User profiles for J. J. Cox
James J CoxProfessor of Human Pain Genetics, UCL Verified email at ucl.ac.uk Cited by 9174 |
Sodium channel genes in pain-related disorders: phenotype–genotype associations and recommendations for clinical use
Human studies have firmly implicated voltage-gated sodium channels in human pain
disorders, and targeted and massively parallel genomic sequencing is beginning to be used in …
disorders, and targeted and massively parallel genomic sequencing is beginning to be used in …
Techniques for preventing hypotension during spinal anaesthesia for caesarean section
C Chooi, JJ Cox, RS Lumb, P Middleton… - Cochrane Database …, 2017 - cochranelibrary.com
Background Maternal hypotension is the most frequent complication of spinal anaesthesia
for caesarean section. It can be associated with nausea or vomiting and may pose serious …
for caesarean section. It can be associated with nausea or vomiting and may pose serious …
2001 consensus guidelines for the management of women with cervical cytological abnormalities
TC Wright Jr, JT Cox, LS Massad, LB Twiggs… - Jama, 2002 - jamanetwork.com
ObjectiveTo provide evidence-based consensus guidelines for the management of women
with cervical cytological abnormalities and cervical cancer precursors.ParticipantsA panel of …
with cervical cytological abnormalities and cervical cancer precursors.ParticipantsA panel of …
An SCN9A channelopathy causes congenital inability to experience pain
JJ Cox, F Reimann, AK Nicholas, G Thornton… - Nature, 2006 - nature.com
The complete inability to sense pain in an otherwise healthy individual is a very rare phenotype.
In three consanguineous families from northern Pakistan, we mapped the condition as …
In three consanguineous families from northern Pakistan, we mapped the condition as …
Nurr1 is essential for the induction of the dopaminergic phenotype and the survival of ventral mesencephalic late dopaminergic precursor neurons
…, WD Le, MP Smidt, JJ Cox… - Proceedings of the …, 1998 - National Acad Sciences
Nurr1 is a member of the nuclear receptor superfamily of transcription factors that is
expressed predominantly in the central nervous system, including developing and mature …
expressed predominantly in the central nervous system, including developing and mature …
Hyperphagia, severe obesity, impaired cognitive function, and hyperactivity associated with functional loss of one copy of the brain-derived neurotrophic factor (BDNF) …
The neurotrophin brain-derived neurotrophic factor (BDNF) inhibits food intake, and rodent
models of BDNF disruption all exhibit increased food intake and obesity, as well as …
models of BDNF disruption all exhibit increased food intake and obesity, as well as …
[PDF][PDF] A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome
Human monogenic pain syndromes have provided important insights into the molecular
mechanisms that underlie normal and pathological pain states. We describe an autosomal-…
mechanisms that underlie normal and pathological pain states. We describe an autosomal-…
A homeodomain gene Ptx3 has highly restricted brain expression in mesencephalic dopaminergic neurons
…, C Lanctôt, JJ Tremblay, JJ Cox… - Proceedings of the …, 1997 - National Acad Sciences
The mesencephalic dopaminergic (mesDA) system regulates behavior and movement control
and has been implicated in psychiatric and affective disorders. We have identified a bicoid-…
and has been implicated in psychiatric and affective disorders. We have identified a bicoid-…
A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b
MP Smidt, CHJ Asbreuk, JJ Cox, H Chen… - Nature …, 2000 - nature.com
We identified the LIM homeodomain transcription factor Lmx1b in the mesencephalic
dopamine (mesDA) systems of embryos and adults. Analysis of spatiotemporal expression in …
dopamine (mesDA) systems of embryos and adults. Analysis of spatiotemporal expression in …
Pain perception is altered by a nucleotide polymorphism in SCN9A
F Reimann, JJ Cox, I Belfer… - Proceedings of the …, 2010 - National Acad Sciences
The gene SCN9A is responsible for three human pain disorders. Nonsense mutations cause
a complete absence of pain, whereas activating mutations cause severe episodic pain in …
a complete absence of pain, whereas activating mutations cause severe episodic pain in …