R. D. Del Mastro

发表

The use of direct cDNA selection to rapidly and effectively identify genes in the fungus Aspergillus fumigatus.

Q. Zeng, L. Doucette‐Stamm, Luquan Wang, 2002, Fungal genetics and biology : FG & B.

Mouse ADAM33: two splice variants differ in protein maturation and localization.

F. Gheyas, Y. Wan, S. Umland, 2004, American journal of respiratory cell and molecular biology.

Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.

D. Viljoen, R. Devereux, B. Sykes, 1992, The New England journal of medicine.

Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotation.

J. McPherson, M. Lovett, J. Wasmuth, 1995, Genome research.

A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait.

Mark L. Johnson, P. van Eerdewegh, J. Carulli, 2002, American journal of human genetics.

Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.

I. Glass, W. Lanyon, J. Connor, 1992, American journal of medical genetics.

Isolation of coding sequences from genomic regions using direct selection.

M. Lovett, R. D. Del Mastro, 1997, Methods in molecular biology.

A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.

C Junien, M Sarfarazi, P Farndon, 1992, Journal of medical genetics.

Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene

P. van Eerdewegh, T. Keith, R. D. Little, 2007, BMC Medical Genetics.

A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.

D. Church, J. McPherson, M. Lovett, 1997, Genome research.

A high-throughput and sensitive method to measure Global DNA Methylation: Application in Lung Cancer

P. Massion, Hui Huang, A. Anisowicz, 2008, BMC Cancer.

Adrenoleucodystrophy: a molecular genetic study in five families.

M. Kilpatrick, R. D. Del Mastro, S. Bundey, 1990, Journal of medical genetics.

Analytical validation of a novel panel of biomarkers for a test for preeclampsia.

P. Oberoi, Emad Bahrami-Samani, M. Abbasi, 2022, Journal of pharmaceutical and biomedical analysis.

MinimuMM-seq: Genome sequencing of circulating tumor cells for minimally invasive molecular characterization of multiple myeloma pathology.

Andrew J. Dunford, C. Stewart, D. Auclair, 2022, Cancer discovery.