coassembly — noun An assembly that has been assembled in stages, often by different people, from subassemblies … Wiktionary
Generalized 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… … Wikipedia
ITAR — international traffic in arms regulation (coassembly) … Military dictionary
Protein folding — Protein thermodynamics redirects here. For the thermodynamics of reactions catalyzed by proteins, see Enzyme. Protein before and after folding. Protein folding is the process by which a protein structure assumes its functional shape or… … Wikipedia
Achromatopsia — Classification and external resources A person with complete achromatopsia would see only black, white and shades of grey. Additionally, the image would usually be blurry in brighter light (in the brightest light, effectively invisible) but would … Wikipedia
GABAC receptor — protein Name = gamma aminobutyric acid (GABA) receptor, rho 1 caption = width = HGNCid = 4090 Symbol = GABRR1 AltSymbols = EntrezGene = 2569 OMIM = 137161 RefSeq = NM 002042 UniProt = P24046 PDB = ECnumber = Chromosome = 6 Arm = q Band = 14… … Wikipedia
KCNE1 — Potassium voltage gated channel, Isk related family, member 1, also known as KCNE1, is a human gene.cite web | title = Entrez Gene: KCNE1 potassium voltage gated channel, Isk related family, member 1| url =… … Wikipedia
Hypomagnesemia with secondary hypocalcemia — DiseaseDisorder infobox Name = Hypomagnesemia with secondary hypocalcemia Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 602014 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Hypomagnesemia with secondary hypocalcemia (HSH) is an… … Wikipedia
Kir6.2 — is a major subunit of the ATP sensitive K+ channel, an inward rectifier potassium ion channel.cite web | title = Entrez Gene: KCNJ11 potassium inwardly rectifying channel, subfamily J, member 11| url =… … Wikipedia
KvLQT2 — (Kv7.2) is a potassium channel protein coded for by the gene KCNQ2.It is associated with benign familial neonatal convulsions. PBB Summary section title = summary text = The M channel is a slowly activating and deactivating potassium channel that … Wikipedia
