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A Molecular Switch for Photoperiod Responsiveness in Mammals

Current biology, 2010-12, Vol.20 (24), p.2193-2198

2010

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Identification of Melatonin-Regulated Genes in the Ovine Pituitary Pars Tuberalis, a Target Site for Seasonal Hormone Control

Endocrinology (Philadelphia), 2008-11, Vol.149 (11), p.5527-5539

2008

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Entrainment of disrupted circadian behavior through inhibition of casein kinase 1 (CK1) enzymes

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (34), p.15240-15245

2010

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Identification of Eya3 and TAC1 as Long-Day Signals in the Sheep Pituitary

Current biology, 2010-05, Vol.20 (9), p.829-835

2010

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Encoding and Decoding Photoperiod in the Mammalian Pars Tuberalis

Neuroendocrinology, 2011-01, Vol.94 (2), p.101-112

DUPRE, Sandrine M

2011

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Photoperiodic regulation of cellular retinoic acid-binding protein 1, GPR50 and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

Journal of endocrinology, 2006-12, Vol.191 (3), p.687-698

2006

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Altered metabolism in the melatonin-related receptor (GPR50) knockout mouse

American journal of physiology: endocrinology and metabolism, 2008-01, Vol.294 (1), p.E176-E182

2008

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Both Thyroid Hormone Receptor (TR)β1 and TRβ2 Isoforms Contribute to the Regulation of Hypothalamic Thyrotropin-Releasing Hormone

Endocrinology (Philadelphia), 2004-05, Vol.145 (5), p.2337-2345

2004

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Circannual Clocks: Annual Timers Unraveled in Sheep

Current biology, 2007-03, Vol.17 (6), p.R216-R217

2007

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Répression transcriptionnelle du gène TRH

M.S. Médecine sciences, 2005-10, Vol.21 (10), p.854-859

2005

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Feedback on Hypothalamic TRH Transcription Is Dependent on Thyroid Hormone Receptor N Terminus

Molecular endocrinology (Baltimore, Md.), 2002-07, Vol.16 (7), p.1652-1666

2002

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Feedback on hypothalamic TRH transcription is dependent on thyroid hormone receptor N terminus

Molecular endocrinology (Baltimore, Md.), 2002-07, Vol.16 (7), p.1652-1666

2002

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Photoperiodic regulation of cellular retinoic acid-binding protein 1, GPR50 and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

Journal of endocrinology, 2009-11, Vol.203 (2), p.311-311

2009

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The identification of a conserved Eya3 signal and prolactin-releasing factors in the long day response of a seasonal mammal

Current biology, 2010-04, Vol.20 (9), p.829-835

2010

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Nuclear Corepressor and Silencing Mediator of Retinoic and Thyroid Hormone Receptors Corepressor Expression Is Incompatible with T3-Dependent TRH Regulation

Endocrinology (Philadelphia), 2001-12, Vol.142 (12), p.5321-5331

2001

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Both thyroid hormone receptor (TR)beta 1 and TR beta 2 isoforms contribute to the regulation of hypothalamic thyrotropin-releasing hormone

Endocrinology (Philadelphia), 2004-05, Vol.145 (5), p.2337-2345

2004

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Photoperiodic regulation of cellular retinol binding protein, CRBP1 [corrected] and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

Journal of endocrinology, 2006-12, Vol.191 (3), p.687-698

2006

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Transcriptional repression of the TRH gene

M.S. Médecine sciences, 2005-10, Vol.21 (10), p.854-859

2005

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Altered metabolism in the melatonin-related receptor (GPR50) knockout mouse

American journal of physiology: endocrinology and metabolism, 2008, Vol.57 (1)

2008

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Nuclear Corepressor and Silencing Mediator of Retinoic and Thyroid Hormone Receptors Corepressor Expression Is Incompatible with T 3 -Dependent TRH Regulation

Endocrinology (Philadelphia), 2001-12, Vol.142 (12), p.5321-5331

2001

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A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity

Orphanet journal of rare diseases, 2016-06, Vol.11 (1), p.84-84, Article 84

2016

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Varia

Sociologie du travail (Paris), 2023-02, Vol.65 (1)

2023

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A Molecular Switch for Photoperiod Responsiveness in Mammals

Identification of Melatonin-Regulated Genes in the Ovine Pituitary Pars Tuberalis, a Target Site for Seasonal Hormone Control

Entrainment of disrupted circadian behavior through inhibition of casein kinase 1 (CK1) enzymes

Identification of Eya3 and TAC1 as Long-Day Signals in the Sheep Pituitary

Encoding and Decoding Photoperiod in the Mammalian Pars Tuberalis

Photoperiodic regulation of cellular retinoic acid-binding protein 1, GPR50 and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

Altered metabolism in the melatonin-related receptor (GPR50) knockout mouse

Both Thyroid Hormone Receptor (TR)β1 and TRβ2 Isoforms Contribute to the Regulation of Hypothalamic Thyrotropin-Releasing Hormone

Circannual Clocks: Annual Timers Unraveled in Sheep

Répression transcriptionnelle du gène TRH

Feedback on Hypothalamic TRH Transcription Is Dependent on Thyroid Hormone Receptor N Terminus

Feedback on hypothalamic TRH transcription is dependent on thyroid hormone receptor N terminus

Photoperiodic regulation of cellular retinoic acid-binding protein 1, GPR50 and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

The identification of a conserved Eya3 signal and prolactin-releasing factors in the long day response of a seasonal mammal

Nuclear Corepressor and Silencing Mediator of Retinoic and Thyroid Hormone Receptors Corepressor Expression Is Incompatible with T3-Dependent TRH Regulation

Both thyroid hormone receptor (TR)beta 1 and TR beta 2 isoforms contribute to the regulation of hypothalamic thyrotropin-releasing hormone

Photoperiodic regulation of cellular retinol binding protein, CRBP1 [corrected] and nestin in tanycytes of the third ventricle ependymal layer of the Siberian hamster

Transcriptional repression of the TRH gene

Altered metabolism in the melatonin-related receptor (GPR50) knockout mouse

Nuclear Corepressor and Silencing Mediator of Retinoic and Thyroid Hormone Receptors Corepressor Expression Is Incompatible with T 3 -Dependent TRH Regulation

A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity

Determination of four homogeneous subgroups of patients with antiphospholipid syndrome: a cluster analysis based on 509 cases

A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings

Varia

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