ライフサイエンスコーパス: X-chromosome gene

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1 and XX cells may have a higher dose of some X-chromosome genes.

2 ons in the fly for 2-fold activation of male X-chromosome genes.

3 to synonymous substitution rates (dN/dS) on X-chromosome genes.

4 lasia congenita (AHC) critical region on the X chromosome, gene 1] is an orphan nuclear receptor that

5 In mammals, X chromosome genes are present in one copy in males and

6 omparative genomics, we find that these same X-chromosome genes are exceptionally poorly conserved in

7 This demonstration of an X chromosome gene as a disease susceptibility factor in

8 n exon 1 of the human androgen receptor (AR) X chromosome gene assay (HUMARA) has been used to determ

9 Six of 783 non-pseudoautosomal region (PAR) X-chromosome genes (ATRX, CNKSR2, DDX3X, KDM5C, KDM6A, a

10 or detecting the transcripts of 2 additional X-chromosome genes: Bruton tyrosine kinase (BTK) and 4-a

11 further deletions and duplications affecting X chromosome genes but without apparent disease conseque

12 A subset of X-chromosome genes can escape X-inactivation, which woul

13 of existing genes contribute to the unusual X chromosome gene content.

14 on of Y-chromosomes across fly species.While X-chromosome gene content tends to be conserved, Y-chrom

15 the-first) is required for the regulation of X chromosome gene dosage compensation in Drosophila male

16 X-chromosome gene dosage is compensated by a specialized

17 SLE susceptibility is partly explained by an X chromosome gene-dose effect.

18 Dosage compensation, the equalized X chromosome gene expression between males and females i

19 s in early embryonic development, equalizing X chromosome gene expression between males and females.

20 higher order chromosome structure and proper X chromosome gene expression.

21 f the C. elegans mitotic machinery regulates X chromosome gene expression.

22 occurring human model for the study of both X-chromosome gene expression and androgen on brain devel

23 ial process of dosage compensation equalizes X-chromosome gene expression between Caenorhabditis eleg

24 We also show that the DCC balances X-chromosome gene expression between sexes by controllin

25 , and mammals, dosage compensation equalizes X-chromosome gene expression between the sexes through c

26 ers new insight into the relationships among X-chromosome gene expression, neuroanatomy, and cognitiv

27 young male with a hemizygous mutation in the X-chromosome gene FIGF (c.352 G>A) associated with early

28 We sequenced introns from 22 X chromosome genes in M and S from two locations of West

29 ation that loss of function of 1% or more of X-chromosome genes is compatible with apparently normal

30 E-1 transposons are strongly enriched on the X chromosome, genes located on the X chromosome are also

31 d on the cell surface because of an acquired X-chromosome gene mutation.

32 ome phenotype and, thus, demonstrate that an X chromosome gene (or genes) regulates HSC replication,

33 on detection of exonic polymorphisms of the X chromosome genes p55 and G6PD using rtPCR-LDR.

34 that males and females have equal amounts of X-chromosome gene products.

35 ed on quantitative expression of polymorphic X chromosome genes (qTCA) and found no evidence of clona

36 Chromosome segregation and X-chromosome gene regulation in Caenorhabditis elegans s

37 The X-chromosome gene regulatory process called dosage compe

38 and report a dramatic underrepresentation of X-chromosome genes showing high relative expression in m

39 m cell elimination associated with defective X chromosome gene silencing and sex chromosome condensat

40 This suggests an alternative X-chromosome gene, that escapes inactivation, is respons

41 blood cell disorder due to mutations of the X-chromosome gene WASP (Wiskott-Aldrich syndrome protein

42 ch syndrome (WAS) arises from defects of the X-chromosome gene WASP.

43 We show that X chromosome genes with male-biased expression are under

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