Disease relevance of ATP6V1H

• In summary, the newborn with less than 37 weeks of gestation and below 2,000 grams of birth weight would be named and classified as a SFD (small for dates) with the problem for mental development (MD-SFD) [1].

Psychiatry related information on ATP6V1H

• Attention and memory for somatic symptom and IEI-trigger words was compared among participants with IEI (n = 54), somatoform disorders (SFD; n = 44) and control participants (n = 54) [2].

High impact information on ATP6V1H

• Since it shares sequence similarity with the catalytic subunit of the vacuolar ATPase (V-ATPase) and complements the loss of this VMA13 gene in yeast, NBP1 is the human homolog of Vma13p [3].
• In addition, the drugs suppressed the cellular activation-associated cell surface expression of a putative Nef-binding protein in PBMC, although they had no influence on its expression in cell line cells [4].
• These results suggest that the 25-kDa protein on murine cell surfaces corresponds to the human Nef binding protein and is responsible for the Nef-induced apoptosis, and that its expression on the cell surface depends on cellular activation [5].
• Early growth of term SFD infants in relation to caloric intake [6].

Analytical, diagnostic and therapeutic context of ATP6V1H

• Using mouse monoclonal antibodies (mAbs) against the human Nef-binding protein and flow cytometry, we analyzed the expression of a corresponding protein on murine cells [5].
• The IgG, IgA and IgM levels were determined by the technique of radial immunodiffusion of Mancini et al. in 40 SFD and 30 normal control newborn infants [7].

References