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1 stantially among younger women with a linear body type.
2 ent types of dorsal root ganglion (DRG) cell bodies (types 1, 2, 3, and 4), which were previously ide
3 ckground K-channels were abundant in carotid body type-1 cells from wild-type mice and comparable to
5 onis" phenotype, characterized by this ideal body type, and this function could potentially be exploi
10 hemical profile similar to mammalian carotid body Type I (glomus) cells and pulmonary neuroepithelial
11 ontaneously hypertensive rats (SHRs) carotid body type I (glomus) cells exhibit hypersensitivity to c
12 e I cells led us to hypothesize that carotid body type I cells and the apposed nerve endings use diff
13 ngs of the oxygen sensitivity of the carotid body Type I cells are becoming better defined as researc
15 patch clamp technique, isolated rat carotid body type I cells exhibited reversible activation of Cl-
18 The results indicate that, in rat carotid body type I cells, both nicotinic and muscarinic acetylc
19 nsitive and other K+ currents in rat carotid body type I cells, with and without low [Ca2+]o plus hig
21 d-sensitive background K+ channel of carotid body type-I cells is likely to be an endogenous TASK-1-l
22 nsitive background K+ current in rat carotid body type-I cells were investigated and compared with th
25 n concert with the self-selection of certain body types, makes it difficult to identify the individua
26 After adjustment for age, race, childhood body type, parental education, and family CVD history, t
29 n OC burial are strongly influenced by water body type, size, and abundance; land use; and soil and v
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