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1 Hankeova S, Van Hul N, Laznovsky J, Verboven E, Mangold K, Hensens N, Adori C, Verhoef E, Zikmund T, Dawit F, Kavkova M, Salplachta J, Sjöqvist M, Johansson BR, Hassan MG, Fredriksson L, Baumgärtel K, Bryja V, Lendahl U, Jheon A, Alten F, Fahnehjelm KT, Fischler B, Kaiser J, Andersson ER. Sex differences and risk factors for bleeding in Alagille syndrome. EMBO Mol Med 2022. [DOI: 10.15252/emmm.202215809] [Reference Citation Analysis]
2 Kim E, Kim JY, Kim S, Hong N, Choi S, Park MG, Jang J, Ham SW, Seo S, Lee SY, Lee K, Jeong HJ, Kim SJ, Jeong S, Min K, Kim S, Jin X, Kim SH, Kim S, Kim H. The oncogenic JAG1 intracellular domain is a transcriptional cofactor that acts in concert with DDX17/SMAD3/TGIF2. Cell Reports 2022;41:111626. [DOI: 10.1016/j.celrep.2022.111626] [Reference Citation Analysis]
3 Mašek J, Filipovic I, Hankeová S, He J, Van Hul N, Belicová L, Jiroušková M, Frontino AM, Turetti F, Oliveira DV, Červenka I, Sarnová L, Verboven E, Brabec T, Björkström NK, Gregor M, Dobeš J, Andersson ER. Protection from liver cancer in a mouse model of Alagille syndrome follows dysregulated differentiation of thymocytes and hepatocytes.. [DOI: 10.1101/2022.10.24.513578] [Reference Citation Analysis]
4 Gagliani EK, Gutzwiller LM, Kuang Y, Odaka Y, Hoffmeister P, Hauff S, Turkiewicz A, Harding-theobald E, Dolph PJ, Borggrefe T, Oswald F, Gebelein B, Kovall RA. A Drosophila Su(H) model of Adams-Oliver Syndrome reveals cofactor titration as a mechanism underlying developmental defects. PLoS Genet 2022;18:e1010335. [DOI: 10.1371/journal.pgen.1010335] [Reference Citation Analysis]
5 Dąbrowska J, Biedziak B, Szponar-Żurowska A, Budner M, Jagodziński PP, Płoski R, Mostowska A. Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Mol Genet Genomics 2022. [PMID: 35778651 DOI: 10.1007/s00438-022-01919-w] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Chen D, Forghany Z, Liu X, Wang H, Merks RM, Baker DA. A new model of Notch signaling: Control of Notch receptor cis-inhibition via Notch ligand dimers.. [DOI: 10.1101/2022.05.09.491117] [Reference Citation Analysis]
7 Zhang B, He P, Lawrence JE, Wang S, Tuck E, Williams B, Roberts K, Kleshchevnikov V, Mamanova L, Bolt L, Polanski K, Elmentaite R, Fasouli ES, Prete M, He X, Yayon N, Fu Y, Yang H, Liang C, Zhang H, Fitzpatrick DR, Firth H, Dean A, Barker RA, Storer MA, Wold BJ, Zhang H, Teichmann SA. A human embryonic limb cell atlas resolved in space and time.. [DOI: 10.1101/2022.04.27.489800] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Burton KA, Mahen E, Konnick EQ, Blau S, Dorschner MO, Ramirez AB, Schmechel SC, Song C, Parulkar R, Parker S, Senecal FM, Pritchard CC, Mecham BH, Szeto C, Spilman P, Zhu J, Gadi VK, Ronen R, Stilwell J, Kaldjian E, Dutkowski J, Benz SC, Rabizadeh S, Soon-Shiong P, Blau CA. Safety, Feasibility, and Merits of Longitudinal Molecular Testing of Multiple Metastatic Sites to Inform mTNBC Patient Treatment in the Intensive Trial of Omics in Cancer. JCO Precis Oncol 2022;6:e2100280. [PMID: 35294224 DOI: 10.1200/PO.21.00280] [Reference Citation Analysis]
9 Tan EC, Lai AHM, Brett MSY. Novel phenotypic feature in a patient with a recurrent NOTCH2 nonsense mutation. Am J Med Genet A 2022. [PMID: 35289498 DOI: 10.1002/ajmg.a.62724] [Reference Citation Analysis]
10 Cerrizuela S, Vega-Lopez GA, Méndez-Maldonado K, Velasco I, Aybar MJ. The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies. WIREs Mech Dis 2022;14:e1537. [PMID: 35023327 DOI: 10.1002/wsbm.1537] [Reference Citation Analysis]
