000 02287ngm a2200409 a 4500
001 HST3660
003 UkLoHST
006 m c
007 cr|cna|||a||||
007 vz|czazum
008 141027s2014 enk|||||||||||s|||v|eng d
028 5 0 _a3660
_bHenry Stewart Talks
035 _a(UkLoHST)2893
040 _aUkLoHST
_beng
_cUkLoHST
100 1 _aWoods, Geoff,
_u(University of Cambridge, UK)
_4spk
245 1 0 _aCongenital syndromes of pain and painlessness
_h[electronic resource] /
_cGeoff Woods.
260 _aLondon :
_bHenry Stewart Talks,
_c2014.
300 _a1 online resource (1 streaming video file (57 min.) :
_bcolor, sound).
490 1 _aMolecular genetics of human disease,
_x2056-452X
500 _aAnimated audio-visual presentation with synchronized narration.
500 _aTitle from title frames.
505 0 _aContents: What is pain? -- How much pain is someone suffering? -- What is the use of pain? -- Pain pathways -- Types of pain (Nociceptive, Inflammatory, Neuropathic, mixed) -- Primary erythromelalgia -- Mutations in SCN9A cause erythromelalgia -- Voltage-gated ion channels -- Paroxysmal extreme pain disorder (familial rectal pain) -- Mutations in SCN9A cause PEPD -- Congenital insensitivity to pain -- SCN9A gene map -- Electrical activity of wild type versus mutant constructs -- Low-copy number vector = pcDNA3JC -- Exon 6 splice variants -- Neuropathies HSANs -- Rita Levi Montalcini -- TRKA signalling -- Hereditary autonomic and sensory neuropathy type 4 (HSAN4) -- HSAN5 -- NGFB -- Familial dysautonomia -- Treatment of pain -- Mendelian disorders of pain.
506 _aAccess restricted to subscribers.
538 _aMode of access: World Wide Web.
650 0 _aCongenital insensitivity to pain.
650 0 _aGenetic disorders.
650 0 _aPain.
650 2 _aDysautonomia, Familial.
650 2 _aErythromelalgia.
650 2 _aHereditary Sensory and Autonomic Neuropathies.
650 2 _aPain Insensitivity, Congenital.
650 2 _aPain.
650 2 _aParoxysmal Extreme Pain Disorder.
830 0 _aHenry Stewart talks.
_pBiomedical & life sciences collection.
_pMolecular genetics of human disease.
856 4 0 _uhttps://hstalks.com/bs/2893/
856 4 2 _uhttps://hstalks.com/bs/p/810/
_3Series
999 _c76992
_d76992