Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?

scientific article published on 27 September 2009

Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship? is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1053147731
P356DOI10.1186/1755-8166-2-19
P932PMC publication ID2761935
P698PubMed publication ID19781104
P5875ResearchGate publication ID26837971

P50authorSimona BaronchelliQ57058515
Nicoletta VillaQ92145326
Leda DalpràQ114563955
P2093author name stringValeria Lucchini
Pietro Cavalli
Sara Lissoni
Enrico Betri
P2860cites workGenomic disorders: molecular mechanisms for rearrangements and conveyed phenotypesQ21145278
Cell cycle-dependent translocation of PRC1 on the spindle by Kif4 is essential for midzone formation and cytokinesisQ24557528
Mutations in SRY and SOX9: testis-determining genesQ28237671
Movement of the X chromosome in epilepsyQ28292834
Genome architecture, rearrangements and genomic disordersQ29614721
Rise, fall and resurrection of chromosome territories: a historical perspective. Part II. Fall and resurrection of chromosome territories during the 1950s to 1980s. Part III. Chromosome territories and the functional nuclear architecture: experimentQ33268717
The molecular action and regulation of the testis-determining factors, SRY (sex-determining region on the Y chromosome) and SOX9 [SRY-related high-mobility group (HMG) box 9].Q33338634
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.Q33412558
Differences in the localization and morphology of chromosomes in the human nucleus.Q33864702
Chromosome territories--a functional nuclear landscape.Q34523990
Chromosome positioning in the interphase nucleusQ34831329
X inactivation and the complexities of silencing a sex chromosomeQ34983583
A stain upon the silence: genes escaping X inactivationQ35193727
Spatial genome organization in the formation of chromosomal translocationsQ35650635
The genome and the nucleus: a marriage made by evolution. Genome organisation and nuclear architectureQ36245342
Spatial organization of active and inactive genes and noncoding DNA within chromosome territoriesQ36325226
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature.Q36404667
Random X-chromosome inactivation: skewing lessons for mice and men.Q36463848
Three-dimensional genome organization in interphase and its relation to genome functionQ36955679
The Barr body is a looped X chromosome formed by telomere associationQ37548641
Inverted repeat structure of the human genome: the X-chromosome contains a preponderance of large, highly homologous inverted repeats that contain testes genesQ37593039
Alteration of nuclear architecture in male germ cells of chromosomally derived subfertile miceQ38490800
Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocationQ38491467
Preservation of large-scale chromatin structure in FISH experiments.Q40205728
Familial X/Y translocations associated with variable sexual phenotypeQ43011466
Variability of sexual phenotype in 46,XX(SRY+) patients: the influence of spreading X inactivation versus position effects.Q43073259
Mapping the locus of the H-Y gene on the human Y chromosomeQ50935888
Nuclear reorganisation and chromatin decondensation are conserved, but distinct, mechanisms linked to Hox gene activation.Q51996175
Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.Q52091534
Cell biology: chromosome territories.Q55042988
Position effect in human genetic diseaseQ59662080
X;Y translocation in a female with streak gonads, H-Y- phenotype, and some features of Turner's syndromeQ70585171
X-Y translocation. A case reportQ70646325
Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoeaQ73549626
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genesQ74521256
Histologic analysis of gonadal tissue in patients with Ullrich-Turner syndrome and derivative Y chromosomesQ81476841
P4510describes a project that usesImageJQ1659584
P921main subjectpremature ovarian failureQ647630
P304page(s)19
P577publication date2009-09-27
P1433published inMolecular CytogeneticsQ15761790
P1476titleChromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?
P478volume2

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cites work (P2860)
Q33795733A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning.
Q37362935A de novo Reciprocal X; 9 Translocation in A Patient with Premature Ovarian Failure
Q48571276Are FSHR polymorphisms risk factors to premature ovarian insufficiency?
Q37721316Balanced Reciprocal Translocation t(X;1) in a Girl with Tall Stature and Primary Amenorrhea
Q34521311Cytogenetics of premature ovarian failure: an investigation on 269 affected women.
Q36237122Investigating the role of X chromosome breakpoints in premature ovarian failure.
Q54212672Next generation sequencing identifies abnormal Y chromosome and candidate causal variants in premature ovarian failure patients.

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