2007
Journal:	Mol Cell Biol
Title:	Forkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expression.
Volume:	27
Issue:	7
Pages:	2486-98

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Publication

27425595 | J:239346

First Author:	Milewski D
Year:	2017
Journal:	Oncogene
Title:	FoxF1 and FoxF2 transcription factors synergistically promote rhabdomyosarcoma carcinogenesis by repressing transcription of p21^Cip1 CDK inhibitor.
Volume:	36
Issue:	6
Pages:	850-862

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Publication

28694463 | J:249724

First Author:	Dudeffant C
Year:	2017
Journal:	Sci Rep
Title:	Contrast-enhanced MR microscopy of amyloid plaques in five mouse models of amyloidosis and in human Alzheimer's disease brains.
Volume:	7
Issue:	1
Pages:	4955

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Publication

31213067 | J:277676

First Author:	Findley CA
Year:	2019
Journal:	ASN Neuro
Title:	Amyloid Beta-Related Alterations to Glutamate Signaling Dynamics During Alzheimer's Disease Progression.
Volume:	11

Pages:	1759091419855541

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Publication

26365177 | J:228348

First Author:	Ishii M
Year:	2015
Journal:	Cell Metab
Title:	Metabolic and Non-Cognitive Manifestations of Alzheimer's Disease: The Hypothalamus as Both Culprit and Target of Pathology.
Volume:	22
Issue:	5
Pages:	761-76

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Publication

24305500 | J:286212

First Author:	Reinert J
Year:	2014
Journal:	J Alzheimers Dis
Title:	Aβ38 in the brains of patients with sporadic and familial Alzheimer's disease and transgenic mouse models.
Volume:	39
Issue:	4
Pages:	871-81

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Publication

33287900 | J:313473

First Author:	Bevan RJ
Year:	2020
Journal:	Acta Neuropathol Commun
Title:	Retinal ganglion cell degeneration correlates with hippocampal spine loss in experimental Alzheimer's disease.
Volume:	8
Issue:	1
Pages:	216

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HT Experiment

E-GEOD-23310 | Uncovering Genes and Regulatory Pathways Related to Urinary Albumin Excretion in Mice

Series Id:	GSE23310
Experiment Type:	transcription profiling by array
Study Type:	Baseline
Source:	ArrayExpress

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HT Experiment

E-GEOD-27236 | Gene expression analysis of cardiac left-ventricle tissue from hybrid mice harboring the Scn5a-1798insD/+ mutation

Series Id:	GSE27236
Experiment Type:	transcription profiling by array
Study Type:	WT vs. Mutant
Source:	ArrayExpress

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HT Experiment

E-GEOD-20724 | Genome-wide expression analysis of mouse chromosome 2 in gonadal fat and liver tissues reveals a complex architecture of obesity

Series Id:	GSE20724
Experiment Type:	transcription profiling by array
Study Type:	Baseline
Source:	ArrayExpress

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Publication

32404941 | J:348427

First Author:	Song G
Year:	2020
Journal:	Sci Rep
Title:	Multimodal Coherent Imaging of Retinal Biomarkers of Alzheimer's Disease in a Mouse Model.
Volume:	10
Issue:	1
Pages:	7912

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Publication

35775150 | J:349319

First Author:	Vande Vyver M
Year:	2022
Journal:	Epilepsia
Title:	Higher susceptibility to 6 Hz corneal kindling and lower responsiveness to antiseizure drugs in mouse models of Alzheimer's disease.
Volume:	63
Issue:	10
Pages:	2703-2715

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Publication

38502413 | J:350687

First Author:	Kong Y
Year:	2024
Journal:	Mol Neurobiol
Title:	Relationship Between Reactive Astrocytes, by [(18)F]SMBT-1 Imaging, with Amyloid-Beta, Tau, Glucose Metabolism, and TSPO in Mouse Models of Alzheimer's Disease.

