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Justine Bouilly

Showing results (11-20 of 19) with videos related to

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Human Molecular Genetics|November 1, 2016
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiencyIlaria Ferrari, Justine Bouilly, Isabelle Beau, et al.
The Journal of Clinical Investigation|September 26, 2012
Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administrationCharlotte Sonigo, Justine Bouilly, Nadège Carré, et al.
Annals of Hematology|November 30, 2018
Primary hepatic marginal B cell lymphoma of mucosa-associated lymphoid tissue (MALT) and non-alcoholic steatohepatitis (NASH): more than a coincidence?Simon Haefliger, Dina Milowich, Amedeo Sciarra, et al.
Cancers|December 2, 2020
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in Asia Frequently Shows <i>SETD2</i> AlterationsSakura Tomita, Yara Yukie Kikuti, Joaquim Carreras, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian InsufficiencyJustine Bouilly, Isabelle Beau, Sara Barraud, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2014
New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expressionJustine Bouilly, Florence Roucher-Boulez, Anne Gompel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 18, 2022
Nodal cytotoxic peripheral T-cell lymphoma occurs frequently in the clinical setting of immunodysregulation and is associated with recurrent epigenetic alterationsAlina Nicolae, Justine Bouilly, Diane Lara, et al.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Molecular Genetics|November 1, 2016
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiencyIlaria Ferrari, Justine Bouilly, Isabelle Beau, et al.
The Journal of Clinical Investigation|September 26, 2012
Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administrationCharlotte Sonigo, Justine Bouilly, Nadège Carré, et al.
Annals of Hematology|November 30, 2018
Primary hepatic marginal B cell lymphoma of mucosa-associated lymphoid tissue (MALT) and non-alcoholic steatohepatitis (NASH): more than a coincidence?Simon Haefliger, Dina Milowich, Amedeo Sciarra, et al.
Cancers|December 2, 2020
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in Asia Frequently Shows <i>SETD2</i> AlterationsSakura Tomita, Yara Yukie Kikuti, Joaquim Carreras, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian InsufficiencyJustine Bouilly, Isabelle Beau, Sara Barraud, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2014
New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expressionJustine Bouilly, Florence Roucher-Boulez, Anne Gompel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 18, 2022
Nodal cytotoxic peripheral T-cell lymphoma occurs frequently in the clinical setting of immunodysregulation and is associated with recurrent epigenetic alterationsAlina Nicolae, Justine Bouilly, Diane Lara, et al.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
Pageof 2