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Clinical evidence that V456A is a Cystic Fibrosis causing mutation in South Asians

Journal of cystic fibrosis, 2012-07, Vol.11 (4), p.312-315

2012

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Cystic Fibrosis (CF), Pseudomonas aeruginosa, CFTR and the CF Glycosylation Phenotype: A Review and Update

Current organic chemistry, 2008-07, Vol.12 (11), p.900-910

2008

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Coordinate induction of two antibiotic genes in tracheal epithelial cells exposed to the inflammatory mediators lipopolysaccharide and tumor necrosis factor alpha

Infection and Immunity, 1996-05, Vol.64 (5), p.1565-1568

1996

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Prospective evaluation of growth, nutritional status, and body composition in children with cystic fibrosis

The American journal of clinical nutrition, 2000-08, Vol.72 (2), p.407-413

2000

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Longitudinal, prospective analysis of dietary intake in children with cystic fibrosis

The Journal of pediatrics, 1996-07, Vol.129 (1), p.119-129

1996

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Terminal glycosylation in cystic fibrosis

BBA - Molecular Basis of Disease, 1999-10, Vol.1455 (2), p.241-253

1999

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Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis

Pediatric research, 1996-10, Vol.40 (4), p.578-586

1996

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Nuclear Translocation of Lactosylated Poly-l-lysine/cDNA Complex in Cystic Fibrosis Airway Epithelial Cells

Molecular therapy, 2001-06, Vol.3 (6), p.831-841

2001

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Sustainable Protein Sources: Advances for a Healthier Tomorrow

Second edition, 2023

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The Glycobiology of Cystic Fibrosis

Current organic chemistry, 2004-03, Vol.8 (5), p.385-394

2004

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Acute pulmonary exacerbation is not associated with increased energy expenditure in children with cystic fibrosis

The Journal of pediatrics, 1998-03, Vol.132 (3), p.493-499

1998

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A cross-species analysis of the cystic fibrosis transmembrane conductance regulator. Potential functional domains and regulatory sites

The Journal of biological chemistry, 1991-11, Vol.266 (33), p.22761-22769

1991

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Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells

Biochimie, 2001-08, Vol.83 (8), p.743-747

2001

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Energy expenditure and genotype of children with cystic fibrosis

Pediatric research, 1994-04, Vol.35 (4), p.451-460

1994

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Dietary intake of healthy children with cystic fibrosis compared with normal control children

Pediatrics (Evanston), 1992-10, Vol.90 (4), p.547-553

1992

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Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell

Glycoconjugate journal, 2001-09, Vol.18 (9), p.649-659

2001

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Terminal glycosylation and disease: influence on cancer and cystic fibrosis

Glycoconjugate journal, 2000-07, Vol.17 (7-9), p.617-626

2000

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Purification and characterization of GDP-L-fucose-N-acetyl beta-D-glucosaminide alpha 1----6fucosyltransferase from cultured human skin fibroblasts. Requirement of a specific biantennary oligosaccharide as substrate

The Journal of biological chemistry, 1991-11, Vol.266 (32), p.21572-21577

1991

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Management and survival of meconium ileus : a 30-year review

Annals of surgery, 1992-02, Vol.215 (2), p.179-185

1992

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Glycosylation and the cystic fibrosis transmembrane conductance regulator

Respiratory research, 2001-01, Vol.2 (5), p.276-279, Article 276

2001

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Body composition of children with cystic fibrosis with mild clinical manifestations compared with normal children

The American journal of clinical nutrition, 1994-01, Vol.59 (1), p.123-128

1994

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Gene therapy of cystic fibrosis (CF) airways: a review emphasizing targeting with lactose

Glycoconjugate journal, 2001-09, Vol.18 (9), p.731-740

2001

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Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells

Human gene therapy, 1996-08, Vol.7 (13), p.1577-1586

1996

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Enhanced Efficiency of Lactosylated Poly-L-Lysine-Mediated Gene Transfer into Cystic Fibrosis Airway Epithelial Cells

American journal of respiratory cell and molecular biology, 1999-05, Vol.20 (5), p.1081-1086

1999

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High-efficiency transfer of cystic fibrosis transmembrane conductance regulator cDNA into cystic fibrosis airway cells in culture using lactosylated polylysine as a vector

Human gene therapy, 1999-03, Vol.10 (4), p.615-622

1999

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Clinical evidence that V456A is a Cystic Fibrosis causing mutation in South Asians

Cystic Fibrosis (CF), Pseudomonas aeruginosa, CFTR and the CF Glycosylation Phenotype: A Review and Update

Coordinate induction of two antibiotic genes in tracheal epithelial cells exposed to the inflammatory mediators lipopolysaccharide and tumor necrosis factor alpha

Prospective evaluation of growth, nutritional status, and body composition in children with cystic fibrosis

Longitudinal, prospective analysis of dietary intake in children with cystic fibrosis

Terminal glycosylation in cystic fibrosis

Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis

Nuclear Translocation of Lactosylated Poly-l-lysine/cDNA Complex in Cystic Fibrosis Airway Epithelial Cells

Sustainable Protein Sources: Advances for a Healthier Tomorrow

The Glycobiology of Cystic Fibrosis

Acute pulmonary exacerbation is not associated with increased energy expenditure in children with cystic fibrosis

A cross-species analysis of the cystic fibrosis transmembrane conductance regulator. Potential functional domains and regulatory sites

Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells

Energy expenditure and genotype of children with cystic fibrosis

Dietary intake of healthy children with cystic fibrosis compared with normal control children

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell

Terminal glycosylation and disease: influence on cancer and cystic fibrosis

Purification and characterization of GDP-L-fucose-N-acetyl beta-D-glucosaminide alpha 1----6fucosyltransferase from cultured human skin fibroblasts. Requirement of a specific biantennary oligosaccharide as substrate

Management and survival of meconium ileus : a 30-year review

Glycosylation and the cystic fibrosis transmembrane conductance regulator

Body composition of children with cystic fibrosis with mild clinical manifestations compared with normal children

Gene therapy of cystic fibrosis (CF) airways: a review emphasizing targeting with lactose

Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells

Enhanced Efficiency of Lactosylated Poly-L-Lysine-Mediated Gene Transfer into Cystic Fibrosis Airway Epithelial Cells

High-efficiency transfer of cystic fibrosis transmembrane conductance regulator cDNA into cystic fibrosis airway cells in culture using lactosylated polylysine as a vector

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