P. Patel

发表

Human 12(R)-Lipoxygenase and the Mouse Ortholog

P. Patel, M. McDonnell, Hongwei Li, 1998, The Journal of Biological Chemistry.

B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.

V. Torres, P. Harris, K. Hopp, 2011, Human molecular genetics.

Fine structure of the human hypoxanthine phosphoribosyltransferase gene

A. C. Chinault, C. Caskey, P. Framson, 1986, Molecular and cellular biology.

Cloning of a human “epidermal-type” 12-lipoxygenase-related gene and chromosomal localization to 17p13

S. Elsea, D. Sun, P. Patel, 1998, Cytogenetic and Genome Research.

Functional characterization of the human hypoxanthine phosphoribosyltransferase gene promoter: evidence for a negative regulatory element

D. Rincon-Limas, P. Patel, D. Krueger, 1991, Molecular and cellular biology.

5′‐flanking sequences of the human HPRT gene direct neuronal expression in the brain of transgenic mice

P. Patel, D. Rincon-Limas, P. Overbeek, 1994, Journal of neuroscience research.

Ubiquitous and neuronal DNA-binding proteins interact with a negative regulatory element of the human hypoxanthine phosphoribosyltransferase gene

D. Rincon-Limas, M. L. Nino-Rosales, F. Amaya-Manzanares, 1995, Molecular and cellular biology.

Competitive binding of triplex-forming oligonucleotides in the two alternate promoters of the PMP22 gene.

S. Bidichandani, M. Hogan, P. Patel, 2001, Antisense & nucleic acid drug development.

Recombination hot spots and human disease.

P. Patel, S. Purandare, Smita M. Purandare, 1997, Genome research.

The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.

A. Baldini, C. Caskey, S. Jiralerspong, 1995, Human molecular genetics.

Expression of human and mouse HPRT minigenes.

A. C. Chinault, C. Caskey, D. Melton, 1986, Advances in experimental medicine and biology.

Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence.

R. Gibbs, S. Bidichandani, S. Purandare, 1999, Human molecular genetics.

Erratum to the report of the third international workshop on human Y chromosome mapping 1997

A. Uitterlinden, E. Mullaart, A. Protopopov, 1997 .

Assignment1 of Big MAP Kinase (PRKM7) to human chromosome 17 band p11.2 with somatic cell hybrids

P. Patel, J.-D. Lee, S. Purandare, 1998, Cytogenetic and Genome Research.

The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases.

W. Reardon, R. Winter, S. Malcolm, 1997, Human molecular genetics.

Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.

P. Patel, C. Gellera, P. Cavadini, 2000, Human molecular genetics.