Browsing Centre for Genomics and Child Health by Title
Now showing items 792-811 of 835
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Transcriptomic profiling reveals a pronociceptive role for angiotensin II in inflammatory bowel disease.
(Lippincott, Williams & Wilkins, 2024-01-29)Visceral pain is a leading cause of morbidity in inflammatory bowel disease (IBD), contributing significantly to reduced quality of life. Currently available analgesics often lack efficacy or have intolerable side effects, ... -
Transcriptomics of the Prader-Willi syndrome hypothalamus.
(2021)Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder, arising from a loss of paternity expressed genetic material on the imprinted chromosome locus 15q11-q13. Despite increasing clarity on the underlying ... -
Translating molecular advances in Down syndrome and Fragile X syndrome into therapies.
(2018-06)Ongoing treatments for genetic developmental disorders of the central nervous system are mostly symptomatic and do not correct the genetic cause. Recent identification of common mechanisms between diseases has suggested ... -
Transmission of CMV, HTLV-1, and HIV through breastmilk
(Elsevier, 2019-03-14)© 2019 Elsevier Ltd. Breastfeeding is a crucial child survival intervention. However, the potential for transmission of viral infections from mother to child presents the dilemma of how best to interpret the benefits and ... -
Two Cases of BCG Osteomyelitis Diagnosed Through Polymerase Chain Reaction/Electrospray Ionization-Mass Spectrometry Technology.
(Oxford University Press (OUP), 2019-01-07) -
The United Kingdom National Neonatal Research Database: A validation study.
(2018)BACKGROUND: The National Neonatal Research Database (NNRD) is a rich repository of pre-defined clinical data extracted at regular intervals from point-of-care, clinician-entered electronic patient records on all admissions ... -
The United Kingdom's global health funding cuts will exacerbate inequities.
(2021-04-12)To the Editor