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Publication

32849642 | J:319606

First Author:	Zhao J
Year:	2020
Journal:	Front Immunol
Title:	Administration of Amyloid Precursor Protein Gene Deleted Mouse ESC-Derived Thymic Epithelial Progenitors Attenuates Alzheimer's Pathology.
Volume:	11

Pages:	1781

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Publication

17075880 | J:116645

First Author:	Cota CD
Year:	2006
Journal:	Dev Dyn
Title:	Mice with mutations in Mahogunin ring finger-1 (Mgrn1) exhibit abnormal patterning of the left-right axis.
Volume:	235
Issue:	12
Pages:	3438-47

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Publication

17720281 | J:129981

First Author:	Sun K
Year:	2007
Journal:	Neurobiol Aging
Title:	Mitochondrial dysfunction precedes neurodegeneration in mahogunin (Mgrn1) mutant mice.
Volume:	28
Issue:	12
Pages:	1840-52

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Publication

19703557 | J:164849

First Author:	Jiao J
Year:	2009
Journal:	Biochim Biophys Acta
Title:	Abnormal regulation of TSG101 in mice with spongiform neurodegeneration.
Volume:	1792
Issue:	10
Pages:	1027-35

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Publication

19422019 | J:152824

First Author:	Jiao J
Year:	2009
Journal:	Genesis
Title:	Transgenic analysis of the physiological functions of Mahogunin Ring Finger-1 isoforms.
Volume:	47
Issue:	8
Pages:	524-34

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Publication

23308235 | J:195809

First Author:	Fujikura K
Year:	2013
Journal:	PLoS One
Title:	Kif14 mutation causes severe brain malformation and hypomyelination.
Volume:	8
Issue:	1
Pages:	e53490

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Publication

24931760 | J:215396

First Author:	Yunus J
Year:	2014
Journal:	Neuroscience
Title:	Cytoarchitecture of the olfactory bulb in the laggard mutant mouse.
Volume:	275

Pages:	259-71

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Strain

MGI:3704899 | 129S1.Cg-Mgrn1<md-nc>

Attribute String:

chemically induced mutation, congenic, mutant strain

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Strain

MGI:3704898 | C3.Cg-Mgrn1<md-nc>

Attribute String:

mutant strain, congenic, chemically induced mutation

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Strain

MGI:3578796 | C3H101H-Mgrn1<md-nc>/H

Attribute String:

chemically induced mutation, mutant stock

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Publication

14467628 | J:166121

First Author:	LYON MF
Year:	1962
Journal:	Z Vererbungsl
Title:	A test for mutagenicity of caffeine in mice.
Volume:	93

Pages:	7-13

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Publication

32966817 | J:299749

First Author:	Kong JH
Year:	2020
Journal:	Dev Cell
Title:	A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development.
Volume:	55
Issue:	4
Pages:	432-449.e12

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Publication

31089807 | J:276804

First Author:	Gunn TM
Year:	2019
Journal:	Mamm Genome
Title:	Chronic and age-dependent effects of the spongiform neurodegeneration-associated MGRN1 E3 ubiquitin ligase on mitochondrial homeostasis.
Volume:	30
Issue:	5-6
Pages:	151-165

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Publication

- | J:15072

First Author:	Phillips RJS
Year:	1971
Journal:	Mouse News Lett
Title:	Non-agouti curly (nc)
Volume:	45

Pages:	25

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Publication

23383230 | J:195780

First Author:	Silvius D
Year:	2013
Journal:	PLoS One
Title:	Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease.
Volume:	8
Issue:	1
Pages:	e55575

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Publication

16439706 | J:289761

First Author:	Matsui R
Year:	2006
Journal:	Arterioscler Thromb Vasc Biol
Title:	Glucose-6-phosphate dehydrogenase deficiency decreases vascular superoxide and atherosclerotic lesions in apolipoprotein E(-/-) mice.
Volume:	26
Issue:	4
Pages:	910-6

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Allele

Athsq1<C57BL/6J> | MGI:2155676

Name:	atherosclerosis susceptibility QTL 1; C57BL/6J
Allele Type:	QTL

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Strain

MGI:2165446 | BALB/cBy-Gulo<sfx>/J

Attribute String:

mutant strain, coisogenic, spontaneous mutation

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Publication

11062347 | J:66648

First Author:	Beamer WG
Year:	2000
Journal:	Bone
Title:	Spontaneous fracture (sfx): a mouse genetic model of defective peripubertal bone formation.
Volume:	27
Issue:	5
Pages:	619-26

