![Ren Hartung](/img/default-banner.jpg)
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Ren Hartung
United States
Registrace 4. 05. 2007
Teaching Positions held:
Full Time Faculty, Glen Oaks Community College 2007 to present
Adjunct Faculty, Kellogg Community College, 2006-2007
Adjunct Faculty, Midlands Technical College, 2002-2006
Clinical background: Medical Assistant 1992-1999, Patient Care Assistant 1991-1994, Navy Hospital Corpsman 1989-1997
Education:
Ph.D., 2006, Biomedical Science, University of South Carolina School of Medicine
Adviser: Dr. Richard Hunt
Dissertation: "Stress Responsive Proteins in the Transformation of Retinal Pigment Epithelium"
B.A., 2000, Anthropology, Albion College
Full Time Faculty, Glen Oaks Community College 2007 to present
Adjunct Faculty, Kellogg Community College, 2006-2007
Adjunct Faculty, Midlands Technical College, 2002-2006
Clinical background: Medical Assistant 1992-1999, Patient Care Assistant 1991-1994, Navy Hospital Corpsman 1989-1997
Education:
Ph.D., 2006, Biomedical Science, University of South Carolina School of Medicine
Adviser: Dr. Richard Hunt
Dissertation: "Stress Responsive Proteins in the Transformation of Retinal Pigment Epithelium"
B.A., 2000, Anthropology, Albion College
Video
How to Clean a Whiteboard like a Professional 24 01 24
zhlédnutí 157Před 6 měsíci
How to Clean a Whiteboard like a Professional 24 01 24
22 08 30 Physiology and interrelationship between Anatomy and Physiology
zhlédnutí 400Před rokem
22 08 30 Physiology and interrelationship between Anatomy and Physiology
22 08 30 List the subdivisions in both microscopic and gross anatomy
zhlédnutí 136Před rokem
22 08 30 List the subdivisions in both microscopic and gross anatomy
22 08 30 Human anatomy Objectives 01 Describe the science of Anatomy
zhlédnutí 129Před rokem
22 08 30 Human anatomy Objectives 01 Describe the science of Anatomy
22 05 26 Blood Typing Kit How to using Eldoncard
zhlédnutí 32KPřed 2 lety
Blood typing done using a "Know Your Blood Type" Eldoncard Home Blood Typing Kit. Done in the Anatomy & Physiology Lab here at Glen Oaks Community College. www.amazon.com/Eldoncard-Blood-Type-Test-Complete/dp/B00JFTSPMW/ref=sr_1_3?keywords=know your blood type kit&qid=1653575190&sprefix=know your blood type,aps,71&sr=8-3
Spinal Cord Models in the Lab and Quiz
zhlédnutí 8KPřed 3 lety
Major parts of the spinal cord models are described including: grey matter (gray matter), central canal, grey commissure, white matter, dorsal horn, ventral horn, lateral horn, dorsal and ventral roots, dorsal root ganglia, spinal nerves, sympathetic trunk.
Clonal Selection Theory for Beginners
zhlédnutí 7KPřed 3 lety
The basics of the clonal selection theory explained... Focusing on B-lymphocytes. with a quiz at the end.
EMG--concepts to understand before lab -- Electromyography -- Muscle Physiology Lab
zhlédnutí 13KPřed 3 lety
EMG concepts to understand before lab Electromyography Muscle Physiology Lab
CAT Scan Sagittal Head
zhlédnutí 836Před 3 lety
Computed tomography (CAT) scan of a human head. A fly through of sagittal sections. Might be useful for discussing sagittal sections or the anatomy observed.
CAT Scan Transverse Head
zhlédnutí 273Před 3 lety
Computed tomography (CAT) scan of a human head. A fly through of transverse sections. Might be useful for discussing transverse sections (transverse planes) or the anatomy observed.
CAT Scan Coronal Head
zhlédnutí 1,6KPřed 3 lety
Computed tomography (CAT) scan of a person's head. A fly through of coronal or frontal sections. Might be useful for discussing coronal sectioning or the anatomy involved. This scan was done specifically to examine the sinuses.
Lymphatic Structures in the Lab
zhlédnutí 5KPřed 3 lety
Going through all of the lymphatic anatomy models that we have at Glen Oaks Community College.
Neuron Model -- parts of the neuron model
zhlédnutí 4,4KPřed 4 lety
The parts of the neuron model are pointed to and described.
