Results 311 to 320 of about 6,305,601 (337)
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Mammalian Genome, 1997
Overall, the probe map fromDXWas70 toAmg encompasses 72 cM and includes 103 loci. Eight of these have been designated reference loci (see Table 2 and previous section) on account of their wide usage that would enable the cross reference of independent maps created in different laboratories.
Christine M. Disteche +6 more
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Overall, the probe map fromDXWas70 toAmg encompasses 72 cM and includes 103 loci. Eight of these have been designated reference loci (see Table 2 and previous section) on account of their wide usage that would enable the cross reference of independent maps created in different laboratories.
Christine M. Disteche +6 more
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Chromosome 9 of Ellobius lutescens is the X chromosome [PDF]
Chromosoma, 1988 Ellobius lutescens carries an apparently identical karyotype (2n = 17) in both sexes. On the basis of indirect evidence the unpaired chromosome 9 has been considered to represent the X chromosome of this species. We have obtained data to substantiate this view by four different techniques. After fusion of HPRT- RAG cells with E.
Sher Ali +5 more
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Methylation and the X chromosome
BioEssays, 1986AbstractRecent approaches towards an understanding of the molecular basis of X‐chromosome inactivation in mammals suggest that regulation is due to multiple events including DNA methylation.
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Psychiatric Genetics, 1998
Researchers presented results of ongoing research to the X-chromosome workshop of the Fifth World Congress on Psychiatric Genetics, covering a wide range of disorders: X-linked infantile spasms; a complex phenotype associated with deletions of Xp11; male homosexuality; degree of handedness; bipolar affective disorder; schizophrenia; childhood onset ...
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Researchers presented results of ongoing research to the X-chromosome workshop of the Fifth World Congress on Psychiatric Genetics, covering a wide range of disorders: X-linked infantile spasms; a complex phenotype associated with deletions of Xp11; male homosexuality; degree of handedness; bipolar affective disorder; schizophrenia; childhood onset ...
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X Chromosome and Ovarian Failure
Seminars in Reproductive Medicine, 2007Genes for reproduction are enriched on the sex chromosomes and they may be involved in the many forms of X- or Y-linked infertility. Here we review the X-linked disorders of ovulation and we show that despite the relatively frequent observation of X chromosome rearrangements in women with ovarian dysgenesis or ovarian failure, the search for X-linked ...
Toniolo, Daniela, RIZZOLIO, Flavio
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Gene regulation in time and space during X-chromosome inactivation
Nature reviews. Molecular cell biology, 2022Agnese Loda, Samuel Collombet, E. Heard
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Canadian Journal of Genetics and Cytology, 1965
Our introduction to X-cliromosonie cartography came when a blood group disclosed itself to be X-linked and to have a frequency that made it, theoretically at any rate, almost the best imaginable niarlcer of the X (h~lann, Calian, Gelb, Fisher, Hamper, Tippett, Sanger and Race, 1962).
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Our introduction to X-cliromosonie cartography came when a blood group disclosed itself to be X-linked and to have a frequency that made it, theoretically at any rate, almost the best imaginable niarlcer of the X (h~lann, Calian, Gelb, Fisher, Hamper, Tippett, Sanger and Race, 1962).
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The X chromosome and systemic sclerosis
Current Opinion in Rheumatology, 2006Similar to the majority of autoimmune rheumatic diseases, systemic sclerosis is characterized by a striking female predominance superimposed on a predisposing genetic background. At least two genetic mechanisms have been proposed that play a role in susceptibility to systemic sclerosis; firstly the maintenance of immune tolerance via genes on the X ...
C. Selmi, P. Invernizzi, M. E. Gershwin
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MECHANISMS OF X-CHROMOSOME REGULATION
Annual Review of Genetics, 1988Article de synthese sur les mecanismes de l'inactivation des chromosomes X chez les mammiferes, stabilite de l'inactivation dans les lignees somatiques et phenomenes de ...
Grant, Stephen G, Chapman, Verne M
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Tetrasomy and pentasomy of the X chromosome
European Journal of Pediatrics, 2011We describe a newborn girl with a life-threatening laryngomalacia and extreme hypotonia. Genetic analysis revealed the very rare genetic condition mosaicism of 48,XXXX and 49,XXXXX (50/50). We here state that the degree of early hypotonia constitutes an important early prognostic feature in this syndrome.
Schoubben, Edith +5 more
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