Search Results - "Baker, Emma K."

The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia.

Authors: Baker, Emma K. Arora, Sheena Amor, David J. et al.

Source: Journal of Autism & Developmental Disorders. Apr2023, Vol. 53 Issue 4, p1682-1692. 11p. 5 Charts.

Subjects: Child care, Angelman syndrome, Prader-Willi syndrome, Fragile X syndrome, Descriptive statistics, Research funding, Patient care

Geographic Terms: Australia

FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.

Authors: Baker, Emma K. Arpone, Marta Kraan, Claudine et al.

Source: Scientific Reports. 7/16/2020, Vol. 10 Issue 1, p1-8. 8p.

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Authors: Baker, Emma K. Arpone, Marta Bui, Minh et al.

Source: American Journal of Medical Genetics. Part A; Feb2023, Vol. 191 Issue 2, p357-369, 13p

Paternal retraction of a fragile X allele to normal size, showing normal function over two generations.

Authors: Bartlett, Essra Archibald, Alison D. Francis, David et al.

Source: American Journal of Medical Genetics. Part A; Jan2022, Vol. 188 Issue 1, p304-309, 6p

Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Authors: Jarmolowicz, Anna I. Baker, Emma K. Bartlett, Essra et al.

Source: American Journal of Medical Genetics. Part A; May2021, Vol. 185 Issue 5, p1498-1503, 6p

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.

Authors: Baker, Emma K. Arpone, Marta Aliaga, Solange M. et al.

Source: Molecular Autism. 5/3/2019, Vol. 10 Issue 1, pN.PAG-N.PAG. 1p.

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome.

Authors: Kraan, Claudine M Baker, Emma K Arpone, Marta et al.

Source: International Journal of Molecular Sciences. Oct2020, Vol. 21 Issue 20, p7735-7735. 1p.

Epigenetic changes to the MDR1 locus in response to chemotherapeutic drugs.

Authors: Baker, Emma K. Johnstone, Ricky W. Zalcberg, John R. et al.

Source: Oncogene. 12/1/2005, Vol. 24 Issue 54, p8061-8075. 15p. 2 Diagrams, 7 Graphs.

Myelosuppressive Therapies Significantly Increase Pro-Inflammatory Cytokines and Directly Cause Bone Loss.

Authors: Quach, Julie M Askmyr, Maria Jovic, Tanja et al.

Source: Journal of Bone & Mineral Research. May2015, Vol. 30 Issue 5, p886-897.

EphrinB2/EphB4 inhibition in the osteoblast lineage modifies the anabolic response to parathyroid hormone.

Authors: Takyar, Farzin M Tonna, Stephen Ho, Patricia WM et al.

Source: Journal of Bone & Mineral Research. Apr2013, Vol. 28 Issue 4, p912-925.

Methylation of the SLC6a2 Gene Promoter in Major Depression and Panic Disorder.

Authors: Bayles, Richard Baker, Emma K. Jowett, Jeremy B. M. et al.

Source: PLoS ONE. Dec2013, Vol. 8 Issue 12, p1-1. 1p.

A stressed niche not Wnted.

Authors: Baker, Emma K. Purton, Louise E.

Source: Blood. 9/1/2011, Vol. 118 Issue 9, p2377-2378. 2p.

Reply to “Testing for association between MeCP2 and the brahma-associated SWI/SNF chromatin-remodeling complex”.

Authors: Harikrishnan, K. N. Pal, Sharmistha Yarski, Michael et al.

Source: Nature Genetics. Sep2006, Vol. 38 Issue 9, p964-967. 4p.

Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.

Authors: Field, Michael Dudding-Byth, Tracy Arpone, Marta et al.

Source: International Journal of Molecular Sciences. Aug2019, Vol. 20 Issue 16, p3907-3907. 1p. 4 Graphs.