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Emma K Baker

Showing results (41-50 of 57) with videos related to

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Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.
The American Journal of Pathology|December 14, 2011
A novel population of cells expressing both hematopoietic and mesenchymal markers is present in the normal adult bone marrow and is augmented in a murine model of marrow fibrosisMasanobu Ohishi, Wanida Ono, Noriaki Ono, et al.
Research in Developmental Disabilities|September 30, 2022
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disordersMarta Arpone, Lesley Bretherton, David J Amor, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
International Journal of Molecular Sciences|October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X SyndromeClaudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A|September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generationsEssra Bartlett, Alison D Archibald, David Francis, et al.
Bone|March 15, 2013
Modeling distinct osteosarcoma subtypes in vivo using Cre:lox and lineage-restricted transgenic shRNAAnthony J Mutsaers, Alvin J M Ng, Emma K Baker, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
American Journal of Medical Genetics. Part A|November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndromeEmma K Baker, Marta Arpone, Minh Bui, et al.
Scientific Reports|July 18, 2020
FMR1 mRNA from full mutation alleles is associated with ABC-C<sub>FX</sub> scores in males with fragile X syndromeEmma K Baker, Marta Arpone, Claudine Kraan, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.
The American Journal of Pathology|December 14, 2011
A novel population of cells expressing both hematopoietic and mesenchymal markers is present in the normal adult bone marrow and is augmented in a murine model of marrow fibrosisMasanobu Ohishi, Wanida Ono, Noriaki Ono, et al.
Research in Developmental Disabilities|September 30, 2022
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disordersMarta Arpone, Lesley Bretherton, David J Amor, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
International Journal of Molecular Sciences|October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X SyndromeClaudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A|September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generationsEssra Bartlett, Alison D Archibald, David Francis, et al.
Bone|March 15, 2013
Modeling distinct osteosarcoma subtypes in vivo using Cre:lox and lineage-restricted transgenic shRNAAnthony J Mutsaers, Alvin J M Ng, Emma K Baker, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
American Journal of Medical Genetics. Part A|November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndromeEmma K Baker, Marta Arpone, Minh Bui, et al.
Scientific Reports|July 18, 2020
FMR1 mRNA from full mutation alleles is associated with ABC-C<sub>FX</sub> scores in males with fragile X syndromeEmma K Baker, Marta Arpone, Claudine Kraan, et al.
Pageof 6