The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]StrainFVB/NTissueMammary tumor. C3CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Basal lamina molecules are concentrated in myogenic regions of the mouse limb bud.Godfrey E.W., Gradall K.S.View abstractCategoriesSequences, Expression, Subcellular LocationSourceMGI: 88456PubMedEurope PMCAnat Embryol (Berl) 198:481-486 (1998)Mapped to75
Sensory ataxia and muscle spindle agenesis in mice lacking the transcription factor Egr3.Tourtellotte W.G., Milbrandt J.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCNat. Genet. 20:87-91 (1998)Cited in1Mapped to54
Distribution of fibronectin, type I collagen, type IV collagen, and laminin in the cardiac jelly of the mouse embryonic heart with retinoic acid-induced complete transposition of the great arteries.Nakajima Y., Morishima M., Nakazawa M., Momma K., Nakamura H.View abstractCategoriesSequences, ExpressionSourceMGI: 88456PubMedEurope PMCAnat Rec 249:478-485 (1997)Mapped to60
Localization of basement membrane-associated protein isoforms during development of the ocular surface of mouse eye.Qin P., Piechocki M., Lu S., Kurpakus M.A.View abstractCategoriesSequences, ExpressionSourceMGI: 88456PubMedEurope PMCDev Dyn 209:367-376 (1997)Mapped to67
Transcription factor Sp1 is essential for early embryonic development but dispensable for cell growth and differentiation.Marin M., Karis A., Visser P., Grosveld F., Philipsen S.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCCell 89:619-628 (1997)Mapped to65
Muscle progenitor cells failing to respond to positional cues adopt non- myogenic fates in myf-5 null mice.Tajbakhsh S., Rocancourt D., Buckingham M.View abstractCategoriesFunction, ExpressionSourceMGI: 88456PubMedEurope PMCNature 384:266-270 (1996)Mapped to54
Developmental changes in seminiferous tubule extracellular matrix components of the mouse testis: alpha 3(IV) collagen chain expressed at the initiation of spermatogenesis.Enders G.C., Kahsai T.Z., Lian G., Funabiki K., Killen P.D., Hudson B.G.View abstractCategoriesSequences, ExpressionSourceMGI: 88456PubMedEurope PMCBiol Reprod 53:1489-1499 (1995)Mapped to42
Encyclopedia of the mouse genome III. October 1993. Mouse X chromosome.Brown S.D., Avner P., Boyd Y., Chapman V., Rastan S., Sefton L., Thomas J.D., Herman G.E.CategorySequencesSourceMGI: 88456PubMedEurope PMCMamm Genome 4 Spec No:S269-81 (1993)Mapped to13
Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches.Miner J.H., Sanes J.R.View abstractCategorySequencesSourceMGI: 88456PubMedEurope PMCJ. Cell Biol. 127:879-891 (1994)Cited in21Mapped to11
Aberrant differentiation of neuromuscular junctions in mice lacking s- laminin/laminin beta 2.Noakes P.G., Gautam M., Mudd J., Sanes J.R., Merlie J.P.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCNature 374:258-262 (1995)Cited in1Mapped to18
Complex patterns of expression suggest extensive roles for the alpha 2 beta 1 integrin in murine development.Wu J.E., Santoro S.A.View abstractCategorySequencesSourceMGI: 88456PubMedEurope PMCDev. Dyn. 199:292-314 (1994)Cited in1Mapped to28
Genetic determinants of micronucleus formation in vivo.Adams D.J., Barlas B., McIntyre R.E., Salguero I., van der Weyden L., Barros A., Vicente J.R., Karimpour N., Haider A.[...], White J.K.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy.Aypek H., Krisp C., Lu S., Liu S., Kylies D., Kretz O., Wu G., Moritz M., Amann K.[...], Grahammer F.View abstractCategoriesFunction, ExpressionSourceMGI: 88456PubMedEurope PMCJ Clin Invest 132:e147253-e147253 (2022)Mapped to46
