Below are the most recent publications written about "Phenotype" by people in Profiles.
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Tripathi S, Jul? AM, Zhuo Z, Schreiber BL, Martin-Moreno PL, Sui SH, Waaga-Gasser AM, Chandraker A. Single-cell and multi-omic characterization of ex vivo expanded ASTRLs from stable kidney transplant recipients reveals a regulatory T cell phenotype. Sci Rep. 2026 Jan 14; 16(1):3619.
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Choi HL, Kim B, Park YM, Yoo JE, Kim S, Jeong SM, Han K, Shin DW. Metabolic obesity phenotypes and breast cancer risk before and after menopause: A nationwide cohort study in South Korea. Cancer. 2026 01 01; 132(1):e70244.
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Koon AC, Yeung KYW, Wu Y, Leong LI, Cheung JTP, Chen ZS, Peng SI, Armstrong NS, Frank CA, Magneron P, Gomes-Pereira M, Fung JMS, Bargiela A, Moreno N, Poyatos-Garcia J, Vilchez J, Huguet-Lachon A, Brewer CK, Zinter M, Beck ES, Artero R, Gourdon G, Budnik V, Thomson T, McCabe BD, Chan HYE. Pre- and postsynaptic upregulation of FasII synergistically underlies neuropathological and behavioral phenotypes in a Drosophila model of myotonic dystrophy. Nat Commun. 2025 Dec 18; 17(1):1005.
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Lord KA, Sohrab V, Bryc K, White ME, Kenney B, Morrill Pirovich K, Chen FL, Karlsson EK. Genetic testing predicts appearance but not behavior in dogs. Proc Natl Acad Sci U S A. 2025 Dec 02; 122(48):e2421752122.
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Calhoun CCS, Capps MES, Muya K, Gannaway WC, Martina V, Conklin CL, Klein MC, Webster JM, Torija-Olson EG, Thyme SB. Removal of developmentally regulated microexons has a minimal impact on larval zebrafish brain morphology and function. Elife. 2025 Nov 18; 13.
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Ryerson CJ, Bankier A, Beasley MB, Brown K, Colby T, Cottin V, Desai S, Galvin J, Haramati LB, Hariri LP, Inoue Y, Johkoh T, Lee HY, Leung A, Lynch D, Muller N, Nicholson A, Raoof S, Revel MP, Remy-Jardin M, Richeldi L, Ryu JH, Schiebler M, Sholl L, Sverzellati N, Travis W, Walsh SLF, Wells AU, White CS, Johannson KA. Standardized Clinical Terms and Definitions for Interstitial Lung Disease: A Consensus Statement from the Fleischner Society. Am J Respir Crit Care Med. 2025 Oct; 211(10):1756-1774.
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Welton JM, Tremblay KD, Mager J. Loss of CMTR1 leads to gastrulation failure and early embryonic lethality. Dev Biol. 2025 Dec; 528:1-12.
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Narvaez-Guerra O, Botros M, Offord E, Aurigemma G. Phenotypic overlap in apical hypertrophic cardiomyopathy: one size does not fit all. BMJ Case Rep. 2025 Aug 27; 18(8).
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Hengel H, Hannan SB, Reich S, Beijer D, Roller J, Gilsbach BK, Gloeckner CJ, Greene D, Timmann D, Depienne C, Mumford A, O'Driscoll M, Nemeth AH, Lundberg J, Rodan LH, Bruel AL, Delanne J, Deconinck T, Baets J, Gan-Or Z, Rouleau G, Suchowersky O, Estiar MA, Reich S, Toro C, Z?chner S, Hazan J, P?tursson H, Harmuth F, Bauer C, Bauer P, Turro E, Lambright D, Sch?ls L, Synofzik M. Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism. Brain. 2025 Aug 01; 148(8):2812-2826.
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Iwanowicz A, Boudi A, Seeley C, Sapp E, Miller R, Liu S, Chase K, Shing K, Batista AR, Siena-Esteves M, Aronin N, DiFiglia M, Kegel-Gleason KB. Intrastriatal Delivery of a Zinc Finger Protein Targeting the Mutant HTT Gene Allele Obviates Lipid Phenotypes in Brain and Plasma in Huntington's Disease?Mice. Hum Gene Ther. 2025 Aug; 36(15-16):1083-1094.