Andrew J. Hartung

The Tabby phenotype is caused by mutation in a mouse homologue of the <i>EDA</i> gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Anand K. Srivastava, Johanna Pispa, Andrew J. Hartung et al. · Proceedings of the National Academy of Sciences · 1997 · 312 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats

Mónica Bayés, Andrew J. Hartung, Sini Ezer et al. · Human Molecular Genetics · 1998 · 229 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Molecular Cloning and Characterization of TRPC5 (HTRP5), the Human Homologue of a Mouse Brain Receptor-Activated Capacitative Ca2+ Entry Channel

Khalid Sossey‐Alaoui, Jennifer A. Lyon, Latonya Jones et al. · Genomics · 1999 · 74 citations

Life Sciences, Molecular Biology, Neuroscience +14

Characterization of DNA sequences encoding a novel isoform of the 55 kDa B regulatory subunit of the type 2A protein serine/threonine phosphatase of Arabidopsis thaliana

John W. Corum, Andrew J. Hartung, Robin T. Stamey et al. · Plant Molecular Biology · 1996 · 34 citations

Life Sciences, Genetics, Molecular Biology +12

From ectodermal dysplasia to selective tooth agenesis

Gabriele Mues, Rachel Griggs, Andrew J. Hartung et al. · American Journal of Medical Genetics Part A · 2009 · 33 citations

Life Sciences, Genetics, Molecular Genetics +16