Introduction to EMG in the Anatomy and Physiology Lab
zhlédnutí 7KPřed 4 lety
Basic idea of what an EMG is used for in an A&P or Physiology lab.
how the basal nuclei influence motor function
zhlédnutí 637Před 6 lety
how the basal nuclei influence motor function
Reproductive Histology with Study Quiz
zhlédnutí 14KPřed 6 lety
Reproductive Histology with Study Quiz
Urinary System Histology with Study Quiz
zhlédnutí 52KPřed 6 lety
Urinary System Histology with Study Quiz
Renin Angiotensin Aldosterone System System (RAAS)
zhlédnutí 2,1KPřed 6 lety
Renin Angiotensin Aldosterone System System (RAAS)
Positive and Negative Feedback loops and homeostasis
zhlédnutí 72KPřed 6 lety
Positive and Negative Feedback loops and homeostasis
Chemical and Electrical Synaptic Communication
zhlédnutí 23KPřed 6 lety
Chemical and Electrical Synaptic Communication
Levels of Organization of the Human Body
zhlédnutí 9KPřed 6 lety
Levels of Organization of the Human Body
Peripheral Nervous System (PNS) lab models
zhlédnutí 44KPřed 7 lety
Peripheral Nervous System (PNS) lab models
Renin-angiotensin-aldosterone system (RAAS system)
zhlédnutí 8KPřed 7 lety
Renin-angiotensin-aldosterone system (RAAS system)
The phospholipid bilayer, with its fluid mosaic model, is more complex than a basic ceramide. A Ceramide can be a liquid crystal. However, a ceramide can be built up in complexity, constructed synthetically, later adding protein pumps and various changes in areas like electromagnet gradients. To take a chiral liquid crystal molecule and apply a charge to change it into a known state, like a nematic state, would allow a mirror of that on a computer to read the charge or even electron spin for a low count of molecues and then build those up. For instance, like a LCD computer screen, this could be a flat sheet but then a tube can be formed in a flexible screen. A synthetic nerve _(or after that success, an axon, its axoplasm and neuron potentially connected)_ could eventually be made. The simulated computer model would need to react and be proactive as a low-level driver to the physical liquid crystal, mimicking a nerve. Once a tolerance for how many liquid crystals can be placed in the synthetic nerve membrane, organic, biological membranes would need to be made. Then comes the nerve to brain control of an animal similar to a leech or fruit-fly larvae, and then progression to a fruit-fly. That would entail deep-learning, machine-learning _(even trying different graph models over a basic LLM)._ It is at this point when drug-discovery (and LLM computational chemistry) for testing on fruit-fly (larvae, fly and leech) for neurodegenerative diseases _(specifically growing flawed subjects with neurogenerative predispositions over known-quantity genetically predictable time-spans and environmental stimuli for acceleration of neurodegeneration)_ could be applied to accelerate, arrest or even reverse neurodegeneration. These are transactions on neural systems as the basis for the driver. Drug discovery would need to acknowledge endocrine system and hormonal epigenetic effect for deliberately induced neurodegeneration by premature cell death or membrane disruption by RNA interference, or mutation by RNA interference to create a new cell in multiplication by division so that cell copies are less flawed. Also for improving sight-loss, the motor parts of the brain where sight is located also could be studied to change a cell type. This is important because larvae undergo metamorphosis and the fly has the compound eye. A fly can be bred to grow legs for antennae. Then move onto more complex organisms to help write driver interfaces for growing cyber brain interfaces and drivers for axon-neuron learning and improvement in motor unit recruitment _(increasing maximal muscular force)_ in electromyography biomechanics sports, paraplegia, tetraplegia, nerve-damage, Alzheimer's and stroke patients all for rehabilitation engineering _(including prefrontal cortex damage resembling psychopathy)._ The LLM, graph and deep-learning, machine-learning would derive transactions on neural systems to standardise (or consort) in IEEE. So changing blood pH and oxygen content (or carbon monoxide) and simulated altitude training, and electrolytes _(isotonic, solute potential, etc.)_ would be stimuli _(and phantom limb induced by mirror or computer image, and the neuroprosthetic exoskeleton controlled by an epidural electrocorticographic wireless brain-machine interface such as at Institut Carnot)._ The trouble with sensors on muscles is that the best place is in the middle, not by the connective tissue. So to get around this, a synthetic muscle _(starting at chirality which can be defined, per state transition, and Markov state transition, as a spline made up of polynomials, which can be separated into a series by Fourier analysis as per Heisenberg's uncertainty principle for waves and the valence orbitals known)_ and then grown cell type allows a reading to come from anywhere in the muscle. The nematic state and chirality are so much simpler to find a known quantity than the (1972) fluid mosaic model. It would also work in computational chemistry drug discovery for a cell type _(synthetic tissue of eucaryote or procaryote)_ that does not exist but is emulated. As it is IEEE, patient data would be bought including for car and sports injuries and suicide attempts failed since there are no ethics derived for medical data on the technology not yet finalised, and consumer data law is the most concrete where there is not yet the IEEE to describe the medical ethics of what is and what is not private or closed source data. Philanthropy for tax breaks is one avenue. Hospital trains can do some but largely radiation technologies are required in underground or heavily shielded hospitals. Data would most likely need to be sold back to the patients as a licence instance as an NFT or blockchain asset because the polynomial is finite in the cryptographic function so it defines a limit to what the patient data is and how its licence is no longer theirs but of the philanthropic private entity which may include a corporate link. Buying that sort of intimate data from people so soon in rehabilitation, without guarantees of success is fraught with ethics and yet could be their only hope to have mobility and the cell motility. My comment has no hate in it and I do no harm. I am not appalled or afraid, boasting or envying or complaining... Just saying. Psalms23: Giving thanks and praise to the Lord and peace and love. Also, I'd say Matthew6.
