Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.
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Genetics of primary ovarian insufficiency: new developments and opportunitiesEnvironmentally induced epigenetic transgenerational inheritance of ovarian diseaseControl of Oocyte Reawakening by Kit.The genetics of premature ovarian failure: current perspectivesA non-sense MCM9 mutation in a familial case of primary ovarian insufficiencyGenomic markers of ovarian reserveTransplantation of human menstrual blood stem cells to treat premature ovarian failure in mouse model.Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders.Genetics of primary ovarian insufficiency: a reviewDeleterious mutation in SYCE1 is associated with non-obstructive azoospermia.A chromosome 19 locus positively influences the number of retrieved oocytes during stimulated cycles in Brazilian womenInvestigating the role of X chromosome breakpoints in premature ovarian failure.CD44+/CD105+ human amniotic fluid mesenchymal stem cells survive and proliferate in the ovary long-term in a mouse model of chemotherapy-induced premature ovarian failureMulti-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation.Growth hormone treatment of premature ovarian failure in a mouse model via stimulation of the Notch-1 signaling pathway.Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure casesArray-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology.Induction of estrogen-sensitive epithelial cells derived from human-induced pluripotent stem cells to repair ovarian function in a chemotherapy-induced mouse model of premature ovarian failureThe Genetics of Infertility: Current Status of the Field.Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome.Premature ovarian failure: a critical condition in the reproductive potential with various genetic causes.Gene copy number variation analysis reveals dosage-insensitive expression of CYP2E1.Genetics of primary ovarian insufficiency.Restoring Ovarian Function With Human Placenta-Derived Mesenchymal Stem Cells in Autoimmune-Induced Premature Ovarian Failure Mice Mediated by Treg Cells and Associated Cytokines.
P2860
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P2860
Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.
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2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genomic analysis using high-re ...... ith premature ovarian failure.
@ast
Genomic analysis using high-re ...... ith premature ovarian failure.
@en
Genomic analysis using high-re ...... ith premature ovarian failure.
@nl
type
label
Genomic analysis using high-re ...... ith premature ovarian failure.
@ast
Genomic analysis using high-re ...... ith premature ovarian failure.
@en
Genomic analysis using high-re ...... ith premature ovarian failure.
@nl
prefLabel
Genomic analysis using high-re ...... ith premature ovarian failure.
@ast
Genomic analysis using high-re ...... ith premature ovarian failure.
@en
Genomic analysis using high-re ...... ith premature ovarian failure.
@nl
P2093
P2860
P1476
Genomic analysis using high-re ...... ith premature ovarian failure.
@en
P2093
Aleksandar Rajkovic
Ertug Kovanci
Hyo Won Ahn
Megan M McGuire
Natalie J Engel
Wayne Bowden
P2860
P304
P356
10.1016/J.FERTNSTERT.2010.12.052
P407
P577
2011-01-22T00:00:00Z