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The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

PloS one, 2011, Vol.6 (8), p.e24445-e24445

2011

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CFTR Cl − channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis

Gastroenterology (New York, N.Y. 1943), 2004-10, Vol.127 (4), p.1085-1095

2004

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Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia

Pediatric research, 2003-04, Vol.53 (4), p.608-618

2003

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Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes

British journal of pharmacology, 2000-08, Vol.130 (8), p.1884-1892

2000

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Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations

Human mutation, 2000-01, Vol.15 (1), p.115-116

2000

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Pediatric Reference Ranges for Osteocalcin Measured by the Immulite Analyzer

Clinical chemistry and laboratory medicine, 2001-10, Vol.39 (10), p.980-982

2001

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Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype

Pediatric research, 2000-09, Vol.48 (3), p.329-334

2000

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The ΔF508 mutation results in loss of CFTR function and mature protein in native human colon

Gastroenterology (New York, N.Y. 1943), 2004-01, Vol.126 (1), p.32-41

2004

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Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

Human genetics, 1997-09, Vol.100 (3-4), p.365-377

1997

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The K.sup.+ Channel Opener 1-EBIO Potentiates Residual Function of Mutant CFTR in Rectal Biopsies from Cystic Fibrosis Patients

PloS one, 2011-08, Vol.6 (8), p.e24445

2011

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INFLUENCE OF SIALIC ACID ON THE ADULT AND FETAL FIBRINOGEN-FIBRIN TRANSITION

Recent biochemical and medical aspects, 2019, Vol.1, p.91-100

Originally published 1982, 2019

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The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon

Gastroenterology (New York, N.Y. 1943), 2004-01, Vol.126 (1), p.32-41

2004

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Primary treatment of propionic acidemia complicated by acute thiamine deficiency

The Journal of pediatrics, 1996-11, Vol.129 (5), p.758-760

1996

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Isolation and complete amino‐acid sequence of the small polypeptide from light‐harvesting pigment‐protein complex I (B870) of Rhodopseudomonas capsulata

European journal of biochemistry, 1984-01, Vol.138 (1), p.209-212

1984

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Role of K V LQT1 in Cyclic Adenosine Monophosphate–Mediated Cl − Secretion in Human Airway Epithelia

American journal of respiratory cell and molecular biology, 2000-09, Vol.23 (3), p.283-289

2000

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Role of KVLQT1 in Cyclic Adenosine Monophosphate-Mediated Cl- Secretion in Human Airway Epithelia

American journal of respiratory cell and molecular biology, 2000-09, Vol.23 (3), p.283

2000

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Characterisation of calmodulin from Drosophila heads

Biochimica et biophysica acta, 1985-11, Vol.832 (2), p.228-232

1985

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Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case-control study

BMJ (Online), 2012-07, Vol.345, p.e4565

2012

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Glycogen storage disease type I: diagnosis and phenotype/genotype correlation

European journal of pediatrics, 2002-01, Vol.161, p.S10-S19

2002

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A novel missense mutation, S1159F, in exon 19 of the CFTR gene

Human mutation, 2000-04, Vol.15 (4), p.390-390

2000

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Expression of CNTF Receptor-{alpha} in Chick Violet-Sensitive Cones with Unique Morphologic Properties

Investigative ophthalmology & visual science, 2004-02, Vol.45 (2), p.655-661

2004

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A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene

Human mutation, 2000-09, Vol.16 (3), p.277-277

2000

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Kinetic Studies on a 4‐Methoxybenzoate O‐Demethylase from Pseudomonas putida

European journal of biochemistry, 1977-01, Vol.72 (1), p.107-115

1977

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The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

CFTR Cl − channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis

Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia

Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes

Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations

Pediatric Reference Ranges for Osteocalcin Measured by the Immulite Analyzer

Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype

The ΔF508 mutation results in loss of CFTR function and mature protein in native human colon

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

The K.sup.+ Channel Opener 1-EBIO Potentiates Residual Function of Mutant CFTR in Rectal Biopsies from Cystic Fibrosis Patients

INFLUENCE OF SIALIC ACID ON THE ADULT AND FETAL FIBRINOGEN-FIBRIN TRANSITION

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon

Primary treatment of propionic acidemia complicated by acute thiamine deficiency

Isolation and complete amino‐acid sequence of the small polypeptide from light‐harvesting pigment‐protein complex I (B870) of Rhodopseudomonas capsulata

Role of K V LQT1 in Cyclic Adenosine Monophosphate–Mediated Cl − Secretion in Human Airway Epithelia

Role of KVLQT1 in Cyclic Adenosine Monophosphate-Mediated Cl- Secretion in Human Airway Epithelia

Characterisation of calmodulin from Drosophila heads

Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case-control study

Glycogen storage disease type I: diagnosis and phenotype/genotype correlation

A novel missense mutation, S1159F, in exon 19 of the CFTR gene

Expression of CNTF Receptor-{alpha} in Chick Violet-Sensitive Cones with Unique Morphologic Properties

A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene

Kinetic Studies on a 4‐Methoxybenzoate O‐Demethylase from Pseudomonas putida

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