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Publication

16059632 | J:112377

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

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Publication

31390373 | J:279103

First Author:	Lindsey RC
Year:	2019
Journal:	PLoS One
Title:	Vitamin C effects on 5-hydroxymethylcytosine and gene expression in osteoblasts and chondrocytes: Potential involvement of PHD2.
Volume:	14
Issue:	8
Pages:	e0220653

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Publication

15674730 | J:95128

First Author:	Jiao Y
Year:	2005
Journal:	Mamm Genome
Title:	A deletion causing spontaneous fracture identified from a candidate region of mouse Chromosome 14.
Volume:	16
Issue:	1
Pages:	20-31

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Publication

12420131 | J:79722

First Author:	Phelan SA
Year:	2002
Journal:	Mamm Genome
Title:	Confirmation and high resolution mapping of an atherosclerosis susceptibility gene in mice on Chromosome 1.
Volume:	13
Issue:	10
Pages:	548-53

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Publication

2499515 | J:9832

First Author:	Paigen B
Year:	1989
Journal:	Genetics
Title:	Ath-2, a second gene determining atherosclerosis susceptibility and high density lipoprotein levels in mice.
Volume:	122
Issue:	1
Pages:	163-8

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Allele

Bwt1<HRS/J> | MGI:3707858

Name:	body weight 1; HRS/J
Allele Type:	QTL

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Publication

17186460 | J:122441

First Author:	Gurley KA
Year:	2006
Journal:	Am J Hum Genet
Title:	Biochemical and genetic analysis of ANK in arthritis and bone disease.
Volume:	79
Issue:	6
Pages:	1017-29

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Allele

Athsq3<C3H/HeJ> | MGI:3819396

Name:	atherosclerosis susceptibility QTL 3; C3H/HeJ
Allele Type:	QTL

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Publication

19173005 | J:144832

First Author:	Watanabe T
Year:	2009
Journal:	PLoS One
Title:	Genetic and molecular analysis of wild-derived arrhythmic mice.
Volume:	4
Issue:	1
Pages:	e4301

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Strain

MGI:5910738 | B6.D2(129X1)-Kif14<lag>

Attribute String:

congenic, mutant strain, spontaneous mutation

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Strain

MGI:6146299 | B6.Cg-Kif14<lag>/Rbrc

Attribute String:

mutant strain, coisogenic, spontaneous mutation

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Allele

Athsq3<C57BL/6J> | MGI:5613586

Name:	atherosclerosis susceptibility QTL 3; C57BL/6J

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Genotype

Symbol:	Gulo/Gulo
Background:	BALB/cBy-Gulo/J
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	Pgis1/Pgis1 Pgis2/Pgis2
Background:	involves: BALB/c * DBA/2
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	Pgis1/Pgis1 Pgis2/Pgis2
Background:	involves: BALB/c * DBA/2
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	Lmr16/Lmr16 Lmr18/Lmr18
Background:	involves: BALB/cHeA * STS/A
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	C1qa/C1qa Sle21<129P2/Ola>/? Sle18/Sle18
Background:	involves: 129P2/Ola * 129S/SvEv * C57BL/6
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	Mgrn1/Mgrn1
Background:	C3.Cg-Mgrn1
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	Mgrn1/Mgrn1
Background:	129S1.Cg-Mgrn1
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	Mgrn1/Mgrn1
Background:	involves: 101/H * C3H/HeH
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	Arrh2/Arrh2 Arrh3/Arrh3
Background:	involves: C57BL/6JJcl * M. m. castaneus
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	Kif14/Kif14 Tg(CAG-Kif14)28LTskk/?
Background:	involves: 129X1/SvJ * C57BL/6JJmsSlc * C57BL/6NJcl * DBA/2NJcl
Zygosity:	cx
Has Mutant Allele:	true

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Genotype

Symbol:	Kif14/Kif14
Background:	B6.D2(129X1)-Kif14
Zygosity:	hm
Has Mutant Allele:	true

