Science topic
Ear - Science topic
The hearing and equilibrium system of the body. It consists of three parts: the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR. Sound waves are transmitted through this organ where vibration is transduced to nerve signals that pass through the ACOUSTIC NERVE to the CENTRAL NERVOUS SYSTEM. The inner ear also contains the vestibular organ that maintains equilibrium by transducing signals to the VESTIBULAR NERVE.
Questions related to Ear
What explanation or thoughts do you have regarding any change? Brain or ear?
Regarding cervical vestibular evoked myogenic potential (cVEMP), two studies found no difference in latencies or amplitudes between MD and VM patients. However, Taylor et al showed that cVEMP asymmetry ratios for 500 Hz tone bursts were significantly higher for MD than VM. Also they show that the ratio of cVEMP amplitude generated by tone bursts at a frequency of 500 Hz to that generated by 1 kHz was significantly lower for MD affected ears than for VM or controls ears. In concordance, Murofushi et al showed significantly smaller cVEMP amplitudes to 500 Hz tone busts on the affected side of MD.
So what are the standards?
I have ran and reran this PCR so many times and am at a loss for what to do at this point. I started by cutting off a small piece of ear (about the size of rice) using a razor blade and tweezers. I used 70% ethanol spray to sterilize by tools between ears.
I then performed an extraction using chelex beads. 5g of beads in 50mL of nuclease free H2O. I used 100 uL of beads per sample. I used a shaking heater block set at 95C and heated the samples for 40 minutes vortexing every 10 minutes. I then centrifuged the samples for 2 min at 20G. I pipetted off the supernatant leaving the beads and the remaining ear behind.
I then ran a PCR. I used 1x PCR buffer, 1.5mM MgCl2, 0.3 mM DNTP, 0.25 primers, 1U taq, and 1 uL of DNA.
That extraction method didn't seem to be working so I used Platinum Direct PCR Master Mix to extract DNA from the ears. I cut a small 1cm piece of ear and added 20uL of lysis buffer and 0.6uL of Protinease K to each ear. As per the instructions I heated the samples at 98C for 1 min then centrifuged them at 20G for one minute. I pulled off the supernatant and used 2 uL to run a PCR. That seemed to work but I saw lots of high MW products so I centrifuged again at 20G for 20 minutes and ran the PCR again. My bands dissapeared.
So I decided maybe I needed to lyse them for longer. So I repeated the extraction but heated for 30 minutes and centrifuged for 10 minutes. This didn't work and it looked like the DNA was trapped in the wells of the gel. The guide for the kit suggested adding 1uL of Protinease K post PCR. So I used the same DNA and ran another PCR but added protinease K following PCR. This didn't work either.
I am not sure what to do at this point. I have attached the PPT that has all the gels I've run and the conditions.
A 16 year-old male semi-professional swimmer has now presented twice with a left antero-superior tympanic membrane (TM) perforation following a URTI. The perforation is in the same location each time and is slightly larger than a pin hole. This causes him left aural pressure when underwater and a disconcerting squeaking sound in the ear when doing underwater tumble rolls. No otorrhea, tinnitus, hearing loss, vertigo. TM otherwise normal. The right TM is normal. Post-nasal space normal. Non-smoker. No ongoing history suggestive of chronic Eustachian tube (ET) dysfunction.
In the first occurrence, I advised water precautions (ear plug) and observation and it fully healed after 6 weeks. In this occurrence (6 months later) I have advised the same thing and will see him again in about 6 weeks to hopefully confirm healing.
This may be a case of bad luck and will never happen again. However, there is more likely an element of left-sided URTI-related ET dysfunction. Presuming this second perforation heals and perforation recurrence is likely in future, how best to prevent it in this swimmer within whom an intact TM is desirable? Balloon Eustachian tuboplasty? No imaging to date. I'm considering a CT temporal bones.
Hello!
I will set up the DNFB contact hypersensitivity ear swelling model soon, to study the effects of anti-inflammatory agents. As a positive control for reducing the ear swelling reaction, I would like to include dexamethasone in my experiment, for validation of the model.
What is the best way to solve dexamethasone for topical application in mouse contact hypersensitivity? (acetone/olive oil?) Could I use clobetasole as an alternative?
