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BLOC1S5 gene

Known as: dJ303A1.3, BIOGENESIS OF LYSOSOME-RELATED ORGANELLES COMPLEX 1, SUBUNIT 5, BLOS5 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Hermansky–Pudlak syndrome (HPS) is characterized by oculocutaneous albinism, excessive bleeding, and often additional symptoms… Expand
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2014
2014
Background: Dysbindin-1 isoforms are selectively reduced in schizophrenic brains. Results: Dysbindin-1C is required for the… Expand
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Highly Cited
2004
Highly Cited
2004
The purpose of the present study was to examine gravity receptor function in mutant mouse strains with variable deficits in… Expand
2004
2004
The recessive muted (mu) and pearl (pe) mutations on Chromosome (Chr) 13 cause pigment dilution and platelet storage pool… Expand
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Highly Cited
2003
Highly Cited
2003
Hermansky-Pudlak syndrome (HPS) is a disorder of organelle biogenesis affecting 3 related organelles-melanosomes, platelet dense… Expand
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Highly Cited
2002
Highly Cited
2002
  • Q. Zhang, Wei Li, +6 authors R. Swank
  • Human molecular genetics
  • 2002
  • Corpus ID: 32278860
The muted (mu) mouse is a model for Hermansky-Pudlak Syndrome (HPS), an inherited disorder of humans causing hypopigmentation… Expand
2002
2002
Mu (mu) opioid agonists preferentially increase the intake of highly palatable food. Here we investigated changes in mu opioid… Expand
Highly Cited
1988
Highly Cited
1988
The effects of highly selective mu and delta opioid peptide agonists were determined in two rat models of experimentally-induced… Expand
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1980
1980
Abstract Randomly sheared fragments of Mu cts 62 DNA have been cloned into the Eco RI cleavage site of plasmid p0P203(UV-5)-3, a… Expand
1978
1978
To determine whether the early replication of Mu prophage DNA proceeds beyond the termini of the prophage into hose DNA, the… Expand