11 Yan X, Shang J, Wang R, Wang F, Zhang J. Mechanisms regulating cerebral hypoperfusion in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Biomed Res 2022;36:353. [DOI: 10.7555/jbr.36.20220208] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Wang R, Zhang J, Shang J, Wang F, Yan X. Effects of different regional cerebral blood flow on white matter hyperintensity in CADASIL patients. J Biomed Res 2022;36:368. [DOI: 10.7555/jbr.36.20220006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Braune E, Del Gaudio F, Lendahl U. The Notch Signaling Pathway. Reference Module in Life Sciences 2022. [DOI: 10.1016/b978-0-12-821618-7.00165-6] [Reference Citation Analysis]
14 Yang S, Salazar JL, Li-kroeger D, Yamamoto S. Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila. Methods in Molecular Biology 2022. [DOI: 10.1007/978-1-0716-2201-8_19] [Reference Citation Analysis]
15 Bott LC, Forouhan M, Lieto M, Sala AJ, Ellerington R, Johnson JO, Speciale AA, Criscuolo C, Filla A, Chitayat D, Alkhunaizi E, Shannon P, Nemeth AH, Angelucci F, Lim WF, Striano P, Zara F, Helbig I, Muona M, Courage C, Lehesjoki AE, Berkovic SF, Fischbeck KH, Brancati F, Morimoto RI, Wood MJA, Rinaldi C; Italian Undiagnosed Diseases Network ., ATPase Consortium . Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy. Brain Commun 2021;3:fcab245. [PMID: 34909687 DOI: 10.1093/braincomms/fcab245] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Nur Villar-Quiles R, Romero NB, Tanya S. [JAG2-related muscular dystrophy: When differential diagnosis matters]. Med Sci (Paris) 2021;37 Hors série n° 1:40-3. [PMID: 34878394 DOI: 10.1051/medsci/2021191] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Mukhopadhyay P, Smolenkova I, Seelan RS, Pisano MM, Greene RM. Spatiotemporal Expression and Functional Analysis of miRNA-22 in the Developing Secondary Palate. Cleft Palate Craniofac J 2021;:10556656211054004. [PMID: 34730446 DOI: 10.1177/10556656211054004] [Reference Citation Analysis]
18 Sun L, Zhang J, Su N, Zhang S, Yan F, Lin X, Yu J, Li W, Li X, Xiao S. Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing. Front Aging Neurosci 2021;13:745407. [PMID: 34720994 DOI: 10.3389/fnagi.2021.745407] [Reference Citation Analysis]
19 Saleh S, Ullah M, Naveed H. Cell fate determination is influenced by Notch heterogeneity. 2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC) 2021. [DOI: 10.1109/embc46164.2021.9629491] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Zhdanovskaya N, Firrincieli M, Lazzari S, Pace E, Scribani Rossi P, Felli MP, Talora C, Screpanti I, Palermo R. Targeting Notch to Maximize Chemotherapeutic Benefits: Rationale, Advanced Strategies, and Future Perspectives. Cancers (Basel) 2021;13:5106. [PMID: 34680255 DOI: 10.3390/cancers13205106] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
21 Gagliani EK, Gutzwiller LM, Kuang Y, Odaka Y, Hoffmeister P, Hauff S, Turkiewicz A, Harding-theobald E, Dolph PJ, Borggrefe T, Oswald F, Gebelein B, Kovall RA. A Drosophila Su(H) Model of Adams-Oliver Syndrome Reveals Notch Cofactor Titration as a Mechanism Underlying Developmental Defects.. [DOI: 10.1101/2021.09.24.461537] [Reference Citation Analysis]
22 Thakur A, Ke X, Chen YW, Motallebnejad P, Zhang K, Lian Q, Chen HJ. The mini player with diverse functions: extracellular vesicles in cell biology, disease, and therapeutics. Protein Cell 2021. [PMID: 34374936 DOI: 10.1007/s13238-021-00863-6] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 25.0] [Reference Citation Analysis]
23 Zhang H, Shang R, Bi P. Feedback regulation of Notch signaling and myogenesis connected by MyoD-Dll1 axis. PLoS Genet 2021;17:e1009729. [PMID: 34370738 DOI: 10.1371/journal.pgen.1009729] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
24 Martins T, Meng Y, Korona B, Suckling R, Johnson S, Handford PA, Lea SM, Bray SJ. The conserved C2 phospholipid-binding domain in Delta contributes to robust Notch signalling. EMBO Rep 2021;:e52729. [PMID: 34347930 DOI: 10.15252/embr.202152729] [Reference Citation Analysis]
