Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c (Q24292254)

Holocytochrome c synthetase

GOA release 2020-03-11

1 reference

MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome

GOA release 2020-03-11

author

Quenten P. Schwarz

series ordinal

1

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author name string

Timothy C Cox

series ordinal

2

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language of work or name

English

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publication date

January 2002

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published in

Genomics

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volume

79

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page(s)

51-7

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issue

1

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cites work

1 reference

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Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

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Identification and sequence of the gene encoding cytochrome c heme lyase in the yeast Saccharomyces cerevisiae

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Selection of chromosome 22-specific clones from human genomic BAC library using a chromosome-specific cosmid library pool

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Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS)

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Isolation and characterization of a mouse homolog of the X-linked ocular albinism (OA1) gene.

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Cloning and characterization of a novel rho-type GTPase-activating protein gene (ARHGAP6) from the critical region for microphthalmia with linear skin defects

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Structure and expression of the gene encoding mouse F-box protein, Fwd2.

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c

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Evolutionary rate of a gene affected by chromosomal position.

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Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

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A very high density microsatellite map (1 STR/41 kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical region

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7 January 2021

Molecular cloning and characterization of a Candida albicans gene coding for cytochrome c haem lyase and a cell wall-related protein

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7 January 2021

Heme binding to a conserved Cys-Pro-Val motif is crucial for the catalytic function of mitochondrial heme lyases

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Cytochrome c heme lyase activity of yeast mitochondria.

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Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

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Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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7 January 2021

Mitochondrial diseases in man and mouse

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Role of cytochrome c heme lyase in mitochondrial import and accumulation of cytochrome c in Saccharomyces cerevisiae

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Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS).

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Splicing of messenger RNA precursors

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