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  2. Barr body - Wikipedia

    en.wikipedia.org/wiki/Barr_body

    Barr bodies can be seen in neutrophils at the rim of the nucleus. In humans with more than one X chromosome, the number of Barr bodies visible at interphase is always one fewer than the total number of X chromosomes. For example, people with Klinefelter syndrome (47, XXY) have a single Barr body, and people with a 47, XXX karyotype have two ...

  3. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    In the past, the observation of the Barr body was common practice, as well. [47] To investigate the presence of a possible mosaicism, analysis of the karyotype using cells from the oral mucosa is performed. Physical characteristics of a Klinefelter syndrome can be tall stature, low body hair, and occasionally an enlargement of the breast.

  4. Ataxia–telangiectasia - Wikipedia

    en.wikipedia.org/wiki/Ataxia–telangiectasia

    ATM is located on human chromosome 11 (11q22.3) and is made up of 69 exons spread across 150kb of genomic DNA. [25] The mode of inheritance for A–T is autosomal recessive. Each parent is a carrier, meaning that they have one normal copy of the A–T gene (ATM) and one copy that is mutated.

  5. X-inactivation - Wikipedia

    en.wikipedia.org/wiki/X-inactivation

    The Xist gene is expressed at high levels on the Xi and is not expressed on the Xa. [39] Many other genes escape inactivation; some are expressed equally from the Xa and Xi, and others, while expressed from both chromosomes, are still predominantly expressed from the Xa. [40] [41] [42] Up to one quarter of genes on the human Xi are capable of ...

  6. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    Humans have FN = 82, [35] due to the presence of five acrocentric chromosome pairs: 13, 14, 15, 21, and 22 (the human Y chromosome is also acrocentric). The fundamental autosomal number or autosomal fundamental number, FNa [ 36 ] or AN , [ 37 ] of a karyotype is the number of visible major chromosomal arms per set of autosomes (non- sex-linked ...

  7. Sex-chromosome dosage compensation - Wikipedia

    en.wikipedia.org/wiki/Sex-chromosome_dosage...

    Additionally, 10-25% of human X chromosome genes, [12] and 3-7% of mouse X chromosome genes [13] outside of the PARs show weak expression from the inactive X chromosome. Random X-inactivation demands that the cell can determine if it contains more than one active X-chromosome before acting to silence any extraneous X-chromosome(s).

  8. Genetic profile may predict best response to weight-loss drug ...

    www.aol.com/news/genetic-profile-may-predict...

    Certain genes may identify patients with obesity who are most likely to respond strongly to Novo Nordisk's weight-loss drug Wegovy, researchers reported on Monday. The study, released at the ...

  9. X-linked lymphoproliferative disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_lymphoproliferat...

    X-linked lymphoproliferative disease; Other names: Duncan disease, Purtilo syndrome: Specialty: Hematology : Symptoms: Reduced resistance to the Epstein-Barr virus (EBV), leading to infectious mononucleosis, hemophagocytic lymphohistiocytosis (HLH), dysgammaglobulinemia, non-Hodgkin lymphoma, aplastic anemia, vasculitis, chronic gastritis, skin lesions