Fengmin Lu

Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients

I. Krantz, N. Spinner, D. Piccoli, 2001, Human mutation.

Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage.

N. Spinner, J. Morrissette, Fengmin Lu, 2003, American journal of human genetics.

Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletion.

I. Krantz, N. Spinner, D. Piccoli, 2002, American journal of medical genetics.

Rep/Cap gene amplification and high-yield production of AAV in an A549 cell line expressing Rep/Cap.

N. Spinner, James M. Wilson, G. Gao, 2002, Molecular therapy : the journal of the American Society of Gene Therapy.

Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher–Schinzel (3C) syndrome

I. Krantz, N. Spinner, A. Toutain, 2005, American journal of medical genetics. Part A.