Hydroxymethylbilane

Europe PMC · from cache · sorted by publication date

1. 1
   Limited benefit of liver transplantation in a boy with biallelic severe deficiency of hydroxymethylbilane synthase and review of prior reported cases.

   Araque M, Ma CD, Jordan A, Faust D, McGuire L, Bonkovsky HL. · 2026-06-27

   unreviewed
2. 2
   Reconstructing the hydrogenobyrinic acid synthetic toolkit by combining cell-free systems and metabolic engineering.

   Lv R, Kang Q, Wang J, Luo X, Zhang D. · 2026-02-02

   open access unreviewed
3. 3
   Threonine and glutamine in ovo supplementation affects post-hatch development and expression of genes related to the first line of defense of the intestinal mucosa in broiler chickens.

   Santos WS, Sousa AV, Gomes DS, Marinho GF, Oliveria TJ, Givisiez PEN, Oliveira CJB, Malheiros RD, Filho ALBM. · 2026-04-22

   open access unreviewed
4. 4
   Updates to gene-disease classifications and inheritance patterns for porphyrias.

   Reeves EB, Hankey W, Clair PS, Goldstein JL, Wilke MVMB, Feigenbaum A, Hung C, Spector E, Craigen WJ. · 2026-04-30

   unreviewed
5. 5
   A Case Report of Acute Intermittent Porphyria Accompanied by Severe Peripheral Neuropathy

   Liu Y, Cao J, Han F, Chen Q, You H, Zhu H, Li Y, Liu A, Yang J. · 2026-06-01

   open access unreviewed
6. 6
   5-ALA in Oncology: Current Clinical Applications, Biological Limitations, and Emerging Translational Strategies

   Inglot J, Bartusik-Aebisher D, Myśliwiec A, Dynarowicz K, Paul A, Xavierselvan M, Aebisher D. · 2026-06-01

   open access unreviewed
7. 7
   Matrix- and Differentiation Stage-Dependent Variability of Reference Genes: Rethinking Validation Strategies in 3T3-L1 Adipogenic Models

   · 2026-06-01

   open access unreviewed
8. 8
   Mechanisms underlying green flower formation.

   Li X, Hong C, Li H, Hou S, Sun Q, Zang Y, Sun G, Huang Z, Gao H. · 2026-03-03

   open access unreviewed
9. 9
   Glycine: The missing link between carbohydrate and xenobiotic metabolism in the maturing human hepatocyte.

   Pozo Garcia V, Çobanoğlu TS, Riga K, Sharma S, Jennings P, Vos JC, Moco S. · 2026-05-28

   open access unreviewed
10. 10
    Molecular analysis of a new patient COX15 mutation provides insight into the etiology of fatal infantile cardioencephalopathy.

    Carroll-Deaton JA, Bohovych I, Emetu FT, Dietz JV, Rivett ED, Stanley E, Hegg EL, Fox JL, Khalimonchuk O. · 2026-04-17

    open access unreviewed

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