L. Singer

Nuclear polyglutamine-containing protein aggregates as active proteolytic centers

A. von Mikecz, Min Chen, L. Singer, 2008, The Journal of cell biology.

A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.

H. Colten, H. Dietz, D. Demello, 1994, The Journal of clinical investigation.

Inherited human complement C3 deficiency. An amino acid substitution in the beta-chain (ASP549 to ASN) impairs C3 secretion.

Z. Fishelson, H. Akama, R. Wetsel, 1994, The Journal of biological chemistry.

The levels of galactosyltransferase activity in sera from normal children and patients with cystic fibrosis.

M. Moscarello, D. Crozier, L. Singer, 1974, Clinical biochemistry.

Complement C3 deficiency: human, animal, and experimental models.

H. Colten, R. Wetsel, L. Singer, 1994, Pathobiology : journal of immunopathology, molecular and cellular biology.

Inherited complement C3 deficiency: reduced C3 mRNA and protein levels in a Laotian kindred.

M. Lokki, R. Wetsel, J. Kramer, 1996, Clinical immunology and immunopathology.