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Translational Psychiatry
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April 24, 2018
Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism
Clare L van Eyk, Mark A Corbett, Alison Gardner, et al.
Life Science Alliance
|
August 24, 2019
Heterozygous loss of function of <i>IQSEC2</i>/<i>Iqsec2</i> leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females
Matilda R Jackson, Karagh E Loring, Claire C Homan, et al.
Children & Society
|
May 23, 2022
The unequal impact of Covid-19 on the lives and rights of the children of modern slavery survivors, children in exploitation and children at risk of entering exploitation
Erika Jiménez, Vicky Brotherton, Alison Gardner, et al.
Cell Chemical Biology
|
May 12, 2023
Human nuclear hormone receptor activity contributes to malaria parasite liver stage development
Nimisha Mittal, Chadwick Davis, Peter McLean, et al.
European Journal of Human Genetics : EJHG
|
February 23, 2012
Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations
Michael Field, Ingrid E Scheffer, Deepak Gill, et al.
Equine Veterinary Journal
|
August 21, 2021
Acute abdominal dehiscence following laparotomy: A multicentre, international retrospective study
Michelle J Hann, Tim S Mair, Alison Gardner, et al.
European Journal of Medical Genetics
|
October 27, 2019
EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities
Marie Shaw, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, et al.
Molecular Psychiatry
|
March 7, 2024
Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway
Rebekah de Nys, Alison Gardner, Clare van Eyk, et al.
Human Mutation
|
May 9, 2020
Constraint and conservation of paired-type homeodomains predicts the clinical outcome of missense variants of uncertain significance
Monica H N Thai, Alison Gardner, Laura Redpath, et al.
European Journal of Medical Genetics
|
June 13, 2017
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations
Mark A Corbett, Samantha J Turner, Alison Gardner, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 54) with videos related to
Sort By:
Page
of 6
Translational Psychiatry
|
April 24, 2018
Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism
Clare L van Eyk, Mark A Corbett, Alison Gardner, et al.
Life Science Alliance
|
August 24, 2019
Heterozygous loss of function of <i>IQSEC2</i>/<i>Iqsec2</i> leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females
Matilda R Jackson, Karagh E Loring, Claire C Homan, et al.
Children & Society
|
May 23, 2022
The unequal impact of Covid-19 on the lives and rights of the children of modern slavery survivors, children in exploitation and children at risk of entering exploitation
Erika Jiménez, Vicky Brotherton, Alison Gardner, et al.
Cell Chemical Biology
|
May 12, 2023
Human nuclear hormone receptor activity contributes to malaria parasite liver stage development
Nimisha Mittal, Chadwick Davis, Peter McLean, et al.
European Journal of Human Genetics : EJHG
|
February 23, 2012
Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations
Michael Field, Ingrid E Scheffer, Deepak Gill, et al.
Equine Veterinary Journal
|
August 21, 2021
Acute abdominal dehiscence following laparotomy: A multicentre, international retrospective study
Michelle J Hann, Tim S Mair, Alison Gardner, et al.
European Journal of Medical Genetics
|
October 27, 2019
EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities
Marie Shaw, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, et al.
Molecular Psychiatry
|
March 7, 2024
Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway
Rebekah de Nys, Alison Gardner, Clare van Eyk, et al.
Human Mutation
|
May 9, 2020
Constraint and conservation of paired-type homeodomains predicts the clinical outcome of missense variants of uncertain significance
Monica H N Thai, Alison Gardner, Laura Redpath, et al.
European Journal of Medical Genetics
|
June 13, 2017
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations
Mark A Corbett, Samantha J Turner, Alison Gardner, et al.
Page
of 6