25 Zeronian MR, Klykov O, Portell I de Montserrat J, Konijnenberg MJ, Gaur A, Scheltema RA, Janssen BJC. Notch-Jagged signaling complex defined by an interaction mosaic. Proc Natl Acad Sci U S A 2021;118:e2102502118. [PMID: 34301900 DOI: 10.1073/pnas.2102502118] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
26 Ng HL, Quail E, Cruickshank MN, Ulgiati D. To Be, or Notch to Be: Mediating Cell Fate from Embryogenesis to Lymphopoiesis. Biomolecules 2021;11:849. [PMID: 34200313 DOI: 10.3390/biom11060849] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Bott LC, Forouhan M, Lieto M, Sala AJ, Ellerington R, Johnson JO, Speciale AA, Criscuolo C, Filla A, Chitayat D, Nemeth AH, Angelucci F, Lim WF, Striano P, Zara F, Helbig I, Muona M, Courage C, Lehesjoki A, Berkovic SF, Fischbeck KH, Brancati F, Morimoto RI, Wood MJ, Rinaldi C, Italian Undiagnosed Diseases Network, V-ATPase Consortium. Biallelic and de novo variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.. [DOI: 10.1101/2021.06.01.21257500] [Reference Citation Analysis]
28 Chapman G, Moreau JLM, I P E, Szot JO, Iyer KR, Shi H, Yam MX, O'Reilly VC, Enriquez A, Greasby JA, Alankarage D, Martin EMMA, Hanna BC, Edwards M, Monger S, Blue GM, Winlaw DS, Ritchie HE, Grieve SM, Giannoulatou E, Sparrow DB, Dunwoodie SL. Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants. Hum Mol Genet 2020;29:566-79. [PMID: 31813956 DOI: 10.1093/hmg/ddz270] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 21.0] [Reference Citation Analysis]
29 Han X, Xiong X, Shi X, Chen F, Li Y. Targeted sequencing of NOTCH signaling pathway genes and association analysis of variants correlated with mandibular prognathism. Head Face Med 2021;17:17. [PMID: 34039391 DOI: 10.1186/s13005-021-00268-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Condorelli AG, El Hachem M, Zambruno G, Nystrom A, Candi E, Castiglia D. Notch-ing up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway. J Biomed Sci 2021;28:36. [PMID: 33966637 DOI: 10.1186/s12929-021-00732-8] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
31 Coppens S, Barnard AM, Puusepp S, Pajusalu S, Õunap K, Vargas-Franco D, Bruels CC, Donkervoort S, Pais L, Chao KR, Goodrich JK, England EM, Weisburd B, Ganesh VS, Gudmundsson S, O'Donnell-Luria A, Nigul M, Ilves P, Mohassel P, Siddique T, Milone M, Nicolau S, Maroofian R, Houlden H, Hanna MG, Quinlivan R, Beiraghi Toosi M, Ghayoor Karimiani E, Costagliola S, Deconinck N, Kadhim H, Macke E, Lanpher BC, Klee EW, Łusakowska A, Kostera-Pruszczyk A, Hahn A, Schrank B, Nishino I, Ogasawara M, El Sherif R, Stojkovic T, Nelson I, Bonne G, Cohen E, Boland-Augé A, Deleuze JF, Meng Y, Töpf A, Vilain C, Pacak CA, Rivera-Zengotita ML, Bönnemann CG, Straub V, Handford PA, Draper I, Walter GA, Kang PB. A form of muscular dystrophy associated with pathogenic variants in JAG2. Am J Hum Genet 2021;108:840-56. [PMID: 33861953 DOI: 10.1016/j.ajhg.2021.03.020] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
32 Roifman M, Chung BHY, Reid DM, Teitelbaum R, Martin N, Nield LE, Thompson M, Shannon P, Chitayat D. Heterozygous NOTCH1 deletion associated with variable congenital heart defects. Clin Genet 2021;99:836-41. [PMID: 33630301 DOI: 10.1111/cge.13948] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
33 Hankeova S, Van Hul N, Laznovsky J, Mangold K, Hensens N, Verhoef E, Zikmund T, Dawit F, Kavkova M, Salplachta J, Sjöqvist M, Johansson BR, Hassan M, Fredriksson L, Bryja V, Lendahl U, Jheon A, Alten F, Fahnehjelm KT, Fischler B, Kaiser J, Andersson ER. Sex differences and risk factors for bleeding in Alagille syndrome.. [DOI: 10.1101/2021.04.13.439679] [Reference Citation Analysis]
34 Kim E, Kim JY, Kim S, Ham SW, Choi S, Hong N, Park MG, Jang J, Seo S, Lee K, Jeong HJ, Kim SJ, Jeong S, Min K, Kim S, Jin X, Kim SH, Kim S, Kim H. JAG1 intracellular domain acts as a transcriptional cofactor that forms an oncogenic transcriptional complex with DDX17/SMAD3/TGIF2.. [DOI: 10.1101/2021.03.31.437839] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
