4.5 Article

SCARB1 downregulation in adrenal insufficiency with Allgrove syndrome

Related references

Note: Only part of the references are listed.
Review Neurosciences

Nucleo-cytoplasmic transport defects and protein aggregates in neurodegeneration

Giacomo Bitetto et al.

TRANSLATIONAL NEURODEGENERATION (2020)

Article Biochemistry & Molecular Biology

Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome

Giacomo Bitetto et al.

HUMAN MOLECULAR GENETICS (2019)

Article Endocrinology & Metabolism

Triple-A syndrome: a wide spectrum of adrenal dysfunction

Florence Roucher-Boulez et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY (2018)

Review Endocrinology & Metabolism

Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature

Hiren Patt et al.

ENDOCRINE CONNECTIONS (2017)

Review Endocrinology & Metabolism

ACTH Regulation of Adrenal SR-B1

Wen-Jun Shen et al.

FRONTIERS IN ENDOCRINOLOGY (2016)

Review Endocrinology & Metabolism

Impact of ACTH Signaling on Transcriptional Regulation of Steroidogenic Genes

Carmen Ruggiero et al.

FRONTIERS IN ENDOCRINOLOGY (2016)

Review Endocrinology & Metabolism

The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

Walter L. Miller et al.

ENDOCRINE REVIEWS (2011)

Article Endocrinology & Metabolism

Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2

Teng-Teng L. L. Chung et al.

CLINICAL ENDOCRINOLOGY (2010)

Article Multidisciplinary Sciences

The molecular architecture of the nuclear pore complex

Frank Alber et al.

NATURE (2007)

Review Endocrinology & Metabolism

Mechanisms of disease: the adrenocorticotropin receptor and disease

AJL Clark et al.

NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM (2006)

Article Multidisciplinary Sciences

ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome

M Hirano et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Review Endocrinology & Metabolism

Inherited ACTH insensitivity illuminates the mechanisms of ACTH action

AJL Clark et al.

TRENDS IN ENDOCRINOLOGY AND METABOLISM (2005)

Article Cell Biology

Androgen biosynthesis from cholesterol to DHEA

WL Miller

MOLECULAR AND CELLULAR ENDOCRINOLOGY (2002)

Article Cell Biology

Proteomic analysis of the mammalian nuclear pore complex

JA Cronshaw et al.

JOURNAL OF CELL BIOLOGY (2002)

Article Biochemistry & Molecular Biology

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene

K Handschug et al.

HUMAN MOLECULAR GENETICS (2001)

Article Genetics & Heredity

Mutant WD-repeat protein in triple-A syndrome

A Tullio-Pelet et al.

NATURE GENETICS (2000)