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Turnover of two lysosomal enzymes in macrophages

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The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene.

Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico.

cDNA sequence and mapping of the mouse Copb gene encoding the beta subunit of the COPI coatomer complex.

Porphyromonas gingivalis platelet aggregation activity: outer membrane vesicles are potent activators of murine platelets.

5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene.

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.

The black fly salivary protein Simukunin inhibits complement activation through the lectin pathway protease MASP-2.

The BAIAP2 Pathway Regulates Proliferation and Migration in Medulloblastoma.

Targeting PGAM1 Y119 Phosphorylation Resensitizes Non-Small Cell Lung Cancer to Cisplatin Therapy by Promoting Oxidative Stress and DNA Damage.

M6PR/IGF2R double-knockout supplies therapeutic sources for mucolipidosis II and Niemann-Pick C2.

ZBTB38 requires an extended N-terminal zinc finger network to read mCpG- and discriminate TpG-containing DNA sequences.

In vitro reconstitution implicates multiple OMP assembly factors in CdiAEC93 toxin delivery.

Why is the chloroplast redox regulatory machinery so complex?

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