35 Surkova S, Görne J, Nuzhdin S, Samsonova M. Interplay between sex determination cascade and major signaling pathways during Drosophila eye development: Perspectives for future research. Dev Biol 2021;476:41-52. [PMID: 33745943 DOI: 10.1016/j.ydbio.2021.03.005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
36 Tanimizu N. The neonatal liver: Normal development and response to injury and disease. Semin Fetal Neonatal Med 2021;:101229. [PMID: 33745829 DOI: 10.1016/j.siny.2021.101229] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
37 Hankeova S, Salplachta J, Zikmund T, Kavkova M, Van Hul N, Brinek A, Smekalova V, Laznovsky J, Dawit F, Jaros J, Bryja V, Lendahl U, Ellis E, Nemeth A, Fischler B, Hannezo E, Kaiser J, Andersson ER. DUCT reveals architectural mechanisms contributing to bile duct recovery in a mouse model for Alagille syndrome. Elife 2021;10:e60916. [PMID: 33635272 DOI: 10.7554/eLife.60916] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
38 Hamdi-Rozé H, Ware M, Guyodo H, Rizzo A, Ratié L, Rupin M, Carré W, Kim A, Odent S, Dubourg C, David V, de Tayrac M, Dupé V. Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency. J Clin Endocrinol Metab 2020;105:dgaa249. [PMID: 32403133 DOI: 10.1210/clinem/dgaa249] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
39 Zeronian MR, Klykov O, de Montserrat JPI, Konijnenberg MJ, Gaur A, Scheltema RA, Janssen BJ. Notch-Jagged signaling complex defined by an interaction mosaic.. [DOI: 10.1101/2021.02.19.432005] [Reference Citation Analysis]
40 Martins T, Meng Y, Korona B, Suckling R, Johnson S, Handford P, Lea SM, Bray S. Delta C2 Domain β1-2 loop contributes to robust Notch signalling.. [DOI: 10.1101/2021.02.16.431397] [Reference Citation Analysis]
41 Torres HM, Rodezno-Antunes T, VanCleave A, Cao Y, Callahan DL, Westendorf JJ, Tao J. Precise detection of a murine germline mutation of the Notch3 gene associated with kyphosis and developmental disorders. J Adv Vet Anim Res 2021;8:7-13. [PMID: 33860007 DOI: 10.5455/javar.2021.h479] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Ahmed S, Arif A, Abbas S, Khan MO, Kirmani S, Khan AH. Hajdu Cheney Syndrome due to NOTCH2 defect - First case report from Pakistan and review of literature. Ann Med Surg (Lond) 2021;62:154-9. [PMID: 33520214 DOI: 10.1016/j.amsu.2021.01.041] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
43 Ristori T, Sjöqvist M, Sahlgren CM. Ex Vivo Models to Decipher the Molecular Mechanisms of Genetic Notch Cardiovascular Disorders. Tissue Eng Part C Methods 2021;27:167-76. [PMID: 33403934 DOI: 10.1089/ten.TEC.2020.0327] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
44 Stassen OMJA, Ristori T, Sahlgren CM. Notch in mechanotransduction - from molecular mechanosensitivity to tissue mechanostasis. J Cell Sci 2020;133:jcs250738. [PMID: 33443070 DOI: 10.1242/jcs.250738] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 12.0] [Reference Citation Analysis]
45 Conith AJ, Hope SA, Chhouk BH, Craig Albertson R. Weak genetic signal for phenotypic integration implicates developmental processes as major regulators of trait covariation. Mol Ecol 2021;30:464-80. [PMID: 33231336 DOI: 10.1111/mec.15748] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
46 Höving AL, Sielemann K, Greiner JFW, Kaltschmidt B, Knabbe C, Kaltschmidt C. Transcriptome Analysis Reveals High Similarities between Adult Human Cardiac Stem Cells and Neural Crest-Derived Stem Cells. Biology (Basel) 2020;9:E435. [PMID: 33271866 DOI: 10.3390/biology9120435] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