NanoLuc reporters identify <i>COL4A5</i> nonsense mutations susceptible to drug-induced stop codon readthrough.Omachi K., Kai H., Roberge M., Miner J.H.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCiScience 25:103891-103891 (2022)Mapped to8
Intravital imaging reveals glomerular capillary distension and endothelial and immune cell activation early in Alport syndrome.Gyarmati G., Shroff U.N., Izuhara A., Hou X., Da Sacco S., Sedrakyan S., Lemley K.V., Amann K., Perin L., Peti-Peterdi J.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 88456PubMedEurope PMCJCI Insight 7:e152676-e152676 (2022)Mapped to8
Identification of an Altered Matrix Signature in Kidney Aging and Disease.Randles M.J., Lausecker F., Kong Q., Suleiman H., Reid G., Kolatsi-Joannou M., Davenport B., Tian P., Falcone S.[...], Lennon R.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCJ Am Soc Nephrol 32:1713-1732 (2021)Mapped to16
FGF8 and BMP2 mediated dynamic regulation of dental mesenchyme proliferation and differentiation via Lhx8/Suv39h1 complex.Zhou C., Chen D., Ren J., Huang D., Li R., Luo H., Guan C., Cao Y., Wang W.View abstractCategoriesFunction, ExpressionSourceMGI: 88456PubMedEurope PMCJ Cell Mol Med 25:3051-3062 (2021)Mapped to99+
Bidirectional, non-necrotizing glomerular crescents are the critical pathology in X-linked Alport syndrome mouse model harboring nonsense mutation of human COL4A5.Song J.Y., Saga N., Kawanishi K., Hashikami K., Takeyama M., Nagata M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 88456PubMedEurope PMCSci Rep 10:18891-18891 (2020)Mapped to8
Glomerular endothelial cell heterogeneity in Alport syndrome.Soloyan H., Thornton M., Villani V., Khatchadourian P., Cravedi P., Angeletti A., Grubbs B., De Filippo R., Perin L., Sedrakyan S.View abstractCategoryFunctionSourceMGI: 88456PubMedEurope PMCSci Rep 10:11414-11414 (2020)Mapped to8
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.Yamamura T., Horinouchi T., Adachi T., Terakawa M., Takaoka Y., Omachi K., Takasato M., Takaishi K., Shoji T.[...], Nozu K.View abstractAnnotationDevelopment of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.CategoryPhenotypes & VariantsSourceGeneRif: 12830, MGI: 88456PubMedEurope PMCNat Commun 11:2777-2777 (2020)Mapped to9
Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background.Falcone S., Wisby L., Nicol T., Blease A., Starbuck B., Parker A., Sanderson J., Brown S.D.M., Scudamore C.L.[...], Potter P.K.View abstractCategoryPhenotypes & VariantsSourceMGI: 88456PubMedEurope PMCSci Rep 9:20398-20398 (2019)Mapped to11
Establishment of X-linked Alport syndrome model mice with a <i>Col4a5</i> R471X mutation.Hashikami K., Asahina M., Nozu K., Iijima K., Nagata M., Takeyama M.View abstractCategoryPhenotypes & VariantsSourceMGI: 88456PubMedEurope PMCBiochem Biophys Rep 17:81-86 (2019)Mapped to8
Type IV collagen alpha6 chain is a regulator of keratin 10 in keratinization of oral mucosal epithelium.Komori T., Ono M., Hara E.S., Ueda J., Nguyen H.T.T., Nguyen H.T., Yonezawa T., Maeba T., Kimura-Ono A.[...], Oohashi T.View abstractCategoriesFunction, ExpressionSourceMGI: 88456PubMedEurope PMCSci Rep 8:2612-2612 (2018)Mapped to42
Pathogenicity of a Human Laminin pii>betapi/i>2 Mutation Revealed in Models of Alport Syndrome.Funk S.D., Bayer R.H., Malone A.F., McKee K.K., Yurchenco P.D., Miner J.H.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 88456PubMedEurope PMCJ Am Soc Nephrol 29:949-960 (2018)Mapped to16