Emergence
Branching
Ear formation
Flowering
Grain filling stage
Dear connection
Kindly let me know when the above stages will start in days
Variety duration- 90 days
Vertigo is a condition that can make it feel like you or your surroundings are spinning, sometimes leading to a loss of balance, according to the U.S. National Library of Medicine.
Coronavirus 2019 or COVID-19 is a novel entity which had led to many challenges among physicians due to its rapidly evolving nature. Vertigo or dizziness has recently been described as a clinical manifestation of COVID-19.
So, Are dizziness and vertigo COVID-19 Symptoms? and why?
Kia ora, I am designing a SELEX protocol to purify a oligonucleotide sequences towards a protein conjugated to magnetic protein G beads. I want to know whether heat elution of specific sequences from the target or chemical elution i.e. using an elution buffer or NaOH, EDTA etc. would be better. I have seen both used in the literature but wonder if anyone would be able to provide any recommendations as well as any papers they found informative.
Thanks for your help,
Rebecca
4 years old boy with unilateral Rt ear microtia and preserved bone conduction ABR waves down to 30 dBHL
The other ear in anatomically and radiologically normal BUT with absent ABR waves for both click and 500 Hz tone burst stimuli.
What is the best line of treatment for this younger kid?
Do you know any technology or a company that provides safe / tight drilling through drinking water aquifers in order to install GHE for shallow geothermal?
Only proven technologies are of our interest!
Hi
I measured brain responses from 20 subjects to 5 different sound stimuli. Stimuli were presented at 3 different intensity levels in one ear at a time. One of the stimuli is like a "standard" and four other stimuli have different characteristics. What I am interested in is to find out which stimuli (of other four) produce a larger response compared to the "standard" stimulus at each intensity level.
I tried to fit mixed model to my data like this:
lme <- lmer(Amp ~ Level*StimType +(1|Subject) +(1|Ear), data = D);
and now I would like to make a multiple comparison and I do it in this way
lsmeans( object=lme, pairwise ~ Level * StimType, adjust= "tukey")
but I just want to compare these four stimuli with the "standard" stimulus at each intensity level, I do not need the comparison between these four stimuli. I can of course ignore them, but is there a more beautiful way to make a comparison I want?
And another question is about the Bonferroni correction. I tried to find information about the necessity of Bonferroni (or Holm, etc.) in mixed models, but I could not find something. Should it be applied? If yes, is it built into the model or should I apply it manually?
Thanks in advance
Best regards
Anna
internode length above the uppermost ear or leaf of the ear or below the ear and if yes, then between which numbers of leaves. Thanks in advance.
Hello friends,
I am currently doing research about the determinants of financial self-sufficiency for moroccan MFIs, I have a data set of 6 individuals and 15 years. I learned that I have to run a Heterogeneity test first. so I am using STATA to do so, But I don't get any results?? I reshaped my data to long format, and declared it as panel data!! I don't know what am I doing wrong, any suggestions?
here's the command :
set more off
local SCR1=0
scalar N=6
scalar T=15
scalar K=7
forvalues i=1/6 {
qui reg OSS OPEX CPB DER EAR PAR30DAYS NAB ALS if i==`i'
local SCR1=`SCR1'+e(rss)
}
di `SCR1'
* Calcul de SCR1C contraint: Estimation sur le modèle empilé
qui reg OSS OPEX CPB DER EAR PAR30DAYS NAB ALS
local SCR1C=e(rss)
di `SCR1C'
*Calcul de la statistique de Fisher F1 N=6 T=15 K=7
local F1=((`SCR1C'-`SCR1')*(N*T-N*(K+1)))/(`SCR1'*(N-1)*(K+1))
*La P_value de F1
di "dof1 = " (N-1)*(K+1) " dof2 = " (N*T-N*(K+1))
local PVF1=Ftail((K+1)*(N-1),(N*T-N*(K+1)),`F1')
* Calcul de SCR1CP: estimation du modèle à effets individuels
xtreg OSS OPEX CPB DER EAR PAR30DAYS NAB ALS ,fe
local SCR1CP=e(rss)
di `SCR1CP'
*Calcul de la statistique de Fisher F2
local F2=((`SCR1CP'-`SCR1')*(N*T-N*(K+1)))/(`SCR1'*(N-1)*K)
*La P_value de F2
di "dof1 = " K*(N-1) " dof2 = " (N*T-N*(K+1))
local PVF2=Ftail(K*(N-1),(N*T-N*(K+1)),`F2')
*Calcul de la statistique de Fisher F3
local F3=(`SCR1C'-`SCR1CP')*(N*(T-1)-K)/(`SCR1CP'*(N-1))
*La P_value de F3
di "dof1 = " (N-1) " dof2 = " (N*(T-1)-K)
local PVF3=Ftail((N-1),(N*(T-1)-K),`F3')
*Affichage des résultats
di in y " SCR1 = " in gr `SCR1'
di in y " SCR1C = " in gr `SCR1C'
di in y " SCR1CP = " in gr `SCR1CP'
di in y "F1 = " in gr `F1'
di in y "F2 = " in gr `F2'
di in y "F3 = " in gr `F3'
di in y "PvalF1 = " in gr `PVF1'
di in y "PvalF2 = " in gr `PVF2'
di in y "PvalF3 = " in gr `PVF3'
Hello,
I'm working on Transport measurement of some material on Si/SiO2 substrate.