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Publication

32727580 | J:311717

First Author:	Kumar S
Year:	2020
Journal:	Acta Neuropathol Commun
Title:	Phosphorylated Aβ peptides in human Down syndrome brain and different Alzheimer's-like mouse models.
Volume:	8
Issue:	1
Pages:	118

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Publication

29501742 | J:273677

First Author:	Li H
Year:	2018
Journal:	Biochem Biophys Res Commun
Title:	FTO is involved in Alzheimer's disease by targeting TSC1-mTOR-Tau signaling.
Volume:	498
Issue:	1
Pages:	234-239

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Publication

37409006 | J:346956

First Author:	Weigel TK
Year:	2023
Journal:	Front Aging Neurosci
Title:	Altered circadian behavior and light sensing in mouse models of Alzheimer's disease.
Volume:	15

Pages:	1218193

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Protein

Q8CIN8

Organism:	Mus musculus/domesticus
Length:	75
Fragment?:	true

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Publication

15320781 | -

First Author:	Lee KN
Year:	2004
Journal:	Curr Med Chem Cardiovasc Hematol Agents
Title:	Alpha2-antiplasmin: potential therapeutic roles in fibrin survival and removal.
Volume:	2
Issue:	4
Pages:	303-10

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Protein Domain

IPR041155 | FERM_F1

Type:

Domain

Description:

This is an F1 lobe domain consisting of a ubiquitin like fold found in FERM region of Jak-family tyrosine kinases []. Multidomain JAK molecules interact with receptors through their FERM and SH2-like domains, triggering a series of phosphorylation events, resulting in the activation of their kinase domains []. Overall, the FERM region maintains the typical three-lobed architecture, with an F1 lobe consisting of a ubiquitin-like fold, an F2 lobe consisting of an acyl-CoA binding protein fold, and an F3 lobe consisting of a pleckstrin-homology (PH) fold [].

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Protein Domain

IPR033833 | Alpha2AP_serpin_dom

Type:

Domain

Description:

Alpha2-antiplasmin (alpha2AP; plasmin inhibitor; MEROPS identifier I04.023) is the primary inhibitor of plasmin, a proteinase that digests fibrin, the main component of blood clots. Alpha2-antiplasmin forms an inactive 1:1 stoichiometric complex with plasmin. It also rapidly crosslinks to fibrin during blood clotting by activated coagulation factor XIII, and as a consequence fibrin becomes more resistant to fibrinolysis. Therefore alpha2AP is important in modulating the effectiveness and persistence of fibrin with respect to its susceptibility to digestion and removal by plasmin [, ]. Alpha2-antiplasmin corresponds to clade F2 of the serpin superfamily (MEROPS family I4) [, ].

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Publication

33140451 | J:300416

First Author:	Yu W
Year:	2020
Journal:	Epilepsia
Title:	Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse.
Volume:	61
Issue:	12
Pages:	2847-2856

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Allele

ita | MGI:3716202

Name:	iasi total atrichia
Allele Type:	Spontaneous

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Publication

19580802 | J:152217

First Author:	Kang J
Year:	2009
Journal:	Dev Biol
Title:	Isl1 is a direct transcriptional target of Forkhead transcription factors in second-heart-field-derived mesoderm.
Volume:	334
Issue:	2
Pages:	513-22

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Allele

Gsdmd<em#Gne> | MGI:5882077

Name:	gasdermin D; endonuclease-mediated mutation, Genentech
Allele Type:	Endonuclease-mediated
Attribute String:	Null/knockout

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Publication

32917873 | J:297014

First Author:	Volchuk A
Year:	2020
Journal:	Nat Commun
Title:	Indirect regulation of HMGB1 release by gasdermin D.
Volume:	11
Issue:	1
Pages:	4561

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Publication

37945599 | J:342413

First Author:	Rosli S
Year:	2023
Journal:	Cell Death Dis
Title:	Gasdermin D promotes hyperinflammation and immunopathology during severe influenza A virus infection.
Volume:	14
Issue:	11
Pages:	727

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Publication

32597834 | J:293960

First Author:	Bulek K
Year:	2020
Journal:	J Clin Invest
Title:	Epithelial-derived gasdermin D mediates nonlytic IL-1β release during experimental colitis.
Volume:	130
Issue:	8
Pages:	4218-4234