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The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling

Genes & development, 2012-10, Vol.26 (20), p.2299-2310

2012

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Emerging trends in the diagnosis and treatment of acromegaly in Canada

Clinical endocrinology (Oxford), 2013-07, Vol.79 (1), p.79-85

2013

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Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease

Genes & development, 2006-10, Vol.20 (20), p.2871-2886

2006

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Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3329-3336

2006

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Tpit determines alternate fates during pituitary cell differentiation

Genes & development, 2003-03, Vol.17 (6), p.738-747

2003

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Cooperation between Cyclin E and p27Kip1 in Pituitary Tumorigenesis

Molecular endocrinology (Baltimore, Md.), 2010-09, Vol.24 (9), p.1835-1845

2010

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Oral estroprogestin: an alternative low cost therapy for women with postoperative persistent acromegaly

Pituitary, 2010-12, Vol.13 (4), p.311-314

2010

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Cooperation between cyclin E and p27(Kip1) in pituitary tumorigenesis

Molecular endocrinology (Baltimore, Md.), 2010-09, Vol.24 (9), p.1835-1845

2010

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Differential Regulation of Proopiomelanocortin and Pituitary-Restricted Transcription Factor (TPIT), a New Marker of Normal and Adenomatous Human Corticotrophs

The journal of clinical endocrinology and metabolism, 2003-07, Vol.88 (7), p.3050-3056

2003

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Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations

Hormone research in paediatrics, 2016-01, Vol.85 (4), p.283-287

2016

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Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations

The journal of clinical endocrinology and metabolism, 2012-03, Vol.97 (3), p.E486-E495

2012

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Long-term cabergoline therapy is not associated with valvular heart disease in patients with prolactinomas

Pituitary, 2009, Vol.12 (3), p.153-157

2009

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Pasireotide monotherapy in Cushing’s disease: a single-centre experience with 5-year extension of phase III Trial

Pituitary, 2014-12, Vol.17 (6), p.519-529

2014

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Cabergoline therapy for prolactinomas: is valvular heart disease a real safety concern?

Expert review of cardiovascular therapy, 2010-01, Vol.8 (1), p.49-54

2010

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Octreotide LAR for the treatment of acromegaly

Expert opinion on drug metabolism & toxicology, 2008-06, Vol.4 (6), p.783-793

2008

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Macroprolactinemia Revisited: A Study on 106 Patients

The journal of clinical endocrinology and metabolism, 2002-02, Vol.87 (2), p.581-588

2002

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Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Genes & development, 2003-03, Vol.17 (6), p.711-716

2003

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Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations

The journal of clinical endocrinology and metabolism, 2005-03, Vol.90 (3), p.1323-1331

2005

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The TPIT Gene Mutation M86R Associated with Isolated Adrenocorticotropin Deficiency Interferes with Protein: Protein Interactions

The journal of clinical endocrinology and metabolism, 2007-10, Vol.92 (10), p.3991-3999

2007

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Tpit- -NeuroD1- - Mice Reveal Novel Aspects of Corticotroph Development

Endocrine research, 2004-01, Vol.30 (4), p.551-552

2004

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An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain

The journal of clinical endocrinology and metabolism, 2005-08, Vol.90 (8), p.4880-4887

2005

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The desmopressin test as a predictive factor of outcome after pituitary surgery for Cushing's disease

European journal of endocrinology, 2004-12, Vol.151 (6), p.727

2004

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A Familial Form of Congenital Hypopituitarism Due to a PROP1 Mutation in a Large Kindred: Phenotypic and in Vitro Functional Studies

The journal of clinical endocrinology and metabolism, 2004-11, Vol.89 (11), p.5779-5786

2004

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Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene

Pediatrics (Evanston), 2006-02, Vol.117 (2), p.e322

2006

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Identification and Functional Analysis of the Novel S179R POU1F1 Mutation Associated with Combined Pituitary Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2006-12, Vol.91 (12), p.4981-4987

2006

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The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling

Emerging trends in the diagnosis and treatment of acromegaly in Canada

Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease

Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients

Tpit determines alternate fates during pituitary cell differentiation

Cooperation between Cyclin E and p27Kip1 in Pituitary Tumorigenesis

Oral estroprogestin: an alternative low cost therapy for women with postoperative persistent acromegaly

Cooperation between cyclin E and p27(Kip1) in pituitary tumorigenesis

Differential Regulation of Proopiomelanocortin and Pituitary-Restricted Transcription Factor (TPIT), a New Marker of Normal and Adenomatous Human Corticotrophs

Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations

Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations

Long-term cabergoline therapy is not associated with valvular heart disease in patients with prolactinomas

Pasireotide monotherapy in Cushing’s disease: a single-centre experience with 5-year extension of phase III Trial

Cabergoline therapy for prolactinomas: is valvular heart disease a real safety concern?

Octreotide LAR for the treatment of acromegaly

Macroprolactinemia Revisited: A Study on 106 Patients

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations

The TPIT Gene Mutation M86R Associated with Isolated Adrenocorticotropin Deficiency Interferes with Protein: Protein Interactions

Tpit- -NeuroD1- - Mice Reveal Novel Aspects of Corticotroph Development

An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain

The desmopressin test as a predictive factor of outcome after pituitary surgery for Cushing's disease

A Familial Form of Congenital Hypopituitarism Due to a PROP1 Mutation in a Large Kindred: Phenotypic and in Vitro Functional Studies

Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene

Identification and Functional Analysis of the Novel S179R POU1F1 Mutation Associated with Combined Pituitary Hormone Deficiency

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