Literature DB >> 33925963

Dosage Compensation in Females with X-Linked Metabolic Disorders.

Patrycja Juchniewicz1, Ewa Piotrowska2, Anna Kloska1, Magdalena Podlacha2, Jagoda Mantej2, Grzegorz Węgrzyn2, Stefan Tukaj2, Joanna Jakóbkiewicz-Banecka1.   

Abstract

Through the use of new genomic and metabolomic technologies, our comprehension of the molecular and biochemical etiologies of genetic disorders is rapidly expanding, and so are insights into their varying phenotypes. Dosage compensation (lyonization) is an epigenetic mechanism that balances the expression of genes on heteromorphic sex chromosomes. Many studies in the literature have suggested a profound influence of this phenomenon on the manifestation of X-linked disorders in females. In this review, we summarize the clinical and genetic findings in female heterozygotic carriers of a pathogenic variant in one of ten selected X-linked genes whose defects result in metabolic disorders.

Entities:  

Keywords:  X chromosome inactivation; X-linked inheritance; XCI; inborn errors of metabolism; metabolic disorders

Year:  2021        PMID: 33925963     DOI: 10.3390/ijms22094514

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  177 in total

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Journal:  J Inherit Metab Dis       Date:  2016-04-22       Impact factor: 4.982

2.  Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes.

Authors:  M Kaplan; E Beutler; H J Vreman; C Hammerman; E Levy-Lahad; P Renbaum; D K Stevenson
Journal:  Pediatrics       Date:  1999-07       Impact factor: 7.124

3.  Glucose-6-phosphate dehydrogenase activity in bipolar disorder and schizophrenia: Relationship to mitochondrial impairment.

Authors:  Joseph S Puthumana; William T Regenold
Journal:  J Psychiatr Res       Date:  2019-03-05       Impact factor: 4.791

4.  Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Authors:  B R Migeon; H W Moser; A B Moser; J Axelman; D Sillence; R A Norum
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

5.  Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency.

Authors:  Angelo Minucci; Paola Concolino; Francesca Vendittelli; Bruno Giardina; Cecilia Zuppi; Ettore Capoluongo
Journal:  Clin Biochem       Date:  2007-11-28       Impact factor: 3.281

6.  A new variant in PHKA2 is associated with glycogen storage disease type IXa.

Authors:  Carmen Rodríguez-Jiménez; Fernando Santos-Simarro; Ángel Campos-Barros; Carmen Camarena; Dolores Lledín; Elena Vallespín; Ángela Del Pozo; Rocío Mena; Pablo Lapunzina; Sonia Rodríguez-Nóvoa
Journal:  Mol Genet Metab Rep       Date:  2017-01-12

7.  An analysis of trends and distribution of the burden of road traffic injuries in Uganda, 2011 to 2015: a retrospective study.

Authors:  Frederick Oporia; Angela Nakanwagi Kisakye; Rebecca Nuwematsiko; Abdulgafoor Mahmood Bachani; John Bosco Isunju; Abdullah Ali Halage; Zziwa Swaibu; Lynn Muhimbuura Atuyambe; Olive Kobusingye
Journal:  Pan Afr Med J       Date:  2018-09-02

8.  Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes.

Authors:  Weiyin Zhou; Shu-Hong Lin; Sairah M Khan; Meredith Yeager; Stephen J Chanock; Mitchell J Machiela
Journal:  Sci Rep       Date:  2021-01-13       Impact factor: 4.996

9.  Clinical, Biochemical, and Genetic Characterization of Glycogen Storage Type IX in a Child with Asymptomatic Hepatomegaly.

Authors:  Jung Ah Kim; Ja Hye Kim; Beom Hee Lee; Gu-Hwan Kim; Yoon S Shin; Han-Wook Yoo; Kyung Mo Kim
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2015-06-29

10.  Biological control agent Rhizobium (=Agrobacterium) vitis strain ARK-1 suppresses expression of the essential and non-essential vir genes of tumorigenic R. vitis.

Authors:  Akira Kawaguchi; Mizuho Nita; Tomoya Ishii; Megumi Watanabe; Yoshiteru Noutoshi
Journal:  BMC Res Notes       Date:  2019-01-03
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  1 in total

1.  Human iPSC-derived cerebral organoids model features of Leigh syndrome and reveal abnormal corticogenesis.

Authors:  Alejandra I Romero-Morales; Gabriella L Robertson; Anuj Rastogi; Megan L Rasmussen; Hoor Temuri; Gregory Scott McElroy; Ram Prosad Chakrabarty; Lawrence Hsu; Paula M Almonacid; Bryan A Millis; Navdeep S Chandel; Jean-Philippe Cartailler; Vivian Gama
Journal:  Development       Date:  2022-07-06       Impact factor: 6.862

  1 in total

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