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WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating

Nature genetics, 2019-12, Vol.51 (12), p.1723-1731

2019

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Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1997, Vol.82 (1), p.194-199

1997

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Author Correction: WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating

Nature genetics, 2020-11, Vol.52 (11), p.1265-1265

2020

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Expression pattern of the PRDX2, RAB1A, RAB1B, RAB5A and RAB25 genes in normal and cancer cervical tissues

International journal of oncology, 2015-01, Vol.46 (1), p.107-112

2015

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Opioid neuropeptide genotypes in relation to heroin abuse: Dopamine tone contributes to reversed mesolimbic proenkephalin expression

Proceedings of the National Academy of Sciences - PNAS, 2008-01, Vol.105 (2), p.786-791

2008

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21‐hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison's disease

Clinical and experimental immunology, 1997-02, Vol.107 (2), p.341-346

1997

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μ Opioid Receptor A118G Polymorphism in Association with Striatal Opioid Neuropeptide Gene Expression in Heroin Abusers

Proceedings of the National Academy of Sciences - PNAS, 2006-05, Vol.103 (20), p.7883-7888

2006

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Stability of mitochondrial DNA against reactive oxygen species (ROS) generated in diabetes

Diabetes/metabolism research and reviews, 2011-07, Vol.27 (5), p.470-479

2011

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Epigenetic DNA methylation in the promoters of the Igf1 receptor and insulin receptor genes in db/db mice

Epigenetics, 2011-04, Vol.6 (4), p.405-409

2011

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Effects of a low-intensity electromagnetic field on fibroblast migration and proliferation

Electromagnetic biology and medicine, 2011-06, Vol.30 (2), p.80-85

2011

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Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats

Human molecular genetics, 2000-09, Vol.9 (14), p.2149-2158

2000

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Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats

Human molecular genetics, 2000-09, Vol.9 (14), p.2149-2158

2000

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Prodynorphin transcripts and proteins differentially expressed and regulated in the adult human brain

The FASEB journal, 2005-09, Vol.19 (11), p.1543-1545

2005

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p53 splice variants generated by atypical mRNA processing confer complexity of p53 transcripts in the human brain

Biochemical and biophysical research communications, 2006-12, Vol.351 (2), p.383-386

2006

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High diagnostic accuracy for idiopathic Addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase

The journal of clinical endocrinology and metabolism, 1995, Vol.80 (9), p.2752-2755

1995

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High diagnostic accuracy for idiopathic addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase

The journal of clinical endocrinology and metabolism, 1995-09, Vol.80 (9), p.2752-2755

1995

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A New Locus for Autosomal Recessive Hypercholesterolemia Maps to Human Chromosome 15q25-q26

American journal of human genetics, 2000-02, Vol.66 (2), p.453-460

2000

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A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

Human genetics, 1997-06, Vol.99 (6), p.704-709

1997

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A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility

Clinical endocrinology (Oxford), 2001-06, Vol.54 (6), p.827-834

2001

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Naturally Occurring Mutants of Human Steroid 21-Hydroxylase (P450c21) Pinpoint Residues Important for Enzyme Activity and Stability

The Journal of biological chemistry, 1998-03, Vol.273 (11), p.6163-6165

1998

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Effects of Missense Mutations and Deletions on Membrane Anchoring and Enzyme Function of Human Steroid 21-Hydroxylase (P450c21)

Biochemical and biophysical research communications, 1999-04, Vol.257 (2), p.384-390

1999

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A Conformation-Dependent Epitope in Addison's Disease and Other Endocrinological Autoimmune Diseases Maps to a Carboxyl-Terminal Functional Domain of Human Steroid 21-Hydroxylase

The Journal of immunology (1950), 1999-02, Vol.162 (4), p.2422-2426

1999

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Structure and Transcription Regulation of the Human Insulin-like Growth Factor Binding Protein 4 Gene (IGFBP4)

Genomics (San Diego, Calif.), 1998-05, Vol.49 (3), p.401-410

1998

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Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor

Hormone research, 2000-01, Vol.53 (2), p.83-88

2000

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Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome

Human genetics, 1998-10, Vol.103 (4), p.529-531

1998

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WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating

Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiency

Author Correction: WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating

Expression pattern of the PRDX2, RAB1A, RAB1B, RAB5A and RAB25 genes in normal and cancer cervical tissues

Opioid neuropeptide genotypes in relation to heroin abuse: Dopamine tone contributes to reversed mesolimbic proenkephalin expression

21‐hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison's disease

μ Opioid Receptor A118G Polymorphism in Association with Striatal Opioid Neuropeptide Gene Expression in Heroin Abusers

Stability of mitochondrial DNA against reactive oxygen species (ROS) generated in diabetes

Epigenetic DNA methylation in the promoters of the Igf1 receptor and insulin receptor genes in db/db mice

Effects of a low-intensity electromagnetic field on fibroblast migration and proliferation

Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats

Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats

Prodynorphin transcripts and proteins differentially expressed and regulated in the adult human brain

p53 splice variants generated by atypical mRNA processing confer complexity of p53 transcripts in the human brain

High diagnostic accuracy for idiopathic Addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase

High diagnostic accuracy for idiopathic addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase

A New Locus for Autosomal Recessive Hypercholesterolemia Maps to Human Chromosome 15q25-q26

A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility

Naturally Occurring Mutants of Human Steroid 21-Hydroxylase (P450c21) Pinpoint Residues Important for Enzyme Activity and Stability

Effects of Missense Mutations and Deletions on Membrane Anchoring and Enzyme Function of Human Steroid 21-Hydroxylase (P450c21)

A Conformation-Dependent Epitope in Addison's Disease and Other Endocrinological Autoimmune Diseases Maps to a Carboxyl-Terminal Functional Domain of Human Steroid 21-Hydroxylase

Structure and Transcription Regulation of the Human Insulin-like Growth Factor Binding Protein 4 Gene (IGFBP4)

Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome

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