M. Gorry

发表

Structure and sequence of human FGF8.

J. Gemel, M. Gorry, G. Ehrlich, 1996, Genomics.

A rationally designed A34R mutant oncolytic poxvirus: improved efficacy in peritoneal carcinomatosis.

M. Gorry, D. Bartlett, S. Thorne, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients

T C Hart, M. Gorry, T. Hart, 2003, Genes and Immunity.

Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

B. Devlin, M. Gorry, G. Ehrlich, 1999, American journal of human genetics.

Evidence of bacterial metabolic activity in culture-negative otitis media with effusion.

Y. Chen, M. Gorry, G. Ehrlich, 1998, JAMA.

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

T C Hart, M. Gorry, B. Shirts, 2002, Journal of medical genetics.

Clinico-pathologic findings in medullary cystic kidney disease type 2

M. Willingham, M. Gorry, H. Trachtman, 2005, Pediatric Nephrology.

Aquaporin Expression in Developing Human Teeth and Selected Orofacial Tissues

M. Gorry, T. Hart, N. Piesco, 2003, Calcified Tissue International.

RNA differential display of scarless wound healing in fetal rabbit indicates downregulation of a CCT chaperonin subunit and upregulation of a glycophorin-like gene transcript.

H. S. Li, D. Dressman, P. Hebda, 2000, Journal of pediatric surgery.

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

M. Gorry, T. Hart, E. Fıratlı, 2003, Journal of medical genetics.

Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.

M. Gorry, J. T. Wright, T. Hart, 2003, European journal of oral sciences.

Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

M. Gorry, G. Ehrlich, D. Whitcomb, 1996, Nature Genetics.

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1.

Mary L Marazita, M. Marazita, M. Gorry, 2002, American journal of human genetics.

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.

M. Gorry, Yingze Zhang, G. Ehrlich, 1997, Gastroenterology.

Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG)

M. Gorry, G. Ehrlich, D. Whitcomb, 1997, The American journal of gastroenterology.

Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients

M. Gorry, T. Hart, D. Tatakis, 2001, Journal of medical genetics.

Protection by deferoxamine from endothelial injury: a possible link with inhibition of intracellular xanthine oxidase.

M. Gorry, J. Rinaldo, 1990, American journal of respiratory cell and molecular biology.

Lack of R117H Mutation in the Cationic Trypsinogen Gene in Patients with Tropical Pancreatitis from Bangladesh

M. Gorry, G. Ehrlich, D. Whitcomb, 1998 .

Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh.

M. Gorry, G. Ehrlich, D. Whitcomb, 1998, Pancreas.

Evolution of human immunodeficiency virus type 1 envelope sequences in infected individuals with differing disease progression profiles.

G. Learn, A. Rodrigo, J. Mullins, 1998, Virology.

Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family.

M. Gorry, G. Ehrlich, Y. Zhang, 1999, Gene.

Oncolytic virotherapy for ovarian carcinomatosis using a replication-selective vaccinia virus armed with a yeast cytosine deaminase gene

S. Chalikonda, Xiao‐Yu Yin, H. Zeh, 2008, Cancer Gene Therapy.

High-dimensional profiling clusters asthma severity by lymphoid and non-lymphoid status

N. Aghaeepour, K. Nadeau, S. Wenzel, 2021, Cell reports.

Three Epigenetic Drugs Up-Regulate Homeobox Gene Rhox5 in Cancer Cells through Overlapping and Distinct Molecular Mechanisms

M. Gorry, Z. Guo, D. Bartlett, 2009, Molecular Pharmacology.

Effect of endotoxin-induced cell injury on 70-kD heat shock proteins in bovine lung endothelial cells.

M. Gorry, R. Abdolrasulnia, V. Shepherd, 1990, American journal of respiratory cell and molecular biology.

Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.

M. Gorry, T. Hart, J. Sandhu, 2003, Kidney international.

Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.

H. Losken, M. Gorry, G. Ehrlich, 1995, Human molecular genetics.

Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22→p21

M. Gorry, T. Hart, L. Wang, 2002, Cytogenetic and Genome Research.

Development of flow cytometry assays for measuring cell-membrane enzyme activity on individual cells

Michelle A. Garlin, Miles A. Miller, M. Gorry, 2020, Journal of Cancer.

ADAM10 Sheddase Activity is a Potential Lung-Cancer Biomarker

Miles A. Miller, D. Lauffenburger, L. Griffith, 2018, Journal of Cancer.

Modification of proteolytic activity matrix analysis (PrAMA) to measure ADAM10 and ADAM17 sheddase activities in cell and tissue lysates

Miles A. Miller, D. Lauffenburger, L. Griffith, 2017, Journal of Cancer.

Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene.

M. Gorry, H. Trachtman, T. Hart, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.