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

Journal of medical genetics, 2002-12, Vol.39 (12), p.882-892

2002

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

Journal of medical genetics, 2003-12, Vol.40 (12), p.900-906

2003

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

Nature genetics, 1996-10, Vol.14 (2), p.141-145

1996

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

Gastroenterology (New York, N.Y. 1943), 1997-10, Vol.113 (4), p.1063-1068

1997

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

JAMA : the journal of the American Medical Association, 1998-01, Vol.279 (4), p.296

1998

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

Cancer gene therapy, 2008-02, Vol.15 (2), p.115-125

2008

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

Genes and immunity, 2003-01, Vol.4 (1), p.22-29

2003

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Caution Ahead: Traffic Accidents in Cuba

MEDICC review, 2022-01, Vol.24 (1), p.77-77

Gorry, Conner

2022

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

Journal of medical genetics, 2001-02, Vol.38 (2), p.96-101

2001

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Aquaporin expression in developing human teeth and selected orofacial tissues

Calcified tissue international, 2003-03, Vol.72 (3), p.222-227

2003

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

Pancreas, 1998-10, Vol.17 (3), p.278-280

1998

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A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1

American journal of human genetics, 2002-04, Vol.70 (4), p.943-954

2002

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Structure and sequence of human FGF8

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.253-257

1996

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Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerations

Lancet neurology, 2015-08, Vol.14 (8), p.855-866

2015

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Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype

The American journal of gastroenterology, 1997-07, Vol.92 (7), p.1113-1116

1997

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

Gene, 1999-04, Vol.230 (1), p.69-79

1999

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Evolution of Human Immunodeficiency Virus Type 1 Envelope Sequences in Infected Individuals with Differing Disease Progression Profiles

Virology (New York, N.Y.), 1998-02, Vol.241 (2), p.251-259

1998

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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

Journal of pediatric surgery, 2000-03, Vol.35 (3), p.406-419

2000

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

Cytogenetic and genome research, 2001-01, Vol.95 (3-4), p.146-152

2001

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Cuba's Latin American Medical School: can socially-accountable medical education make a difference?

MEDICC review, 2012-07, Vol.14 (3), p.5-11

Gorry, Conner

2012

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CKDu ravages the Salvadoran countryside

MEDICC review, 2014-04, Vol.16 (2), p.5

Gorry, Conner

2014

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Aquaporin Expression in Developing Human Teeth and Selected Orofacial Tissues

Calcified tissue international, 2003-03, Vol.72 (3), p.222-227

2003

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Over the hills & far away: rural health in Cuba

MEDICC review, 2012-01, Vol.14 (1), p.6-10

Conner Gorry, MA

2012

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

American journal of respiratory cell and molecular biology, 1990-12, Vol.3 (6), p.525-533

1990

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Cuban maternity homes: a model to address at-risk pregnancy

MEDICC review, 2011-07, Vol.13 (3), p.12-15

Gorry, Conner

2011

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

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

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

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

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

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

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

Caution Ahead: Traffic Accidents in Cuba

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

Aquaporin expression in developing human teeth and selected orofacial tissues

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

A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1

Structure and sequence of human FGF8

Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerations

Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype

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

Evolution of Human Immunodeficiency Virus Type 1 Envelope Sequences in Infected Individuals with Differing Disease Progression Profiles

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

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

Cuba's Latin American Medical School: can socially-accountable medical education make a difference?

CKDu ravages the Salvadoran countryside

Aquaporin Expression in Developing Human Teeth and Selected Orofacial Tissues

Over the hills & far away: rural health in Cuba

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

Cuban maternity homes: a model to address at-risk pregnancy

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