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The inner boundary either goes clockwise, or you put a minus sign.
Narrow apertures at the beginning of cristae of the mitochondrial inner membrane that link cristae to the inner boundary membrane.
The inner boundary membrane that is adjacent to the outer membrane harbors many protein translocases.
Crista junctions form narrow openings that connect the cristae membranes to the inner boundary membrane.
The mitochondrial inner membrane consists of two domains: the folded cristae, which form invaginations, and the inner boundary membrane, which is located adjacent to the mitochondrial outer membrane.
The near-field surface, used to compute the far fields as described above, is along the inner boundary of the PML.
The mitochondrial inner membrane consists of two morphologically distinct domains, the inner boundary membrane and large invaginations termed cristae.
However, previous literatures always neglected the influence of the inner boundary by assuming that it was perfectly adiabatic.
In a reductionist view, cristae shape can be defined by the curvature of two regions: the cristae junctions (CJs), narrow tubular structures connecting cristae to the inner boundary membrane9; and the cristae lumen proper.
In this problem, the location and shape of the inner boundary of a doubly connected domain is unknown.
The inner membrane is divided into two domains: the inner boundary membrane, which is adjacent to the outer membrane, and membrane invaginations termed cristae.
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