I. Pellegrini-Bouiller

Author

Institut de Neurobiologie de la Méditerranée

Also Known As

I Pellegrini-Bouiller, I. Pellegrini-Bouiller, I.P. Pellegrini-Bouiller, Isabelle Pellegrini-Bouiller

Publications

588

Citations

H-Index

Concepts

All Affiliations

Institut de Neurobiologie de la Méditerranée Centre National de la Recherche Scientifique Roche (Switzerland)Centre National pour la Recherche Scientifique et Technique (CNRST)Roche (France)

About

I. Pellegrini-Bouiller is an author at Institut de Neurobiologie de la Méditerranée specializing in gene expression, medicine, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	206
2	Endocrinology	4	4	187
3	Cell Biology	3	3	71
4	Molecular Genetics	2	2	135
5	Immunology	1	1	21

I. Pellegrini-Bouiller

Publications

515

Citations

H-Index

Page 1

	Year	Citations
PROP1 Gene Screening in Patients with Multiple Pituitary Hormone Deficiency Reveals Two Sites of Hypermutability and a High Incidence of Corticotroph Deficiency Sophie Vallette-Kasic, Anne Barlier, Cécile Teinturier, The Journal of Clinical Endocrinology & Metabolism	2001	120
A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency. I. Pellegrini-Bouiller, P. Bélicar, Anne Barlier, The Journal of Clinical Endocrinology & Metabolism Human GrowthGeneticsPathologyTranscription Factor Pit-1Molecular Genetics	1996	93
Impact of<i>gsp</i>Oncogene on the Expression of Genes Coding for G<sub>s</sub>α, Pit-1, G<sub>i</sub>2α, and Somatostatin Receptor 2 in Human Somatotroph Adenomas: Involvement in Octreotide Sensitivity<sup>1</sup> Anne Barlier, I. Pellegrini-Bouiller, Ginette Gunz, The Journal of Clinical Endocrinology & Metabolism	1999	72
A Familial Form of Congenital Hypopituitarism Due to a<i>PROP1</i>Mutation in a Large Kindred: Phenotypic and<i>in Vitro</i>Functional Studies Rachel Reynaud, M. Chadli-Chaieb, Sophie Vallette-Kasic, The Journal of Clinical Endocrinology & Metabolism	2004	71
Expression of the Members of the Ptx Family of Transcription Factors in Human Pituitary Adenomas<sup>1</sup> I. Pellegrini-Bouiller, Christine Manrique, Ginette Gunz, The Journal of Clinical Endocrinology & Metabolism	1999	46
A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency I. Pellegrini-Bouiller The Journal of Clinical Endocrinology & Metabolism New MutationTranscriptional RegulationDevelopmental BiologyPituitary GlandGrowth Hormone	1996	42
Combined Pituitary Hormone Deficiency due to the F135C Human Pit-1 (Pituitary-Specific Factor 1) Gene Mutation: Functional and Structural Correlates Sophie Vallette-Kasic, I. Pellegrini-Bouiller, Franĉois Sampiéri, Molecular Endocrinology Transcriptional RegulationDevelopmental BiologyPituitary GlandGrowth HormoneGenetics	2001	31
Pit-1 gene expression in human lactotroph and somatotroph pituitary adenomas is correlated to D2 receptor gene expression. I. Pellegrini-Bouiller, I Morange-Ramos, Anne Barlier, The Journal of Clinical Endocrinology & Metabolism D2 Receptor GeneHuman GrowthImmunologyPathologyMammary Gland Development	1996	21
Expression of the Members of the Ptx Family of Transcription Factors in Human Pituitary Adenomas I. Pellegrini-Bouiller The Journal of Clinical Endocrinology & Metabolism Systems BiologySignal TransductionPituitary GlandHuman Pituitary AdenomasPituitary Disease	1999	19

Page 1