P. Gergics

发表

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

S. Camper, R. Reeves, Huiqing Li, 2015, BMC Developmental Biology.

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

Ryan E. Mills, J. Kitzman, Jun Z. Li, 2016, Endocrine reviews.

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

B. Ellsworth, S. Camper, M. Brinkmeier, 2013, Current topics in developmental biology.

The phenotypic spectrum associated with OTX2 mutations in humans

Jun Z. Li, M. Maghnie, M. Dattani, 2021, European journal of endocrinology.

[Extracellular calcium sensing under normal and pathological conditions].

Z. Tulassay, K. Rácz, M. Tóth, 2009, Orvosi hetilap.

Murine SEC24D can substitute functionally for SEC24C during embryonic development

K. Tomberg, M. Hoenerhoff, A. Kiseleva, 2021, Scientific Reports.

Murine SEC24D Can Substitute Functionally for SEC24C in vivo

K. Tomberg, A. Kiseleva, D. Ginsburg, 2018, bioRxiv.

otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.

S. Camper, J. Shavit, Brenda L. Bohnsack, 2020, Human molecular genetics.

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

M. Tóth, A. Patócs, G. Czirják, 2007, Clinical endocrinology.

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

P. Igaz, Z. Tulassay, K. Rácz, 2009, European journal of gastroenterology & hepatology.

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

K. Rácz, M. Tóth, A. Patócs, 2011, The Journal of Steroid Biochemistry and Molecular Biology.

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism.

S. Camper, A. Hollenberg, M. Brinkmeier, 2015, Molecular endocrinology.

Parathyroid hormone-dependent hypercalcemia

K. Rácz, M. Tóth, A. Patócs, 2009, Wiener klinische Wochenschrift.

Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases

K. Rácz, G. Fekete, P. Gergics, 2008, European Journal of Pediatrics.

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

L. Hunyady, K. Rácz, M. Tóth, 2007, Clinical endocrinology.

Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancer

P. Igaz, A. Tordai, K. Rácz, 2006, Wiener klinische Wochenschrift.

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

K. Rácz, M. Tóth, A. Patócs, 2006, The Journal of Steroid Biochemistry and Molecular Biology.

Overrepresentation of the N363S variant of the glucocorticoid receptor gene in patients with bilateral adrenal incidentalomas.

K. Rácz, M. Tóth, A. Patócs, 2006, The Journal of clinical endocrinology and metabolism.

Increased Total Scavenger Capacity and Decreased Liver Fat Content in Rats Fed Dehydroepiandrosterone and Its Sulphate on a High-Fat Diet

J. Féher, Z. Tulassay, K. Rácz, 2010, Gerontology.

Pituitary Transcription Factor Mutations Leading to Hypopituitarism.

P. Gergics, Péter Gergics, 2019, Experientia supplementum.

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

H. Christian, S. Camper, P. Gergics, 2016, Endocrinology.

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

P. Barsi, S. Czirják, K. Rácz, 2005, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

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

P. Igaz, K. Rácz, M. Tóth, 2009, Orvosi hetilap.

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

Hae-Chul Park, Namhee Kim, Hojae Lee, 2016, Scientific Reports.

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

K. Rácz, M. Tóth, A. Patócs, 2008, BMC Medical Genetics.

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

S. Camper, M. Brinkmeier, P. Gergics, 2015, Molecular endocrinology.

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

P. Igaz, K. Rácz, M. Tóth, 2009, European journal of endocrinology.

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

Michael H. Guo, J. Kitzman, Jun Z. Li, 2021, medRxiv.

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

K. Rácz, M. Tóth, I. Varga, 2005, The Journal of Steroid Biochemistry and Molecular Biology.

Polymorphisms of the ApoE, HSD3B1, IL-1beta and p53 genes are associated with the development of early uremic complications in diabetic patients: results of a DNA resequencing array study.

Zsolt Tulassay, Orsolya Galamb, Béla Molnár, 2009, International journal of molecular medicine.

Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

Jun Z. Li, S. Camper, B. Mendonca, 2023, Endocrine connections.

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

P. Igaz, Z. Tulassay, K. Rácz, 2009, European journal of gastroenterology & hepatology.