A Genetic Edition of William Godwin'sPolitical Justice: MS Abinger c. 24, folios 36r–40v
, 2010 Tom Clucas
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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT A comprehensive synthesis of the broad range of neurodevelopmental and psychiatric manifestations in NF1 is needed to identify knowledge gaps and future directions for NF1 research. In the following scoping review, we identify and summarize the scope of research that examines neurodevelopmental and psychiatric manifestations, both as ...
Meera Chopra +5 more
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The 6th edition of the Science magazine Dance Your Ph.D. contest • Common genetic pathway of Parkinson’sdisease and melanoma • Exploiting bacteriophages for bioscience, biotechnology and medicine conference • Mouse Models of Disease: Using pathology techniques to enhance phenotyping outcomes conference • Publication of HeLa genome and transcriptome causes privacy controversy • The UK proposal to assuage the EU agricultural policies [PDF]
, 2013 Joanna Przybył
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Analysis of Human Genetic Linkage. By J. O
, 2000 Dawn Waterworth
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Australian Journal of Social Issues, EarlyView.ABSTRACT Diagnoses of autism spectrum disorder in Australia have increased considerably in recent years. The current study investigated how the National Disability Insurance Scheme (NDIS) impacts quality of life (QoL) among carers of children with autism spectrum disorder.
Jesse Gerhard, Sharon L. Grant
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The Politics of Framing the Student Problem: Inquiries Into Australian Civics Education, 2006–2024
Australian Journal of Social Issues, EarlyView.ABSTRACT Recurring debates about civics, the kinds of history that should, and should not, be taught in school, and ‘standards debates’ about the ‘basics’ typically follow on the heels of recurring moral panics about the ‘declining’ state of ‘our’ education system.
Patrick O'Keeffe +2 more
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The Clinical Spectrum and Neurodevelopmental Pathogenesis of KPTN‐Related Disorder in a Mouse Model
Annals of Neurology, EarlyView.Objective Pathogenic variants in Kaptin (KPTN) cause KPTN‐related disorder (KRD). KPTN modulates mTOR signaling activation within the KICSTOR complex in response to cellular amino acid levels. We define the clinical spectrum and investigate the developmental pathogenesis of KRD.
Lettie E. Rawlins +104 more
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Modeling the genetic complexity of Parkinson's disease by targeted genome edition in iPS cells
, 2017 Carles Calatayud +3 more
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Reshaping Life: Key Issues in Genetic Engineering, 3rd edition [PDF]
, 2002 Kurt Benirschke
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