scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1053147731 |
P356 | DOI | 10.1186/1755-8166-2-19 |
P932 | PMC publication ID | 2761935 |
P698 | PubMed publication ID | 19781104 |
P5875 | ResearchGate publication ID | 26837971 |
P50 | author | Simona Baronchelli | Q57058515 |
Nicoletta Villa | Q92145326 | ||
Leda Dalprà | Q114563955 | ||
P2093 | author name string | Valeria Lucchini | |
Pietro Cavalli | |||
Sara Lissoni | |||
Enrico Betri | |||
P2860 | cites work | Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes | Q21145278 |
Cell cycle-dependent translocation of PRC1 on the spindle by Kif4 is essential for midzone formation and cytokinesis | Q24557528 | ||
Mutations in SRY and SOX9: testis-determining genes | Q28237671 | ||
Movement of the X chromosome in epilepsy | Q28292834 | ||
Genome architecture, rearrangements and genomic disorders | Q29614721 | ||
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: experiment | Q33268717 | ||
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 nucleus | Q34831329 | ||
X inactivation and the complexities of silencing a sex chromosome | Q34983583 | ||
A stain upon the silence: genes escaping X inactivation | Q35193727 | ||
Spatial genome organization in the formation of chromosomal translocations | Q35650635 | ||
The genome and the nucleus: a marriage made by evolution. Genome organisation and nuclear architecture | Q36245342 | ||
Spatial organization of active and inactive genes and noncoding DNA within chromosome territories | Q36325226 | ||
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 function | Q36955679 | ||
The Barr body is a looped X chromosome formed by telomere association | Q37548641 | ||
Inverted repeat structure of the human genome: the X-chromosome contains a preponderance of large, highly homologous inverted repeats that contain testes genes | Q37593039 | ||
Alteration of nuclear architecture in male germ cells of chromosomally derived subfertile mice | Q38490800 | ||
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Preservation of large-scale chromatin structure in FISH experiments. | Q40205728 | ||
Familial X/Y translocations associated with variable sexual phenotype | Q43011466 | ||
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 chromosome | Q50935888 | ||
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 | ||
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Position effect in human genetic disease | Q59662080 | ||
X;Y translocation in a female with streak gonads, H-Y- phenotype, and some features of Turner's syndrome | Q70585171 | ||
X-Y translocation. A case report | Q70646325 | ||
Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea | Q73549626 | ||
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes | Q74521256 | ||
Histologic analysis of gonadal tissue in patients with Ullrich-Turner syndrome and derivative Y chromosomes | Q81476841 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P921 | main subject | premature ovarian failure | Q647630 |
P304 | page(s) | 19 | |
P577 | publication date | 2009-09-27 | |
P1433 | published in | Molecular Cytogenetics | Q15761790 |
P1476 | title | Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship? | |
P478 | volume | 2 |
Q33795733 | A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning. |
Q37362935 | A de novo Reciprocal X; 9 Translocation in A Patient with Premature Ovarian Failure |
Q48571276 | Are FSHR polymorphisms risk factors to premature ovarian insufficiency? |
Q37721316 | Balanced Reciprocal Translocation t(X;1) in a Girl with Tall Stature and Primary Amenorrhea |
Q34521311 | Cytogenetics of premature ovarian failure: an investigation on 269 affected women. |
Q36237122 | Investigating the role of X chromosome breakpoints in premature ovarian failure. |
Q54212672 | Next generation sequencing identifies abnormal Y chromosome and candidate causal variants in premature ovarian failure patients. |
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