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]TissueEyeCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13.Crackower M.A., Heng H.H., Tsui L.C.CategorySequencesSourceMGI: 1306778PubMedEurope PMCGenomics 53:247-248 (1998)Mapped to12
Gene trap expression and mutational analysis for genes involved in the development of the mammalian nervous system.Stoykova A., Chowdhury K., Bonaldo P., Torres M., Gruss P.View abstractCategoriesSequences, ExpressionSourceMGI: 1306778PubMedEurope PMCDev Dyn 212:198-213 (1998)Mapped to29
The mouse and rat MAP1B genes: genomic organization and alternative transcription.Kutschera W., Zauner W., Wiche G., Propst F.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCGenomics 49:430-436 (1998)Mapped to12
A DEAD-family protein gene, Ddx4, encoding a murine homolog of Drosophila vasa maps to the distal end of mouse chromosome 13.Abe K., Noce T.CategorySequencesSourceMGI: 1306778PubMedEurope PMCMamm Genome 8:622-623 (1997)Mapped to13
Delayed development of nervous system in mice homozygous for disrupted microtubule-associated protein 1B (MAP1B) gene.Takei Y., Kondo S., Harada A., Inomata S., Noda T., Hirokawa N.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCJ Cell Biol 137:1615-1626 (1997)Mapped to12
Otp maps to mouse chromosome 13.Wang W., Lufkin T.CategorySequencesSourceMGI: 1306778PubMedEurope PMCMamm Genome 8:537-538 (1997)Mapped to11
High-resolution linkage map of mouse chromosome 13 in the vicinity of the host resistance locus Lgn1.Beckers M.C., Ernst E., Diez E., Morissette C., Gervais F., Hunter K., Housman D., Yoshida S., Skamene E., Gros P.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCGenomics 39:254-263 (1997)Mapped to34
Evidence for the stochastic integration of gene trap vectors into the mouse germline.Chowdhury K., Bonaldo P., Torres M., Stoykova A., Gruss P.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCNucleic Acids Res 25:1531-1536 (1997)Mapped to16
The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5.Scharf J.M., Damron D., Frisella A., Bruno S., Beggs A.H., Kunkel L.M., Dietrich W.F.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCGenomics 38:405-417 (1996)Cited in33Mapped to50
An integrated genetic map of the pearl locus of mouse chromosome 13.Seymour A.B., Yanak B.L., O'Brien E.P., Rusiniak M.E., Novak E.K., Pinto L.H., Swank R.T., Gorin M.B.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCGenome Res 6:538-544 (1996)Mapped to99+
Isolation and sequencing of the 5' end of the rat microtubule-associated protein (MAP1B)-encoding cDNA.Liu D., Fischer I.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCGene 171:307-308 (1996)Cited in1Mapped to10
Differential expression of N-CAM, vimentin and MAP1B during initial pathfinding of olfactory receptor neurons in the mouse embryo.Aoki K., Osumi-Yamashita N., Ninomiya Y., Eto K.View abstractCategoryExpressionSourceMGI: 1306778PubMedEurope PMCAnat Embryol (Berl) 192:211-220 (1995)Mapped to36
Neuronal abnormalities in microtubule-associated protein 1B mutant mice.Edelmann W., Zervas M., Costello P., Roback L., Fischer I., Hammarback J.A., Cowan N., Davies P., Wainer B., Kucherlapati R.View abstractCategoryPhenotypes & VariantsSourceMGI: 1306778PubMedEurope PMCProc Natl Acad Sci U S A 93:1270-1275 (1996)Mapped to12
Chromosome assignment of human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels.Durkin A.S., Nierman W.C., Zoghbi H., Jones C., Kozak C.A., Maglott D.R.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCCytogenet Cell Genet 65:86-91 (1994)Mapped to10
Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD).O'Brien E.P., Novak E.K., Zhen L., Manly K.F., Stephenson D., Swank R.T.View abstractCategorySequencesSourceMGI: 1306778PubMedEurope PMCMamm Genome 6:19-24 (1995)Mapped to28
FMRP regulates postnatal neuronal migration via MAP1B.Messaoudi S., Allam A., Stoufflet J., Paillard T., Le Ven A., Fouquet C., Doulazmi M., Trembleau A., Caille I.View abstractAnnotationFMRP regulates postnatal neuronal migration via MAP1B.CategoryFunctionSourceGeneRif: 17755PubMedEurope PMCElife 12:RP88782-RP88782 (2024)Mapped to18
Docking protein 6 (DOK6) selectively docks the neurotrophic signaling transduction to restrain peripheral neuropathy.Guo Y., Xiang P., Sun X., Liu W., Zhou J., Yin B., Hou L., Qiang B., Li H.[...], Peng X.View abstractCategoryFunctionSourceMGI: 1306778PubMedEurope PMCSignal Transduct Target Ther 9:32-32 (2024)Mapped to99+
The role of Map1b in regulating osteoblast polarity, proliferation, differentiation and migration.Peng L., Zhang D., Tu H., Wu D., Xiang S., Yang W., Zhao Y., Yang J.View abstractAnnotationThe role of Map1b in regulating osteoblast polarity proliferation differentiation and migration.CategoryFunctionSourceGeneRif: 17755PubMedEurope PMCBone 181:117038-117038 (2024)Mapped to9
Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.Salamon I., Park Y., Miskic T., Kopic J., Matteson P., Page N.F., Roque A., McAuliffe G.W., Favate J.[...], Rasin M.R.View abstractCategoryFunctionSourceMGI: 1306778PubMedEurope PMCNat Commun 14:6025-6025 (2023)Mapped to99+
Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway.Guo Y., Shen M., Dong Q., Mendez-Albelo N.M., Huang S.X., Sirois C.L., Le J., Li M., Jarzembowski E.D.[...], Doherty D.View abstractSourceMGI: 1306778PubMedEurope PMCNat Commun 14:3801-3801 (2023)Mapped to33
NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome.Kurosaki T., Sakano H., Proschel C., Wheeler J., Hewko A., Maquat L.E.View abstractCategoryFunctionSourceMGI: 1306778PubMedEurope PMCGenome Biol 22:317-317 (2021)Mapped to63
Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy.Bora G., Hensel N., Rademacher S., Koyunoglu D., Sunguroglu M., Aksu-Menges E., Balcı-Hayta B., Claus P., Erdem-Yurter H.View abstractAnnotationMicrotubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy.CategoryFunctionSourceGeneRif: 17755PubMedEurope PMCHum Mol Genet 29:3935-3944 (2021)Mapped to18
FMRP-absence-induced up-regulation of hypothalamic MAP1B expression decreases AgRP level linking with reduces in food intake and body weight.Long J.Y., Jiang W., Xia H.B., Fu J.Y., Lu P., Hu F., Feng W.C., Sun W.W., Gao M.M.[...], Long Y.S.View abstractAnnotationFMRP-absence-induced up-regulation of hypothalamic MAP1B expression decreases AgRP level linking with reduces in food intake and body weight.CategoryFunctionSourceGeneRif: 17755, MGI: 1306778PubMedEurope PMCNeurochem Int 140:104847-104847 (2020)Mapped to27
Caspr2 interacts with type 1 inositol 1,4,5-trisphosphate receptor in the developing cerebellum and regulates Purkinje cell morphology.Argent L., Winter F., Prickett I., Carrasquero-Ordaz M., Olsen A.L., Kramer H., Lancaster E., Becker E.B.E.View abstractCategoryFunctionSourceMGI: 1306778PubMedEurope PMCJ Biol Chem 295:12716-12726 (2020)Mapped to76