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Spinocerebellar ataxia type 48: last but not least.

• Authors : De Michele, Giovanna (AUTHOR); Galatolo, Daniele (AUTHOR); Barghigiani, Melissa (AUTHOR)

Subjects: SPINOCEREBELLAR ataxia; UBIQUITIN ligases; SYMPTOMS

• Source: Neurological Sciences. Sep2020, Vol. 41 Issue 9, p2423-2432. 10p. 2 Diagrams, 1 Chart.

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Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.

• Authors : Nakano, Kiyoshi¹ (AUTHOR); Kubota, Yasuo^1,2 (AUTHOR) ; Mori, Takayuki^1,2 (AUTHOR)

Subjects: *UBIQUITIN ligases; *GENETIC mutation; *FAMILIAL hypercholesterolemia

• Source: Nephrology. Nov2020, Vol. 25 Issue 11, p818-821. 4p.

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Tag Team Ubiquitin Ligases.

• Authors : Kleiger, Gary¹; Deshaies, Raymond^2,3

Subjects: *UBIQUITIN ligases; *ENZYMES; *GENETIC mutation

• Source: Cell. Aug2016, Vol. 166 Issue 5, p1080-1081. 2p.

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Comprehensive analysis of the expression and prognosis for RBR E3 ubiquitin ligases in lung adenocarcinoma.

• Authors : Ding, Hao; Wang, Yuxin; Cui, Yuan

Subjects: LUNG cancer & genetics; ENZYME metabolism; LUNG cancer

• Source: Thoracic Cancer; Sep2022, Vol. 13 Issue 17, p2459-2472, 14p

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E3 Ubiquitin Ligases in Neurological Diseases: Focus on Gigaxonin and Autophagy.

• Authors : Lescouzères, Léa; Bomont, Pascale

Subjects: UBIQUITIN ligases; NEUROLOGICAL disorders; PROTEOLYSIS

• Source: Frontiers in Physiology; 10/22/2020, Vol. 11, pN.PAG-N.PAG, 25p

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Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome.

• Authors : Cheol-Sang Hwang^1,2; Sukalo, Maja³; Batygin, Olga¹

Subjects: *UBIQUITIN ligases; *GENETIC disorders; *GENETIC mutation

• Source: PLoS ONE. 2011, Vol. 6 Issue 9, p1-10. 10p.

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The CRL4 E3 ligase Mahjong/DCAF1 controls cell competition through the transcription factor Xrp1, independently of polarity genes.

• Authors : Kumar, Amit¹; Baker, Nicholas E.¹

Subjects: *TRANSCRIPTION factors; *UBIQUITIN ligases; *RIBOSOMAL proteins

• Source: Development (09501991). Nov2022, Vol. 149 Issue 22, p1-13. 13p.

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A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia.

• Authors : Wu, Huan^1,2,3 (AUTHOR); Zhang, Xin⁴ (AUTHOR); Shen, Qunshan^1,5,6 (AUTHOR)

Subjects: *GENETIC mutation; *UBIQUITIN ligases; *NONSENSE mutation

• Source: Clinical Genetics. Jan2022, Vol. 101 Issue 1, p55-64. 10p.

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Polymorphism of P53-Ets/ AP1 transactivation region of MDM2 oncogene and its immunohistochemical analysis in canine tumours.

• Authors : Rezaie, A.¹; Tabandeh, M. R.²; Noori, S. M. A.²

Subjects: *GENETIC polymorphism research; *UBIQUITIN ligases; *IMMUNOHISTOCHEMISTRY

• Source: Veterinary & Comparative Oncology. Jun2016, Vol. 14 Issue 2, p137-146. 10p.

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Education Full Text (H.W. Wilson)

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