Saved Me! So happy to have found you! Excellent voice and great teaching style 💯✨ Looking forward to future studies. Thank you! 🧬😊
My lancet looks nothing like that and my pack doesn't have instructions on it
@@MissGlassButterfly makes me wonder where you bought it from.
This video will 100% save me from my dissection project
Thank you so much. I now know my blood type.
what? we ate these everyday
Thanks alot this have really help me
This is a very helpful video, thank you for taking the time to succinctly explain everything! I’ve taken the eldoncard test twice, and both times I got O Negative
How fo i know if its positive or nagetive?
@@WlisonPhilip of you see clumping in the "anti-D" circle you are Rh positive. If no clumping there, you are Rh negative.
You have helped me in understanding skull structure and number of cranial and facial bones well
Great video Sir! Love it
소도 인간처럼 원초적 공포를 느낀다.
Thank u
Than you❤
Thank you doctor, i watched many videos but yours was very clear and helpful😊 just subscribed!
This model is very very bad for peripheral nerves anatomy! So many mistakes .
Agreed. I do not like these flat models that are trying to be 3D.
thank you for explaining this topic in such a way that's easy to follow and understand.
Very helpful video btw. I wouldn’t have ever gotten the finger pokers off if I hadn’t watched this video.
Thank you Doctor
Thank you boss
This worth Gold! Thanks from Perú.
Great video except that the sound no longer works. I've been using this each quarter of the 23-24 school year and 4th quarter there is no sound.
I just brought that video up on my phone and heard sound... I would share the link with the students abs see if they have trouble hearing it (if that's not what you do already :)
I kinda screwed up my Eldoncard a little bit. I poked myself but I still feel I didn’t put enough blood on the Anti-D circle and the Control circle. I know that I am AB though. But my friend did say that if you look closely, the third circle did react a little, and that means I am Rh positive.
I’m AB+ positive. Probably the weirdest blood type.
Wow
LMAOOO his name is dr. hart and he's dissecting a heart how ironic
The vidio is unable to download
Thanks for the detailed explanation.
What are factors based during selection of lymphocytes,,are all lymphocytes have equal chance of being selected?
thank you 💪
Thank you so much
thank you from China!
How to straighten an EMG curvy baseline, please? I have a green and a red electrode I place on the patient along with a concentric needle
Oh, and thanks for the video. Super helpful
The ureter does not contain a submucosal layer. The layers of the ureter are as follows: Tunica mucosa ( 18:00 lamina epithelialis and 17:45 lamina propria mucosae) then tunica muscularis (stratum longitudinale then circulare then longitudinale) and lastly Tunica adventitia. Therefore a more proper term for the region where you were point would be would be lamina propria mucosae.
looks delicious
@Dr Ren Hartung making it easy-peasy again. A million thanks Sir
Great explanation 😍😍
I messed up my first one I got a new one
Don't feel too bad. I messed up the first three I did :)
Why u gate keeping bro? Inform us
Opps the reproductive organs fell out LOL
WOW a hidden gem! Very clear glad I founfd you. Studying for MBLX helped me so much
رائع جدا🙏🏼🙏🏼🙏🏼
Thank you 🙏
I'm having one done in a few weeks for my peripheral neuropathy. They are expensive!
Thank you
Great explanation thank you 🙏🏼
well, done doctor. thank you.
You’re smart professor!!! Thank you 🙏
I did this today and for some reason it feels normsl