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The Effect of Gene Editing by CRISPR-Cas9 of miR-21 and the Indirect Target MMP9 in Metastatic Prostate Cancer

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14847

2023

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Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil

Pituitary, 2021-04, Vol.24 (2), p.252-261

2021

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ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome

Endocrine Connections, 2019-11, Vol.8 (11), p.1513-1519

2019

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Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

Fertility and sterility, 2013-09, Vol.100 (3), p.854-859

2013

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A GPR54-Activating Mutation in a Patient with Central Precocious Puberty

The New England journal of medicine, 2008-02, Vol.358 (7), p.709-715

2008

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Impaired Bone Microarchitecture in Premenopausal Women With Acromegaly: The Possible Role of Wnt Signaling

The journal of clinical endocrinology and metabolism, 2021-09, Vol.106 (9), p.2690-2706

2021

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Survivin: A Potential Marker of Resistance to Somatostatin Receptor Ligands

The journal of clinical endocrinology and metabolism, 2023-04, Vol.108 (4), p.876-887

2023

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Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren

Jornal de pediatria, 2014-09, Vol.90 (5), p.500-505

2014

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GH-Releasing Hormone Receptor Gene: A Novel Splice-Disrupting Mutation and Study of Founder Effects

Hormone research in paediatrics, 2012-01, Vol.78 (3), p.165-172

2012

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Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients

Journal of endocrinology, 2005-12, Vol.187 (3), p.361-368

2005

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Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

The journal of clinical endocrinology and metabolism, 2010-07, Vol.95 (7), p.3491-3496

2010

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Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies

Asian journal of andrology, 2011-03, Vol.13 (2), p.203-204

Trarbach, Ericka B

2011

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Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism

The journal of clinical endocrinology and metabolism, 2014-09, Vol.99 (9), p.E1808-E1813

2014

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Differential gene expression of sirtuins between somatotropinomas and nonfunctioning pituitary adenomas

Pituitary, 2018-08, Vol.21 (4), p.355-361

2018

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Association between KISS1 rs5780218 promoter polymorphism and onset of growth hormone secreting pituitary adenoma

Annales d'endocrinologie, 2019-04, Vol.80 (2), p.96-100

2019

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SOCS2 polymorphisms are not associated with clinical and biochemical phenotypes in acromegalic patients

Pituitary, 2017-06, Vol.20 (3), p.319-324

2017

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New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

Journal of the Endocrine Society, 2019-09, Vol.3 (9), p.1682-1692

2019

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Influence of growth hormone receptor (GHR) exon 3 and -202A/C IGFBP-3 genetic polymorphisms on clinical and biochemical features and therapeutic outcome of patients with acromegaly

Pituitary, 2015-10, Vol.18 (5), p.666-673

2015

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The Interactive Effect of GHR-Exon 3 and −202 A/C IGFBP3 Polymorphisms on rhGH Responsiveness and Treatment Outcomes in Patients with Turner Syndrome

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.E671-E677

2012

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FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

Endocrine Connections, 2015-06, Vol.4 (2), p.100-107

2015

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Evaluation of Downstream Regulatory Element Antagonistic Modulator Gene in Human Multinodular Goiter

Medical science monitor. Basic research, 2015-08, Vol.21, p.179-182

2015

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Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Endocrine reviews, 2010-06, Vol.31 (3), p.397-397

2010

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Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren

Jornal de Pediatria (Versão em Português), 2014-09, Vol.90 (5), p.500-505

2014

Volltextzugriff (PDF)

Copy number variation associated with Kallmann syndrome： new genetics insights from genome-wide studies

Asian journal of andrology, 2011, Vol.13 (2), p.205-206

Ericka B Trarbach

2011

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The Effect of Gene Editing by CRISPR-Cas9 of miR-21 and the Indirect Target MMP9 in Metastatic Prostate Cancer

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay

Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome

Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

A GPR54-Activating Mutation in a Patient with Central Precocious Puberty

Impaired Bone Microarchitecture in Premenopausal Women With Acromegaly: The Possible Role of Wnt Signaling

Survivin: A Potential Marker of Resistance to Somatostatin Receptor Ligands

Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren

GH-Releasing Hormone Receptor Gene: A Novel Splice-Disrupting Mutation and Study of Founder Effects

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies

Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism

Differential gene expression of sirtuins between somatotropinomas and nonfunctioning pituitary adenomas

Association between KISS1 rs5780218 promoter polymorphism and onset of growth hormone secreting pituitary adenoma

SOCS2 polymorphisms are not associated with clinical and biochemical phenotypes in acromegalic patients

New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

Influence of growth hormone receptor (GHR) exon 3 and -202A/C IGFBP-3 genetic polymorphisms on clinical and biochemical features and therapeutic outcome of patients with acromegaly

The Interactive Effect of GHR-Exon 3 and −202 A/C IGFBP3 Polymorphisms on rhGH Responsiveness and Treatment Outcomes in Patients with Turner Syndrome

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

Evaluation of Downstream Regulatory Element Antagonistic Modulator Gene in Human Multinodular Goiter

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren

Copy number variation associated with Kallmann syndrome： new genetics insights from genome-wide studies

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