Impaired protein stability and nuclear localization ofNOBOXvariants associated with premature ovarian insufficiency

NOBOXis a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency

(2016) N. Bouali et al.   CLINICAL GENETICS

ESHRE Guideline: management of women with premature ovarian insufficiency

(2016)   HUMAN REPRODUCTION

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency

(2016) Justine Bouilly et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Physiological and pathophysiological role of nonsense-mediated mRNA decay

(2016) Franziska Ottens et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

The Biology of Proteostasis in Aging and Disease

(2015) Johnathan Labbadia et al.   Annual Review of Biochemistry

Genetics of primary ovarian insufficiency: new developments and opportunities

(2015) Yingying Qin et al.   HUMAN REPRODUCTION UPDATE

NewNOBOXMutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency DecreaseKIT-LExpression

(2015) Justine Bouilly et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis

(2015) Ariella Weinberg-Shukron et al.   JOURNAL OF CLINICAL INVESTIGATION

Pharmacologic agents targeting autophagy

(2015) Helin Vakifahmetoglu-Norberg et al.   JOURNAL OF CLINICAL INVESTIGATION

Genetics of the ovarian reserve

(2015) Emanuele Pelosi et al.   Frontiers in Genetics

GDF9 is Transiently Expressed in Oocytes before Follicle Formation in the Human Fetal Ovary and is Regulated by a Novel NOBOX Transcript

(2015) Rosemary A. L. Bayne et al.   PLoS One

NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis

(2014) Justine Bouilly et al.   Journal of Molecular Cell Biology

Biomarkers of Ovarian Reserve—Do They Predict Somatic Aging?

(2013) Marcelle Cedars   SEMINARS IN REPRODUCTIVE MEDICINE

FOXL2 Impairment in Human Disease

(2012) Hannah Verdin et al.   Hormone Research in Paediatrics

Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort

(2011) Justine Bouilly et al.   HUMAN MUTATION

Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown

(2011) Agnieszka Lechowska et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Oogenesis: Transcriptional regulators and mouse models

(2011) Krishna Jagarlamudi et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

SUMOylation of the Forkhead Transcription Factor FOXL2 Promotes Its Stabilization/Activation through Transient Recruitment to PML Bodies

(2011) Adrien Georges et al.   PLoS One

Genes involved in human premature ovarian failure

(2010) Luca Persani et al.   JOURNAL OF MOLECULAR ENDOCRINOLOGY

Premature ovarian failure

(2010) Andrew N Shelling   REPRODUCTION

Is there a trade-off between fertility and longevity? A comparative study of women from three large historical databases accounting for mortality selection

(2009) Alain Gagnon et al.   AMERICAN JOURNAL OF HUMAN BIOLOGY

BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein

(2009) Raffaella Rossetti et al.   HUMAN MUTATION

UMD-predictor, a new prediction tool for nucleotide substitution pathogenicity-application to four genes:FBN1,FBN2,TGFBR1, andTGFBR2

(2009) Mélissa Yana Frédéric et al.   HUMAN MUTATION

The role of the nuclear transport system in cell differentiation

(2009) Noriko Yasuhara et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Mutation analysis of NOBOX homeodomain in chinese women with premature ovarian failure

(2008) Yingying Qin et al.   FERTILITY AND STERILITY

Protein interactions in human genetic diseases

(2008) Benjamin Schuster-Böckler et al.   GENOME BIOLOGY