Mobilities of complex glycosphingolipids in SDS gel electrophoresis

Recommendations for the classification of diseases as CFTR-related disorders.

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Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection.

Genes and immunity·2011

Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patients.

Journal of applied genetics·2010

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

Clinical genetics·2010

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society·2008

The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants.

Archives of disease in childhood·2005

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Acta haematologica Polonica·2020

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Acta haematologica Polonica·1996

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Acta haematologica Polonica·1996

Acute myelofibrosis in children: report on two cases.

Acta haematologica Polonica·1996

Pure but Not Simple: Supersaturation from Excipient-Free, Vapor-Generated, Amorphous Griseofulvin Nanoparticles.

Molecular pharmaceutics·2026

Systematic Investigation on Particle and Pore Size Effects of Mesoporous Silica on Molecular Mobility and Physical Stability of Overloaded Amorphous Acetaminophen.

Molecular pharmaceutics·2026

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Molecular pharmaceutics·2026

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ACS applied materials & interfaces·2026

Automated multimodal spectroscopy system for rapid microscope-free microplastic characterization.

Analytica chimica acta·2026

Loss of UBIQUITIN-PROTEIN LIGASE 3 (UPL3) impairs cellulose-xylan structural organization in Arabidopsis seed mucilage.

Plant physiology and biochemistry : PPB·2026

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Mobilities of complex glycosphingolipids in SDS gel electrophoresis

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Recommendations for the classification of diseases as CFTR-related disorders.

Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection.

Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patients.

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants.

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Acute myelofibrosis in children: report on two cases.

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Systematic Investigation on Particle and Pore Size Effects of Mesoporous Silica on Molecular Mobility and Physical Stability of Overloaded Amorphous Acetaminophen.

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Mobilities of complex glycosphingolipids in SDS gel electrophoresis

Abstract:

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