Not exact matches
The true testing ground for the implicate - order strategy, it seems to me, may indeed be biology rather than physics, where abstract methods are so powerful as to perhaps make it dispensable: just as the old style building - block materialist was refuted not by philosophical polemic, but by the one authority in which he trusted, i.e., by physics itself, so the nothing - but reductionist in contemporary biology will modify his views should it be possible some day to provide him with a mathematical language that fills the currently existing gap
between our formal knowledge of
gene structure and combinations, and our intuitive apprehension of growth and shape.
Studies on
genes, brain
structures and hormones have failed to identify a clear link
between, on one hand, differences at birth
between the sexes and, on the other, particular behaviour.
His vision of
gene structure was focused on the non-repetitive nature of the code - script, rather than on the relatively simple parallel
between the copying of chromosomes and the ability of crystals to replicate their
structure.
While the authors found evidence for
gene flow
between sampled groups, the ancestral population of Aboriginal Australians started to become
structured around 31» 000 years ago thus creating the genetic diversity observed today.
«It alerts physicians to the relationship
between genes, brain
structure, and behavior,» a relationship that may one day become useful to clinicians.
«The million - dollar question,» Strausfeld says, «would be whether the
genes involved in the development of these
structures are shared
between mouse and fly.
Curiously, this genetic change triggered, millions of years later, the connection
between two
gene regulatory networks (those controlled by ESRP and by Fgfr), which became key for the origin of many vertebrate organs and
structures (lungs, forelimbs and inner ear).
For example, the researchers were able to identify previously unknown
gene expression differences
between the neural stem cells that give rise to the brain's deep
structures versus its neocortical surface, and to show that molecular signatures of different neural cell types arise much earlier in brain development than previously realized.
The team found deep conservation of certain processes that likely reflects similar underlying regulatory processes
between mouse and man, but there were also significant differences in
gene expression during kidney development, as well as in the timing, scale, organization, and molecular profile of key cell types and cell
structures.
Esparza stresses that no one really knows how the differences
between the various subtypes — in the sequence of their env
gene, and
structure of their gp120 — will affect people's immune responses.
With our methods, researchers can answer new questions about the relation
between genes and tissue
structure that was not possible before, which we demonstrate in our paper.
They analysed relationships
between bats, the exact composition of the MHC
genes as well as the molecular
structure of three olfactory receptor
gene families: TAAR2, TAAR3 and TAAR8.
The study also demonstrates an association
between NCAN variations with volumes of certain brain regions in young adults and infants, suggesting that the
gene is able to affect brain
structure and function.
Functional variation in vasopressin 1a receptor
gene structure within and
between vole species predicts behavior Elizabeth Hammock, Center for Behavioral Neuroscience, Emory University, Atlanta, Georga, USA
In a general sense, FP timers can be used in any situation where one wants to understand the relationship
between the age of a cell, protein, or cellular
structure and a particular biological event (trafficking to a subcellular location, start of
gene expression, development of a cell
structure, etc).
For example, it is used to identify correlations
between gene sequences and diseases, to predict protein
structures from amino acid sequences, to aid in the design of novel drugs, and to tailor treatments to individual patients based on their DNA sequences (pharmacogenomics).
The
gene product's precise role is not currently understood but it is thought to anchor regulatory complexes at the photoreceptor connecting cilium, which acts as a bridge
between the inner and outer segments of photoreceptor cells [43] as well as having functions in disk morphogenesis [42] and in the
structure of the ciliary axoneme [44].