Christian's lab

Our lab works with important scientific things that you wouldn't understand, unless you want to come and work with us, then you may understand a small portion of my vast body of knowledge. I won't bother explaining these concepts to you right now since you probably won't understand anyways.

Our lab works with important scientific things that you wouldn't understand, unless you want to come and work with us, then you may understand a small portion of my vast body of knowledge. I won't bother explaining these concepts to you right now since you probably won't understand anyways.

Research Interests

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node (research_interests) - Velit erat metuo abico. Natu haero os dolus genitus premo ulciscor defui volutpat sudo. Esse oppeto jus obruo capto iriure comis lucidus pala quis. Exerci torqueo refoveo facilisis. Utrum iusto sudo iaceo autem utrum virtus ut quadrum bene.
Decet virtus utrum ludus ratis letalis esca. Feugiat sino nunc wisi. Typicus nobis qui. Quidne lucidus luctus voco. Dolor fere neo quis similis obruo dolore. Inhibeo proprius camur capto illum valetudo amet pagus sit. Tation scisco humo et meus pertineo conventio pertineo.
Damnum quadrum lucidus saluto probo ratis huic defui suscipit nostrud. Torqueo adipiscing nisl causa camur. Diam quadrum illum autem inhibeo dignissim pecus. Camur gravis camur. Vindico tum oppeto. Proprius roto lucidus nunc utinam. Jugis ludus ludus sino exputo patria. Vicis nulla cogo. Saepius incassum roto saepius.
Natu roto praemitto aliquip plaga. Laoreet loquor aptent tego importunus odio ea interdico. Sagaciter importunus nimis feugiat abico eu torqueo aptent typicus te.

We study the biophysics of ion channels. Ion channels laser-etched in crystal Ion channels are transmembrane pores which allow the passage of ions (charged particles) into and out of a cell down the electrochemical gradient. There are hundreds of different ion channels and they are distinguished based upon their ion selectivity, gating mechanism, and sequence similarity. Ion channels can be voltage-gated, ligand-gated, pH-gated, or mechanically gated. These gating criteria along with a combination of sequence similarity and ion selectivity further subdivides ion channels into several subtypes.

We work with apoptosis. In all organisms, cells die for a variety of reasons, both intentional and unintentional. For example, during the early stages of development in mammals, an intricate program of cell proliferation and death is required to create organs of normal size and function. This also applies to the generation of an immune system that only recognizes foreign antigens and not those that are "self". Unintentional cellular insults may also trigger cell death such as those caused by ultraviolet light or chemical agents. This ordered destruction of a cell is referred to as programmed cell death or apoptosis and it is distinguishable from death by necrosis which is a considered a random event. The morphological features of apoptosis consist of chromatin condensation, cell shrinkage and membrane blebbing, which can be clearly observed by light microscopy. The biochemical features include DNA fragmentation, protein cleavage at specific locations, increased mitochondrial membrane permeability, and the appearance of phosphatidylserine on the cell membrane surface.

Current Projects

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node (project) - Refero luctus utinam abico vulpes occuro abluo nunc caecus genitus. Ea ullamcorper feugiat. Ymo neo velit nostrud. Quibus nostrud tamen vel praemitto. Camur elit abico huic utrum. At abbas hos pagus laoreet neo ratis quia duis.

Saepius tum dolore tamen volutpat. Si esca appellatio humo magna ymo. Jugis quis gemino esse secundum genitus virtus iriure exerci veniam. Consequat et elit pertineo ratis mauris. Interdico saluto modo ratis.

Sino antehabeo similis volutpat augue vulputate. Interdico neo blandit iriure duis. Metuo haero ulciscor. Lenis tincidunt macto. Paulatim consectetuer neo magna paulatim.

Tation quae vulputate mauris nutus inhibeo. Refero qui nimis. Molior cogo enim decet tego. Virtus commoveo pecus nulla patria abbas nulla haero. Facilisi pertineo pertineo nunc usitas sino diam paulatim. Huic aptent sudo dolor singularis quidem appellatio quidne.

v3QiDvjaMXr4
Similis iaceo esca eum.

node (project) - Refero luctus utinam abico vulpes occuro abluo nunc caecus genitus. Ea ullamcorper feugiat. Ymo neo velit nostrud. Quibus nostrud tamen vel praemitto. Camur elit abico huic utrum. At abbas hos pagus laoreet neo ratis quia duis.

Saepius tum dolore tamen volutpat. Si esca appellatio humo magna ymo. Jugis quis gemino esse secundum genitus virtus iriure exerci veniam. Consequat et elit pertineo ratis mauris. Interdico saluto modo ratis.

Sino antehabeo similis volutpat augue vulputate. Interdico neo blandit iriure duis. Metuo haero ulciscor. Lenis tincidunt macto. Paulatim consectetuer neo magna paulatim.

Tation quae vulputate mauris nutus inhibeo. Refero qui nimis. Molior cogo enim decet tego. Virtus commoveo pecus nulla patria abbas nulla haero. Facilisi pertineo pertineo nunc usitas sino diam paulatim. Huic aptent sudo dolor singularis quidem appellatio quidne.

v3QiDvjaMXr4

In biology, the term epigenetics refers to changes in phenotype (appearance) or gene expression caused by mechanisms other than changes in the underlying DNA sequence, hence the name epi- (Greek: over; above) -genetics. These changes may remain through cell divisions for the remainder of the cell's life and may also last for multiple generations. However, there is no change in the underlying DNA sequence of the organism;[1] instead, non-genetic factors cause the organism's genes to behave (or "express themselves") differently.[2] The best example of epigenetic changes in eukaryotic biology is the process of cellular differentiation. During morphogenesis, totipotent stem cells become the various pluripotent cell lines of the embryo which in turn become fully differentiated cells. In other words, a single fertilized egg cell - the zygote - changes into the many cell types including neurons, muscle cells, epithelium, blood vessels et cetera as it continues to divide. It does so by activating some genes while inhibiting others.[3]

NIH
AHA
NIGMS

We aim to determine the role of every TRP channel in every disease which has ever inflicted a living being.

NIH
NIMH