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    Ret ret proto-oncogene [ Mus musculus (house mouse) ]

    Gene ID: 19713, updated on 21-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    RET Signaling Persists in the Adult Intestine and Stimulates Motility by Limiting PYY Release From Enteroendocrine Cells.

    RET Signaling Persists in the Adult Intestine and Stimulates Motility by Limiting PYY Release From Enteroendocrine Cells.
    Shepherd A, Feinstein L, Sabel S, Rastelli D, Mezhibovsky E, Matthews L, Muppirala A, Robinson A, Sharma KR, ElSeht A, Zeve D, Breault DT, Gershon MD, Rao M.,

    02/26/2024
    Ret deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development.

    Ret deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development.
    Vincent E, Chatterjee S, Cannon GH, Auer D, Ross H, Chakravarti A, Goff LA., Free PMC Article

    08/19/2023
    ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse Model.

    ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse Model.
    Zhao Z, Dai X, Jiang G, Lin F.,

    06/13/2023
    A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism.

    A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism.
    Sunardi M, Ito K, Sato Y, Uesaka T, Iwasaki M, Enomoto H., Free PMC Article

    05/30/2023
    The kinase PLK1 promotes the development of Kras/Tp53-mutant lung adenocarcinoma through transcriptional activation of the receptor RET.

    The kinase PLK1 promotes the development of Kras/Tp53-mutant lung adenocarcinoma through transcriptional activation of the receptor RET.
    Kong Y, Allison DB, Zhang Q, He D, Li Y, Mao F, Li C, Li Z, Zhang Y, Wang J, Wang C, Brainson CF, Liu X., Free PMC Article

    10/8/2022
    Bimodal regulation of axonal transport by the GDNF-RET signalling axis in healthy and diseased motor neurons.

    Bimodal regulation of axonal transport by the GDNF-RET signalling axis in healthy and diseased motor neurons.
    Rhymes ER, Tosolini AP, Fellows AD, Mahy W, McDonald NQ, Schiavo G., Free PMC Article

    07/16/2022
    GIPC2 is an endocrine-specific tumor suppressor gene for both sporadic and hereditary tumors of RET- and SDHB-, but not VHL-associated clusters of pheochromocytoma/paraganglioma.

    GIPC2 is an endocrine-specific tumor suppressor gene for both sporadic and hereditary tumors of RET- and SDHB-, but not VHL-associated clusters of pheochromocytoma/paraganglioma.
    Dong Y, Huang Y, Fan C, Wang L, Zhang R, Li W, Guo Z, Wang D, Zheng Z., Free PMC Article

    10/16/2021
    Loss-of-function mutation of c-Ret causes cerebellar hypoplasia in mice with Hirschsprung disease and Down's syndrome.

    Loss-of-function mutation of c-Ret causes cerebellar hypoplasia in mice with Hirschsprung disease and Down's syndrome.
    Ohgami N, Iizuka A, Hirai H, Yajima I, Iida M, Shimada A, Tsuzuki T, Jijiwa M, Asai N, Takahashi M, Kato M., Free PMC Article

    09/11/2021
    Hair graying with aging in mice carrying oncogenic RET.

    Hair graying with aging in mice carrying oncogenic RET.
    Iida M, Tazaki A, Yajima I, Ohgami N, Taguchi N, Goto Y, Kumasaka MY, Prévost-Blondel A, Kono M, Akiyama M, Takahashi M, Kato M., Free PMC Article

    08/28/2021
    RET overactivation leads to concurrent Hirschsprung disease and intestinal ganglioneuromas.

    RET overactivation leads to concurrent Hirschsprung disease and intestinal ganglioneuromas.
    Nagy N, Guyer RA, Hotta R, Zhang D, Newgreen DF, Halasy V, Kovacs T, Goldstein AM., Free PMC Article

    12/26/2020
    Point mutagenesis in mouse reveals contrasting pathogenetic effects between MEN2B- and Hirschsprung disease-associated missense mutations of the RET gene.

    Point mutagenesis in mouse reveals contrasting pathogenetic effects between MEN2B- and Hirschsprung disease-associated missense mutations of the RET gene.
    Nakatani T, Iwasaki M, Yamamichi A, Yoshioka Y, Uesaka T, Bitoh Y, Maeda K, Fukumoto T, Takemoto T, Enomoto H.

    12/12/2020
    Acute stress disrupts intestinal homeostasis via GDNF-RET.

    Acute stress disrupts intestinal homeostasis via GDNF-RET.
    Lin L, Feng B, Zhou R, Liu Y, Li L, Wang K, Yu Y, Liu C, Long X, Gu X, Li B, Wang X, Yang X, Cong Y, Zuo X, Li Y., Free PMC Article

    10/31/2020
    RET can be an essential co-driver of pancreatic tumorigenesis in conjugation with KRAS activity.

    RET, a targetable driver of pancreatic adenocarcinoma.
    Amit M, Na'ara S, Fridman E, Vladovski E, Wasserman T, Milman N, Gil Z.

