Identification of novel mutations in FOXL2 associated with premature ovarian failure
about
Premature ovarian failureScreening for known mutations in EIF2Bgenes in a large panel of patients with premature ovarian failureOvarian failure related to eukaryotic initiation factor 2B mutations.FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlationContemporary genetic technologies and female reproductionGenetics of primary ovarian insufficiency: new developments and opportunitiesThe genetics of premature ovarian failure: current perspectivesMCM9 mutations are associated with ovarian failure, short stature, and chromosomal instabilitySUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodiesGenomic markers of ovarian reserveThe pathway to femaleness: current knowledge on embryonic development of the ovary.Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeGenome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.The transcriptional targets of mutant FOXL2 in granulosa cell tumours.Transcriptional regulation of early oogenesis: in search of masters.An investigation into FOXE1 polyalanine tract length in premature ovarian failure.The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2.Genetics of primary ovarian insufficiency: a reviewIdentifying a novel role for X-prolyl aminopeptidase (Xpnpep) 2 in CrVI-induced adverse effects on germ cell nest breakdown and follicle development in rats.Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndromeFOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failureInvestigating the role of X chromosome breakpoints in premature ovarian failure.The genetic basis of premature ovarian failure.Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndromeOrganogenesis of the ovary: a comparative review on vertebrate ovary formationFOXL2 molecular status in adult granulosa cell tumors of the ovary: A study of primary and metastatic casesMolecular analysis of FOXC1 in subjects presenting with severe developmental eye anomaliesThe Genetics of Infertility: Current Status of the Field.The potential role of microRNAs in regulating gonadal sex differentiation in the chicken embryo.Genetics of primary ovarian insufficiency.Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations.A genomic basis for the evolution of vertebrate transcription factors containing amino Acid runs.Premature Ovarian Insufficiency - an update on recent advances in understanding and management.Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions.Ablation of beta subunit of protein kinase CK2 in mouse oocytes causes follicle atresia and premature ovarian failure.
P2860
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P2860
Identification of novel mutations in FOXL2 associated with premature ovarian failure
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
name
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@ast
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en-gb
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@nl
type
label
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@ast
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en-gb
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@nl
prefLabel
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@ast
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en-gb
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@nl
P2093
P356
P1476
Identification of novel mutations in FOXL2 associated with premature ovarian failure
@en
P2093
A N Shelling
I M Winship
K Aittomäki
S E Harris
P304
P356
10.1093/MOLEHR/8.8.729
P407
P577
2002-08-01T00:00:00Z