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From yeast to humans – roles of the Kennedy pathway for phosphatidylcholine synthesis

FEBS letters, 2018-04, Vol.592 (8), p.1256-1272

McMaster, Christopher R.

2018

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Genetic diseases of the Kennedy pathways for membrane synthesis

The Journal of biological chemistry, 2020-12, Vol.295 (51), p.17877-17886

2020

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Choline kinase inhibition promotes ER-phagy

Journal of lipid research, 2022-08, Vol.63 (8), p.100213-100213, Article 100213

2022

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Lipid synthesis and membrane contact sites: a crossroads for cellular physiology

Journal of lipid research, 2016-10, Vol.57 (10), p.1789-1805

2016

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The Mitochondrial Quality Control Protein Yme1 Is Necessary to Prevent Defective Mitophagy in a Yeast Model of Barth Syndrome

The Journal of biological chemistry, 2015-04, Vol.290 (14), p.9284-9298

2015

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Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia

PLoS genetics, 2016-01, Vol.12 (1), p.e1005783-e1005783

2016

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Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism

Nature communications, 2022-03, Vol.13 (1), p.1559-1559, Article 1559

2022

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Germline mutations in MAP3K6 are associated with familial gastric cancer

PLoS genetics, 2014-10, Vol.10 (10), p.e1004669-e1004669

2014

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Atrial natriuretic peptide signaling co-regulates lipid metabolism and ventricular conduction system gene expression in the embryonic heart

iScience, 2024-01, Vol.27 (1), p.108748-108748, Article 108748

2024

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Phospholipid Transfer Protein Sec14 Is Required for Trafficking from Endosomes and Regulates Distinct trans-Golgi Export Pathways

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.7364-7375

2009

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oxysterol binding protein Kes1p regulates Golgi apparatus phosphatidylinositol-4-phosphate function

Proceedings of the National Academy of Sciences - PNAS, 2007-09, Vol.104 (39), p.15352-15357

2007

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Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review

American journal of ophthalmology case reports, 2024-06, Vol.34, p.102051, Article 102051

2024

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Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy

PloS one, 2016-08, Vol.11 (8), p.e0158320

2016

Volltextzugriff (PDF)

Vesicle-associated Membrane Protein-associated Protein-A (VAP-A) Interacts with the Oxysterol-binding Protein to Modify Export from the Endoplasmic Reticulum

The Journal of biological chemistry, 2002-08, Vol.277 (33), p.29908-29918

2002

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Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations

Frontiers in pediatrics, 2020-12, Vol.8, p.579924-579924

2020

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Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia

Pediatric blood & cancer, 2016-07, Vol.63 (7), p.1307-1309

2016

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The major sites of cellular phospholipid synthesis and molecular determinants of Fatty Acid and lipid head group specificity

Molecular biology of the cell, 2002-09, Vol.13 (9), p.3148-3161

2002

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The leucine zipper domain of the transcriptional repressor Opi1 underlies a signal transduction mechanism regulating lipid synthesis

The Journal of biological chemistry, 2023-12, Vol.299 (12), p.105417-105417, Article 105417

2023

Volltextzugriff (PDF)

A Chemogenomic Screen in Saccharomyces cerevisiae Uncovers a Primary Role for the Mitochondria in Farnesol Toxicity and Its Regulation by the Pkc1 Pathway

The Journal of biological chemistry, 2007-02, Vol.282 (7), p.4868-4874

2007

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A generalizable pre-clinical research approach for orphan disease therapy

Orphanet journal of rare diseases, 2012-06, Vol.7 (1), p.39-39, Article 39

2012

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The yeast oxysterol binding protein Kes1 maintains sphingolipid levels

PloS one, 2013-04, Vol.8 (4), p.e60485-e60485

2013

Volltextzugriff (PDF)

Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14

PloS one, 2013-01, Vol.8 (1), p.e55388

2013

Volltextzugriff (PDF)

Glycerophosphocholine Catabolism as a New Route for Choline Formation for Phosphatidylcholine Synthesis by the Kennedy Pathway

The Journal of biological chemistry, 2005-11, Vol.280 (46), p.38290-38296

2005

Volltextzugriff (PDF)

Defects in integrin complex formation promote CHKB -mediated muscular dystrophy

Life science alliance, 2024-08, Vol.7 (8), p.e202301956

2024

Volltextzugriff (PDF)

A novel rearrangement of occludin causes brain calcification and renal dysfunction

Human genetics, 2013-11, Vol.132 (11), p.1223-1234

2013

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From yeast to humans – roles of the Kennedy pathway for phosphatidylcholine synthesis

Genetic diseases of the Kennedy pathways for membrane synthesis

Choline kinase inhibition promotes ER-phagy

Lipid synthesis and membrane contact sites: a crossroads for cellular physiology

The Mitochondrial Quality Control Protein Yme1 Is Necessary to Prevent Defective Mitophagy in a Yeast Model of Barth Syndrome

Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia

Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism

Germline mutations in MAP3K6 are associated with familial gastric cancer

Atrial natriuretic peptide signaling co-regulates lipid metabolism and ventricular conduction system gene expression in the embryonic heart

Phospholipid Transfer Protein Sec14 Is Required for Trafficking from Endosomes and Regulates Distinct trans-Golgi Export Pathways

oxysterol binding protein Kes1p regulates Golgi apparatus phosphatidylinositol-4-phosphate function

Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review

Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy

Vesicle-associated Membrane Protein-associated Protein-A (VAP-A) Interacts with the Oxysterol-binding Protein to Modify Export from the Endoplasmic Reticulum

Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations

Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia

The major sites of cellular phospholipid synthesis and molecular determinants of Fatty Acid and lipid head group specificity

The leucine zipper domain of the transcriptional repressor Opi1 underlies a signal transduction mechanism regulating lipid synthesis

A Chemogenomic Screen in Saccharomyces cerevisiae Uncovers a Primary Role for the Mitochondria in Farnesol Toxicity and Its Regulation by the Pkc1 Pathway

A generalizable pre-clinical research approach for orphan disease therapy

The yeast oxysterol binding protein Kes1 maintains sphingolipid levels

Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14

Glycerophosphocholine Catabolism as a New Route for Choline Formation for Phosphatidylcholine Synthesis by the Kennedy Pathway

Defects in integrin complex formation promote CHKB -mediated muscular dystrophy

A novel rearrangement of occludin causes brain calcification and renal dysfunction

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