List of works - Péter Gergics

Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction.

scientific article

Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.

scientific article published on 19 July 2016

Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency

scientific article published in February 2018

Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

scientific article published on 9 November 2016

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

scientific article

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism

scientific article

ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons.

scientific article

Increased total scavenger capacity and decreased liver fat content in rats fed dehydroepiandrosterone and its sulphate on a high-fat diet

scientific article published on 28 September 2010

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

scientific article

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

scientific article published on 01 November 2007

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.

scientific article

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

scientific article published on 19 September 2005

Parathyroid hormone-dependent hypercalcemia.

scientific article published on January 2009

Pituitary gland development and disease: from stem cell to hormone production

scientific article

Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptine.

scientific article published in June 2005

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family

article

Serum chromogranin A reflects regression of metastatic carcinoid during prolonged octreotide treatment

The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome

scientific article published on 24 November 2010

The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model

scientific article

[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]

scientific article published on 01 October 2005

[Extracellular calcium sensing under normal and pathological conditions]

scientific article published on 01 April 2009

[Methods for the analysis of large gene deletions and their application in some hereditary diseases].

scientific article

[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].

scientific article

List of works by Péter Gergics

Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction.

Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.

Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency

Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism

ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons.

Increased total scavenger capacity and decreased liver fat content in rats fed dehydroepiandrosterone and its sulphate on a high-fat diet

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

Parathyroid hormone-dependent hypercalcemia.

Pituitary gland development and disease: from stem cell to hormone production

Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptine.

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family

Serum chromogranin A reflects regression of metastatic carcinoid during prolonged octreotide treatment

The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome

The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model

[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]

[Extracellular calcium sensing under normal and pathological conditions]

[Methods for the analysis of large gene deletions and their application in some hereditary diseases].

[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].