    10/12/2019
    Removal of Ret disrupts nerve growth factor-mediated TrkA ubiquitination, leading to increased cell surface levels of TrkA, thereby potentiating survival signaling. Ret deletion significantly impairs p75 regulated intramembrane proteolysis cleavage, leading to reduced activation of downstream apoptotic effectors.

    Non-canonical Ret signaling augments p75-mediated cell death in developing sympathetic neurons.
    Donnelly CR, Gabreski NA, Suh EB, Chowdhury M, Pierchala BA., Free PMC Article

    09/21/2019
    Immunohistochemistry and random sparse recombination coupled with histochemical AP staining provided an in-depth characterization of retinal ganglion cells (RGCs), horizontal cells (HCs) and amacrine cells (ACs) expressing RET. Ret is expressed in at least three distinct types of ACs, and ten types of RGCs. Ret expression overlaps with Brn3a in 4 RGC types, with Brn3b in 5 RGC types, and with Brn3c in one RGC type.

    Characterization of retinal ganglion cell, horizontal cell, and amacrine cell types expressing the neurotrophic receptor tyrosine kinase Ret.
    Parmhans N, Sajgo S, Niu J, Luo W, Badea TC., Free PMC Article

    03/16/2019
    An oncogenic role of non-mutated Ret in the mammary gland.

    Chronic expression of wild-type Ret receptor in the mammary gland induces luminal tumors that are sensitive to Ret inhibition.
    Gattelli A, García Solá ME, Roloff TC, Cardiff RD, Kordon EC, Chodosh LA, Hynes NE.

    03/2/2019
    p75 is required for the development of the nonpeptidergic nociceptor lineage by fine-tuning Ret-mediated trophic support.

    p75 Is Required for the Establishment of Postnatal Sensory Neuron Diversity by Potentiating Ret Signaling.
    Chen Z, Donnelly CR, Dominguez B, Harada Y, Lin W, Halim AS, Bengoechea TG, Pierchala BA, Lee KF., Free PMC Article

    06/16/2018
    7-DHC efficiently supports Ret signaling in vitro.

    7-dehydrocholesterol efficiently supports Ret signaling in a mouse model of Smith-Opitz-Lemli syndrome.
    Gou-Fàbregas M, Macià A, Anerillas C, Vaquero M, Jové M, Jain S, Ribera J, Encinas M., Free PMC Article

    05/12/2018
    Results showed that Mn-mediated age-related hearing loss involved a decreased expression and phosphorylation levels of c-Ret in spiral ganglion neurons.

    Manganese-mediated acceleration of age-related hearing loss in mice.
    Ohgami N, Yajima I, Iida M, Li X, Oshino R, Kumasaka MY, Kato M., Free PMC Article

    05/12/2018
    Compromised Survival of Cerebellar Molecular Layer Interneurons Lacking GDNF Receptors GFRalpha1 or RET Impairs Normal Cerebellar Motor Learning

    Compromised Survival of Cerebellar Molecular Layer Interneurons Lacking GDNF Receptors GFRα1 or RET Impairs Normal Cerebellar Motor Learning.
    Sergaki MC, López-Ramos JC, Stagkourakis S, Gruart A, Broberger C, Delgado-García JM, Ibáñez CF., Free PMC Article

    03/10/2018
    Data show that NEDL2 regulates GDNF/Ret/Akt pathway depends on its Nedd8 ligase activity rather than ubiquitin ligase activity.

    NEDL2 regulates enteric nervous system and kidney development in its Nedd8 ligase activity-dependent manner.
    Qiu X, Wei R, Li Y, Zhu Q, Xiong C, Chen Y, Zhang Y, Lu K, He F, Zhang L., Free PMC Article

    12/30/2017
    The cardiac GFRA2 signaling pathway is distinct from the canonical pathway dependent on the RET tyrosine kinase.

    GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway.
    Ishida H, Saba R, Kokkinopoulos I, Hashimoto M, Yamaguchi O, Nowotschin S, Shiraishi M, Ruchaya P, Miller D, Harmer S, Poliandri A, Kogaki S, Sakata Y, Dunkel L, Tinker A, Hadjantonakis AK, Sawa Y, Sasaki H, Ozono K, Suzuki K, Yashiro K., Free PMC Article

    11/25/2017
    Ret is essential to mediate GDNF's neuroprotective and neuroregenerative effect in a Parkinson disease mouse model.

    Ret is essential to mediate GDNF's neuroprotective and neuroregenerative effect in a Parkinson disease mouse model.
    Drinkut A, Tillack K, Meka DP, Schulz JB, Kügler S, Kramer ER., Free PMC Article

    10/28/2017
    Mechanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, modulated by Src and Fak kinases.

    Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia.
    Perea D, Guiu J, Hudry B, Konstantinidou C, Milona A, Hadjieconomou D, Carroll T, Hoyer N, Natarajan D, Kallijärvi J, Walker JA, Soba P, Thapar N, Burns AJ, Jensen KB, Miguel-Aliaga I., Free PMC Article

    10/21/2017
    Authors did not find evidence for genetic interaction between Ret and Sema3d affecting survival, presence of myenteric plexus or intestine transcriptome.

    Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development.
    Kapoor A, Auer DR, Lee D, Chatterjee S, Chakravarti A., Free PMC Article

    10/14/2017
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