Donna Durham‐Pierre

University of Arizona — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index820citations14works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

melanin and skin pigmentation(8), Biochemical Analysis and Sensing Techniques(8), Epigenetics and DNA Methylation(4), Genomics and Chromatin Dynamics(3), RNA Interference and Gene Delivery(2)

Publications14 total

A very large protein with diverse functional motifs is deficient in <i>rjs</i> (runty, jerky, sterile) mice
Proceedings of the National Academy of Sciences·1998· 93 cited
Mutations of the human P gene associated with type II oculocutaneous albinism (OCA2)
Human Mutation·1998· 35 cited
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.
Human Mutation·1998· 23 cited
Mutations of the human P gene associated with type II oculocutaneous albinism (OCA2)
Human Mutation·1998· 12 cited
Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene
Human Genetics·1997· 39 cited
Oculocutaneous albinism in an isolated Tonga community in Zimbabwe.
Journal of Medical Genetics·1997· 49 citedOpen Access
Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African‐Americans
Human Mutation·1996
Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African‐Americans
Human Mutation·1996· 23 cited
Melanosomal Tyrosine Transport in Normal and Pink‐eyed Dilution Murine Melanocytes
Pigment Cell Research·1995· 51 cited
Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene.
Proceedings of the National Academy of Sciences·1994· 145 citedOpen Access
The Mouse Pink‐Eyed Dilution Gene: Association with Hypopigmentation in Prader‐Willi and Angelman Syndromes and with Human OCA2
Pigment Cell Research·1994· 30 cited
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism
Nature Genetics·1994· 122 cited
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus
Nature·1993· 104 cited
High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation.
Proceedings of the National Academy of Sciences·1993· 94 citedOpen Access

Frequent Co-authors

Murray H. Brilliant(12), Yoshimichi Nakatsu(6), Richard A. King(6), John M. Gardner(5), Ada Ching(5), Uta Francke(2), R Aquaron(2), Patricia Lund(2), J. P. Fryer(2), John M. Naber(2), Steve Laken(2), Julie Meeks Gardner(2), Susana Rosemblat(1), Seth J. Orlow(1), V. del Mármol(1), Rachel F. Tyndale(1), Timothy M. DeLorey(1), Heather J. McDanel(1), Quy Tu Nguyen(1), Joseph Wagstaff(1)