scholarly journals BARISAN JUMLAH BILANGAN PADA BIDANG ALAS SETIAP TINGKAT HEPTAGONAL

Author(s):  
Novelia . . ◽  
Mashadi . . ◽  
Sri Gemawati .
Keyword(s):  

ABSTRACTThe sequence of base plane on the heptagonal is the sum of elements on the base of each heptagonal pyramid level. In this paper will be constructed the form of the base sequence of each heptagonal by using a pattern of sequences formed on the base sequence tetrahedron, pyramid, pentagonal pyramid or hexagonal pyramid.Key words:Sequence of base plane, heptagonal pyramid.ABSTRAKBarisan bidang alas pada heptagonal adalah jumlah bilangan pada alas setiap tingkatpiramida heptagonal. Dalam tulisan ini akan dikonstruksi bentuk barisan alas daripiramida heptagonal dengan menggunakan pola barisan yang terbentuk pada barisanbidang alas tetrahedron, piramida, piramida pentagonal dan piramida hexagonal.Kata kunci:Barisan bidang alas, piramida heptagonal.

Author(s):  
T. A. Welton

An ultimate design goal for an improved electron microscope, aimed at biological applications, is the determination of the structure of complex bio-molecules. As a prototype of this class of problems, we propose to examine the possibility of reading DNA sequence by an imaginable instrument design. This problem ideally combines absolute importance and relative simplicity, in as much as the problem of enzyme structure seems to be a much more difficult one.The proposed technique involves the deposition on a thin graphite lamina of intact double helical DNA rods. If the structure can be maintained under vacuum conditions, we can then make use of the high degree of order to greatly reduce the work involved in discriminating between the four possible purine-pyrimidine arrangements in each base plane. The phosphorus atoms of the back bone form in projection (the helical axis being necessarily parallel to the substrate surface) two intertwined sinusoids. If these phosphorus atoms have been located up to a certain point on the molecule, we have available excellent information on the orientation of the base plane at that point, and can then locate in projection the key atoms for discrimination of the four alternatives.


1991 ◽  
Vol 19 (24) ◽  
pp. 7003-7003 ◽  
Author(s):  
Y. Pommier ◽  
G. Capranico ◽  
A. Orr ◽  
K.W. Kohn

2006 ◽  
Vol 129 (3) ◽  
pp. 320-325 ◽  
Author(s):  
Farhad Tahmasebi

Closed-form direct and inverse kinematics of a new three-degree-of-freedom (DOF) parallel manipulator with inextensible limbs and base-mounted actuators are presented. The manipulator has higher resolution and precision than the existing three-DOF mechanisms with extensible limbs. Since all of the manipulator actuators are base mounted, higher payload capacity, smaller actuator sizes, and lower power dissipation can be obtained. The manipulator is suitable for alignment applications where only tip, tilt, and piston motions are significant. The direct kinematics of the manipulator is reduced to solving an eighth-degree polynomial in the square of the tangent of the half-angle between one of the limbs and the base plane. Hence, there are at most 16 assembly configurations for the manipulator. In addition, it is shown that the 16 solutions are eight pairs of reflected configurations with respect to the base plane. Numerical examples for the direct and inverse kinematics of the manipulator are also presented.


Professor Darlington opened the meeting by challenging us with the view that chromosomes made the laws of heredity, rather than heredity fashioning the organization of chromosomes. To keep this wheel of logic spinning, it may be said that chromosomes also made the process of meiosis and thus determined the laws of meiotic exchange. I choose this gambit because our discussions lent considerable emphasis to the view that chromosome complexity compels its own sets of distinctive, and perhaps varied, mechanisms to effect the ultimate event of molecular recombination. The complexity that leads molecular recombination to operate in elaborate meiotic moulds is not, it should be emphasized, base sequence complexity. On the contrary, sequence repeats and genetic homoeologies, though adding disproportionately little to the base sequence complexity of a genome, adds considerably to the complexity of effecting chromosome alignment and crossing over. How chromosomes of diverse genetic content manage that complexity and in the process mould the characteristics of meiotic behaviour has been the primary target of our deliberations. That no single pattern of meiotic conduct was perceived in consequence of the discussions, is to be expected. To the extent that genomes differ in various aspects of chromosome organization - and that they do is patent - the particulars of meiotic organization might also differ. Although a strong sentiment was occasionally expressed for a single universal process of meiosis, it is my opinion that sameness and universality may be mistakenly treated as synonyms. Universals provide for diversity; they do not impose sameness. The task of identifying universal threads among different meiotic fabrics is not a straightforward one. The ultimate act of genetic recombination offers no detailed guide to the routes by which it may be achieved. Indeed, it is the structure of the chromosome that dictates the route ; recombination only signals the direction.


Biopolymers ◽  
1992 ◽  
Vol 32 (8) ◽  
pp. 1077-1103 ◽  
Author(s):  
Marc Poncin ◽  
Daniel Piazzola ◽  
Richard Lavery

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