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Relation between Mutations of the Cystic Fibrosis Gene and Idiopathic Pancreatitis

The New England journal of medicine, 1998-09, Vol.339 (10), p.653-658

1998

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Associations of childhood maltreatment with binge eating and binge drinking in emerging adult women

Preventive medicine reports, 2023-06, Vol.33, p.102217-102217, Article 102217

2023

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Treatment of minocycline-induced cutaneous pigmentation with the Q-switched Alexandrite laser and a review of the literature

Journal of the American Academy of Dermatology, 2001-02, Vol.44 (2), p.342-347

2001

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Intermittent hypoxia-induced increases in reactive oxygen species activate NFATc3 increasing endothelin-1 vasoconstrictor reactivity

Vascular pharmacology, 2014-01, Vol.60 (1), p.17-24

2014

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A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

The New England journal of medicine, 1994-10, Vol.331 (15), p.974-980

1994

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Lower serum ceruloplasmin levels correlate with younger age of onset in Parkinson’s disease

Journal of neurology, 2008-12, Vol.255 (12), p.1957-1962

2008

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Lung disease associated with the IVS8 5T allele of the CFTR gene

American journal of respiratory and critical care medicine, 2000-11, Vol.162 (5), p.1919-1924

2000

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Availability of wild spat of the blacklip pearl oyster, Pinctada margaritifera, from `open' reef systems in Solomon Islands

Aquaculture, 1998-09, Vol.167 (3), p.283-299

1998

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Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75

American journal of human genetics, 1997-05, Vol.60 (5), p.1122-1127

1997

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A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides

Clinical genetics, 2005-07, Vol.68 (1), p.88-90

2005

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Correction of Aberrant Splicing of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene by Antisense Oligonucleotides

The Journal of biological chemistry, 1999-12, Vol.274 (51), p.36193-36199

1999

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Shorter immersion times increase yields of the blacklip pearl oyster, Pinctada margaritifera (Linne.), from spat collectors in Solomon Islands

Aquaculture, 2000-07, Vol.187 (3), p.299-313

2000

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Cystic fibrosis syndrome: a new paradigm for inherited disorders and implications for molecular diagnostics

Clinical chemistry (Baltimore, Md.), 1999-07, Vol.45 (7), p.929-931

1999

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Variation in abundance of blacklip pearl oyster ( Pinctada margaritifera Linne.) spat from inshore and offshore reefs in Solomon Islands

Aquaculture, 1999-08, Vol.178 (3), p.273-291

1999

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Marine species conservation at CITES: How does media coverage inform or misinform?

Marine policy, 2021-12, Vol.134, p.104813, Article 104813

2021

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Complete deletion of the androgen receptor gene : definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status

The journal of clinical endocrinology and metabolism, 1992-04, Vol.74 (4), p.927-933

1992

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Cystic Fibrosis Transmembrane-Conductance Regulator Mutations among African Americans

American journal of human genetics, 1998-01, Vol.62 (1), p.195-196

1998

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Detecting multiple cystic fibrosis mutations by polymerase chain reaction-mediated site-directed mutagenesis

Clinical chemistry (Baltimore, Md.), 1991-05, Vol.37 (5), p.753

1991

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Low-grade primary cutaneous adenosquamous (mucoepidermoid) carcinoma: report of a case and review of the literature

The American journal of dermatopathology, 1989, Vol.11 (1), p.43-50

FRIEDMAN, K. J

1989

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Association of pancreatic adenocarcinoma, mild lung disease, and delta F508 mutation in a cystic fibrosis patient

Clinical chemistry (Baltimore, Md.), 1994-10, Vol.40 (10), p.1972

1994

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Screening Young syndrome patients for CFTR mutations

American journal of respiratory and critical care medicine, 1995-10, Vol.152 (4 Pt 1), p.1353

1995

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Therapy of Chronic Graft-v-Host Disease in a Rat Model

Blood, 1989-07, Vol.74 (1), p.507-511

1989

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Cystic fibrosis deletion mutation detected by PCR-mediated site-directed mutagenesis

Clinical chemistry (Baltimore, Md.), 1990-04, Vol.36 (4), p.695

1990

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Urticaria Pigmentosa and Juvenile Xanthogranuloma: Case Report and Brief Review of the Literature

Pediatric dermatology, 1996-03, Vol.13 (2), p.122-126

1996

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Direct detection of mutations in the breast and ovarian cancer susceptibility gene BRCA1 by PCR-mediated site-directed mutagenesis

Clinical chemistry (Baltimore, Md.), 1997-01, Vol.43 (1), p.24-29

1997

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Relation between Mutations of the Cystic Fibrosis Gene and Idiopathic Pancreatitis

Associations of childhood maltreatment with binge eating and binge drinking in emerging adult women

Treatment of minocycline-induced cutaneous pigmentation with the Q-switched Alexandrite laser and a review of the literature

Intermittent hypoxia-induced increases in reactive oxygen species activate NFATc3 increasing endothelin-1 vasoconstrictor reactivity

A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

Lower serum ceruloplasmin levels correlate with younger age of onset in Parkinson’s disease

Lung disease associated with the IVS8 5T allele of the CFTR gene

Availability of wild spat of the blacklip pearl oyster, Pinctada margaritifera, from `open' reef systems in Solomon Islands

Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75

A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides

Correction of Aberrant Splicing of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene by Antisense Oligonucleotides

Shorter immersion times increase yields of the blacklip pearl oyster, Pinctada margaritifera (Linne.), from spat collectors in Solomon Islands

Cystic fibrosis syndrome: a new paradigm for inherited disorders and implications for molecular diagnostics

Variation in abundance of blacklip pearl oyster ( Pinctada margaritifera Linne.) spat from inshore and offshore reefs in Solomon Islands

Marine species conservation at CITES: How does media coverage inform or misinform?

Complete deletion of the androgen receptor gene : definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status

Cystic Fibrosis Transmembrane-Conductance Regulator Mutations among African Americans

Detecting multiple cystic fibrosis mutations by polymerase chain reaction-mediated site-directed mutagenesis

Low-grade primary cutaneous adenosquamous (mucoepidermoid) carcinoma: report of a case and review of the literature

Association of pancreatic adenocarcinoma, mild lung disease, and delta F508 mutation in a cystic fibrosis patient

Screening Young syndrome patients for CFTR mutations

Therapy of Chronic Graft-v-Host Disease in a Rat Model

Cystic fibrosis deletion mutation detected by PCR-mediated site-directed mutagenesis

Urticaria Pigmentosa and Juvenile Xanthogranuloma: Case Report and Brief Review of the Literature

Direct detection of mutations in the breast and ovarian cancer susceptibility gene BRCA1 by PCR-mediated site-directed mutagenesis

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