inactivation
61Human genetics — describes the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics,… …
62Nav1.4 — Sodium channel, voltage gated, type IV, alpha subunit Solution NMR structure of the IFM motif/inactivation gate of the NaV1.4 sodium channel (PDB 1byy) …
63nervous system — Anat., Zool. 1. the system of nerves and nerve centers in an animal or human, including the brain, spinal cord, nerves, and ganglia. 2. a particular part of this system. Cf. autonomic nervous system, central nervous system, peripheral nervous… …
64SURRÉNALES — Les glandes surrénales furent découvertes en 1543 par B. Eustachi, mais leur rôle n’apparut qu’en 1855 lorsque T. Addison décrivit la maladie bronzée et la rattacha à une destruction de ces glandes. C. E. Brown Séquard (1856) démontra… …
65Ventricular action potential — At rest, the ventricular myocyte membrane potential is about 90 mV, which is close to the potassium reversal potential. When an action potential is generated, the membrane potential rises above this level in four distinct phases.The beginning of… …
66Protein C — Not to be confused with C peptide, C reactive protein, or protein kinase C. Protein C (inactivator of coagulation factors Va and VIIIa) Tertiary structure of human activated protein C (minus the Gla domain …
67Poly ADP ribose polymerase — For the sound, see Parp (onomatopoeic). ADP ribose …
68Neurofibroma — Classification and external resources Histopathologic image of cutaneous neurofibroma obtained by biopsy ICD 10 D36.1 (ILDS D36.160) …
69Insertional mutagenesis — is mutagenesis of DNA by the insertion of one or more bases.[1] Insertional mutations can occur naturally, mediated by virus or transposon, or can be artificially created for research purposes in the lab. Contents 1 Signature tagged mutagenesis 2 …
70Generalized epilepsy with febrile seizures plus — (GEFS+) is a syndromic autosomal dominant disorder where afflicted individuals can exhibit numerous epilepsy phenotypes.[1] GEFS+ can persist beyond early childhood (i.e., 6 years of age). GEFS+ is also now believed to encompass three other… …
