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Nicolas Jullien

Aix-Marseille University

17

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166

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Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination

2020 Methods
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Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells.

2020 Molecular Psychiatry
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MT5-MMP controls APP metabolism and the fate of beta-CTF/C99 and Abeta through proteolytic-dependent and -independent mechanisms relevant for Alzheimer's disease

2020 bioRxiv
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Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.

2020 Clinical Endocrinology
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Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

2019 European Journal of Human Genetics
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MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency

2016 European Journal of Endocrinology
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GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency.

2016 Hormone and Metabolic Research
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Réseau GENHYPOPIT : analyse phénotype/génotype des hypopituitarismes congénitaux (1213 patients)

2016 Archives De Pediatrie
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LHX3 et déficit hypophysaire congénital : 1re mutation identifiée à l’état homozygote

2015 Annales D Endocrinologie
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Combined pituitary hormone deficiency: current and future status

2015 Journal of Endocrinological Investigation
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Citations (26)