First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
about
Human aneuploidy: mechanisms and new insights into an age-old problemRecombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant miceLoss of Centromere Cohesion in Aneuploid Human Oocytes Correlates with Decreased Kinetochore Localization of the Sac Proteins Bub1 and Bubr1New insights into human nondisjunction of chromosome 21 in oocytes.Arrested human embryos are more likely to have abnormal chromosomes than developing embryos from women of advanced maternal age.The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.The effects of female age on fecundity and pregnancy outcome.Fertility and maternal age strategies to improve pregnancy outcome.First-meiotic-division nondisjunction in human oocytes.Association between nondisjunction and maternal age in meiosis-II human oocytesChromosomal drive and the evolution of meiotic nondisjunction and trisomy in humans.Spontaneous abortions are reduced after preconception diagnosis of translocationsChromosome 21 detection in human oocyte fluorescence in situ hybridization: possible effect of maternal ageA study of meiotic segregation in a fertile human population following ovarian stimulation with recombinant FSH-LH.Chromosome abnormalities in the human oocyte.Meiotic Recombination: The Essence of Heredity.Parental age-related aneuploidy in human germ cells and offspring: a story of past and present.Chromosomal differences in susceptibility to meiotic aneuploidy.Features associated with reproductive ageing in female rhesus monkeys.Deficiency of ovarian ornithine decarboxylase contributes to aging-related egg aneuploidy in mice.Analysis of nine chromosome probes in first polar bodies and metaphase II oocytes for the detection of aneuploidies.Viable rabbits derived from reconstructed oocytes by germinal vesicle transfer after intracytoplasmic sperm injection (ICSI).Origin of trisomy: no evidence to support the ovarian mosaicism theory.Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.
P2860
Q24631178-6FB9FF11-DDAF-4AEA-88CB-FDF7775EDA50Q24671536-DCCFF491-E44C-4B11-BE7B-E22FA1DA3298Q28506066-9A8BC393-0277-4031-BB97-1C6A2C7BF481Q30841621-886853CD-A8FB-46C4-888B-F6C56D1897D1Q33325904-BF882F02-240B-4D3D-9FFC-3EF4291FEE5BQ33784903-F6FE745E-37FE-48E3-A22F-E1E61179C3F1Q34007112-B0B7509A-3E4C-4B1A-A24C-720BB44D9B77Q34395332-97E73C28-5207-4907-B0B8-EF32E3F69018Q34397252-3CBC48EE-48E5-46EC-9657-E299CB762C5FQ35248934-4E76730D-DA8D-4D32-807D-398572542128Q35882916-9FE9E823-B024-407E-B6D9-2E2E9CF82204Q35916406-62E25828-2278-4912-A69A-E2F67487AE4DQ36267654-5342A361-22E3-4DB4-B090-6BEB8D62F2F9Q36268516-65A81135-71ED-4A3B-80A3-73520752CD74Q36648727-18B9C745-32C1-47CD-A948-6A8560BC6516Q37832909-8163E5B2-F735-421F-B0CB-F6846773FA0FQ38618828-93CD0E4F-DC53-4410-A8DD-DF421D8DADE4Q40956476-974FFD5D-D405-4705-8C46-A8603600DE14Q41202601-2EEC2C9B-B25A-40A5-82EE-EA7C04898104Q42521938-7103557E-2FC5-45D8-911D-30A652B8B9ACQ48638157-7875BD08-8307-4A05-9732-47107B764E08Q48830208-54B398B8-4325-46D1-A67C-380E81C12A93Q50720178-7998EBC9-1AD6-4EDD-966D-F34AC80C3042Q51341015-539DACC0-0A2C-4E3F-A94E-848DC2627C34Q53388910-67C1620D-96A1-46FB-9E80-CAF515F3B561
P2860
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh-hant
name
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@en
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@nl
type
label
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@en
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@nl
prefLabel
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@en
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@nl
P2093
P356
P1476
First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.
@en
P2093
P304
P356
10.1159/000133631
P577
1994-01-01T00:00:00Z