47 Deshpande SS, Nemani H, Arumugam G, Ravichandran A, Balasinor NH. High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats. Clin Epigenetics 2020;12:179. [PMID: 33213487 DOI: 10.1186/s13148-020-00974-7] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
48 Reichrath J, Reichrath S. The Impact of Notch Signaling for Carcinogenesis and Progression of Nonmelanoma Skin Cancer: Lessons Learned from Cancer Stem Cells, Tumor Angiogenesis, and Beyond. Adv Exp Med Biol 2021;1287:123-54. [PMID: 33034030 DOI: 10.1007/978-3-030-55031-8_9] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
49 Zohorsky K, Mequanint K. Designing Biomaterials to Modulate Notch Signaling in Tissue Engineering and Regenerative Medicine. Tissue Eng Part B Rev 2021;27:383-410. [PMID: 33040694 DOI: 10.1089/ten.TEB.2020.0182] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
50 Kobia FM, Preusse K, Dai Q, Weaver N, Hass MR, Chaturvedi P, Stein SJ, Pear WS, Yuan Z, Kovall RA, Kuang Y, Eafergen N, Sprinzak D, Gebelein B, Brunskill EW, Kopan R. Notch dimerization and gene dosage are important for normal heart development, intestinal stem cell maintenance, and splenic marginal zone B-cell homeostasis during mite infestation. PLoS Biol 2020;18:e3000850. [PMID: 33017398 DOI: 10.1371/journal.pbio.3000850] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
51 Arefin B, Parvin F, Bahrampour S, Stadler CB, Thor S. Drosophila Neuroblast Selection Is Gated by Notch, Snail, SoxB, and EMT Gene Interplay. Cell Rep 2019;29:3636-3651.e3. [PMID: 31825841 DOI: 10.1016/j.celrep.2019.11.038] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 8.0] [Reference Citation Analysis]
52 Pandey A, Harvey BM, Lopez MF, Ito A, Haltiwanger RS, Jafar-Nejad H. Glycosylation of Specific Notch EGF Repeats by O-Fut1 and Fringe Regulates Notch Signaling in Drosophila. Cell Rep 2019;29:2054-2066.e6. [PMID: 31722217 DOI: 10.1016/j.celrep.2019.10.027] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 7.5] [Reference Citation Analysis]
53 Lee SH, Reed-newman T, Anant S, Ramasamy TS. Regulatory Role of Quiescence in the Biological Function of Cancer Stem Cells. Stem Cell Rev and Rep 2020;16:1185-207. [DOI: 10.1007/s12015-020-10031-8] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
54 Kakuda S, LoPilato RK, Ito A, Haltiwanger RS. Canonical Notch ligands and Fringes have distinct effects on NOTCH1 and NOTCH2. J Biol Chem 2020;295:14710-22. [PMID: 32820046 DOI: 10.1074/jbc.RA120.014407] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 11.5] [Reference Citation Analysis]
55 Xue AG, Chan M, Gujral TS. Pan-cancer analysis of the developmental pathways reveals non-canonical wnt signaling as a driver of mesenchymal-type tumors. Transl Res 2020;224:1-15. [PMID: 32522670 DOI: 10.1016/j.trsl.2020.06.003] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
56 Pandey A, Niknejad N, Jafar-Nejad H. Multifaceted regulation of Notch signaling by glycosylation. Glycobiology 2021;31:8-28. [PMID: 32472127 DOI: 10.1093/glycob/cwaa049] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
57 Mota M, Shevde LA. Merlin regulates signaling events at the nexus of development and cancer. Cell Commun Signal 2020;18:63. [PMID: 32299434 DOI: 10.1186/s12964-020-00544-7] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
58 Moscatelli G, Bovo S, Schiavo G, Mazzoni G, Bertolini F, Dall'Olio S, Fontanesi L. Genome-wide association studies for iris pigmentation and heterochromia patterns in Large White pigs. Anim Genet 2020;51:409-19. [PMID: 32232994 DOI: 10.1111/age.12930] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
59 Reichrath J, Reichrath S. Notch Signaling and Embryonic Development: An Ancient Friend, Revisited. Adv Exp Med Biol 2020;1218:9-37. [PMID: 32060869 DOI: 10.1007/978-3-030-34436-8_2] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 8.0] [Reference Citation Analysis]
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