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COX7A2L/SCAFI and Pre-Complex III Modify Respiratory Chain Supercomplex Formation in Different Mouse Strains with a Bcs1l Mutation

PloS one, 2016-12, Vol.11 (12), p.e0168774-e0168774

2016

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Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency

PloS one, 2014-01, Vol.9 (1), p.e86767-e86767

2014

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Effect of High-Carbohydrate Diet on Plasma Metabolome in Mice with Mitochondrial Respiratory Chain Complex III Deficiency

International journal of molecular sciences, 2016-11, Vol.17 (11), p.1824-1824

2016

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Metabolite profiles reveal energy failure and impaired beta-oxidation in liver of mice with complex III deficiency due to a BCS1L mutation

PloS one, 2012-07, Vol.7 (7), p.e41156

2012

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A mouse model of mitochondrial complex III dysfunction induced by myxothiazol

Biochemical and biophysical research communications, 2014-04, Vol.446 (4), p.1079-1084

2014

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Mitochondrial hepatopathies in the newborn period

Seminars in fetal & neonatal medicine, 2011-08, Vol.16 (4), p.222-228

2011

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A mouse model of the GRACILE mutation Bsc1l A232G — Clues for another complex III assembly factor during early ontogenesis

Mitochondrion, 2011-07, Vol.11 (4), p.655-655

2011

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A role for the fibrinogen‐binding regions of streptococcal M proteins in phagocytosis resistance

Molecular microbiology, 2000-09, Vol.37 (6), p.1318-1326

2000

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The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: A viable mouse model for mitochondrial hepatopathy

Hepatology (Baltimore, Md.), 2011-02, Vol.53 (2), p.437-447

2011

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Kringle 2 Mediates High Affinity Binding of Plasminogen to an Internal Sequence in Streptococcal Surface Protein PAM

The Journal of biological chemistry, 1998-09, Vol.273 (38), p.24420-24424

1998

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Comparison of RNA‐ and DNA‐based methods for measurable residual disease analysis in NPM1‐mutated acute myeloid leukemia

International journal of laboratory hematology, 2021-08, Vol.43 (4), p.664-674

2021

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A novel role for constitutively expressed epithelial-derived chemokines as antibacterial peptides in the intestinal mucosa

Mucosal immunology, 2010-01, Vol.3 (1), p.40-48

2010

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Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice

Biochimica et biophysica acta. Molecular basis of disease, 2020-01, Vol.1866 (1), p.165573-165573, Article 165573

2020

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Mitochondrial disorders caused by mutations in respiratory chain assembly factors

Seminars in fetal & neonatal medicine, 2011-08, Vol.16 (4), p.197-204

2011

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Strain-Specific Restriction of the Antiphagocytic Property of Group A Streptococcal M Proteins

Infection and Immunity, 2000-01, Vol.68 (1), p.107-112

2000

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The radical-binding lipocalin A1M binds to a Complex I subunit and protects mitochondrial structure and function

Antioxidants & redox signaling, 2013-06, Vol.18 (16), p.2017-2028

2013

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A Turkish BCS1L mutation causes GRACILE-like disorder

Turkish journal of pediatrics, 2017, Vol.58 (6), p.658-661

2017

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Complex III staining in blue native polyacrylamide gels

Journal of inherited metabolic disease, 2011-06, Vol.34 (3), p.741-747

2011

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Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation

Mitochondrion, 2010-08, Vol.10 (5), p.497-509

2010

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The GRACILE Mutation Introduced into Bcs1I Causes Postnatal Complex III Deficiency: A Viable Mouse Model for Mitochondrial Hepatopathy

Hepatology (Baltimore, Md.), 2011, Vol.53 (2), p.437-447

2011

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90 Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis

Mitochondrion, 2010-03, Vol.10 (2), p.225

2010

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Role of the Hypervariable Region in Streptococcal M Proteins: Binding of a Human Complement Inhibitor

The Journal of immunology (1950), 1998-11, Vol.161 (9), p.4894-4901

1998

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Identification of a Domain in Human Factor H and Factor H-Like Protein-1 Required for the Interaction with Streptococcal M Proteins

The Journal of immunology (1950), 1998-04, Vol.160 (7), p.3349-3354

1998

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BCS1L is expressed in critical regions for neural development during ontogenesis in mice

Gene Expression Patterns, 2007-01, Vol.7 (3), p.266-273

2007

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Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis

Mitochondrion, 2010, Vol.10 (2), p.225

2010

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COX7A2L/SCAFI and Pre-Complex III Modify Respiratory Chain Supercomplex Formation in Different Mouse Strains with a Bcs1l Mutation

Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency

Effect of High-Carbohydrate Diet on Plasma Metabolome in Mice with Mitochondrial Respiratory Chain Complex III Deficiency

Metabolite profiles reveal energy failure and impaired beta-oxidation in liver of mice with complex III deficiency due to a BCS1L mutation

A mouse model of mitochondrial complex III dysfunction induced by myxothiazol

Mitochondrial hepatopathies in the newborn period

A mouse model of the GRACILE mutation Bsc1l A232G — Clues for another complex III assembly factor during early ontogenesis

A role for the fibrinogen‐binding regions of streptococcal M proteins in phagocytosis resistance

The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: A viable mouse model for mitochondrial hepatopathy

Kringle 2 Mediates High Affinity Binding of Plasminogen to an Internal Sequence in Streptococcal Surface Protein PAM

Comparison of RNA‐ and DNA‐based methods for measurable residual disease analysis in NPM1‐mutated acute myeloid leukemia

A novel role for constitutively expressed epithelial-derived chemokines as antibacterial peptides in the intestinal mucosa

Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice

Mitochondrial disorders caused by mutations in respiratory chain assembly factors

Strain-Specific Restriction of the Antiphagocytic Property of Group A Streptococcal M Proteins

The radical-binding lipocalin A1M binds to a Complex I subunit and protects mitochondrial structure and function

A Turkish BCS1L mutation causes GRACILE-like disorder

Complex III staining in blue native polyacrylamide gels

Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation

The GRACILE Mutation Introduced into Bcs1I Causes Postnatal Complex III Deficiency: A Viable Mouse Model for Mitochondrial Hepatopathy

90 Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis

Role of the Hypervariable Region in Streptococcal M Proteins: Binding of a Human Complement Inhibitor

Identification of a Domain in Human Factor H and Factor H-Like Protein-1 Required for the Interaction with Streptococcal M Proteins

BCS1L is expressed in critical regions for neural development during ontogenesis in mice

Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis

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