I used the photolithography for making align marker and photopad.
To avoid Batman wing(doggy ears), i used LOR 2a and GXR 601 for negative profile and mr-REM 700 remover for lift off
After using LOR2a, i found the weird residue.
So, I cleaned our substrate (already made substrate) again.
but it still remain...
what's wrong ? and how can i remove the residue ?
and if you know how to use the LOR, please tell me.
Thank you
Hello,
I wonder if sound intensity can be more relevant than sound pressure to characterize the acceleration of the tympanic membrane in the ear. Hence, I would like to know if there are some existing work comparing
1. tympanic membrane acceleration,
2. sound pressure at the entrance (or better at different depth) of ear canal,
3. sound intensity at the entrance (or better at different depth) of ear canal.
Some very basic simulations I made with a thin silicone diaphragm seems to indicate that sound intensity is more similar to the diaphragm acceleration as a function of the frequency than the sound pressure, which furthermore suffers from higher variations with insertion depth in the ear canal. However I have a very basic knowledge in acoustic simulation hence my results are not reliable at all and the model is very very far from a realistic ear model. I know there exist a lot of work related to the evaluation of the tympanic membrane acoustic impedance, so maybe a paper where all the parameters needed to make a more realistic simulation would be of great help for me.
Thank you by advance,
Jean
Hello everyone,
I have been told in an informal discussion that some headphones can "have a strong Impact on the HRTF (directional sound incidence on the ear) even though they (averaged over all directions) only marginally influence the sound incidence (which is typically named acoustic transparent)."
I would like to know if there exists some evaluation about the influences that such "acoustic transparant" headphones may have, when weared but not used for sound reproduction, on the localization accuracy of a sound emitted by an external source.
Surely, I am also interested in all contents that may be closely related to this case.
Best regards,
Jean.
How can we implement the 3D Face recognition and 3D Ear Recognition IN MATLAB using .obj image file ?
i am also sending the .obj image file with this question so see the attached file.
I want to measure photosynthesis rate of a wheat ear by IRGA. Which is the most suitable chamber for it? Since its 3 dimensional, how will the area of ear be taken care of
I would like some recommendations on good mice ear puncher. I've been using a scisor model from Braintree, but it never cuts the ear hole off, the tissue always keeps hanging attached to the ear and i have trouble cutting it off to genotype. I contacted someone who sharpens our surgical tools but the guy said they can't properly sharpen those punchers. I need one that properly takes the tissue off the mice's ear so I can use it to genotype. Thanks.
Please help me to identify the disease and its causes, mode of infection and precautions. please look at the attached pictures , skin has corky hard scab type lesions, if remove corky hard layer there is blood under that hard layer. still symptoms are on ears and testis
The male goat of the age about 10 months. weight 43 kg.
Anyone can you hepl me to explian more detail the formulafor wet ear yield estimation.
My formula is grian yield = Grain yield/%SHW*100*0.8,
my question, what is 0.8 and how to come this?
Thanks inadvance,
Some traits like ear leaf area, plant height, grain yield, karnel weight, grain n2 content, nitrate content, chlorophyll content... Any more traits i can take into study???
Technology and the increasing fast trends in globalization have turned the society upside down. The youths are the fast hit in these changing trends. Students in the secondary schools join cult groups, and they perform all initiations attached to the different cult groups. Even when it is their turn to perform the rituals and sacrifices, they donate whoever they want, be it their parents or siblings. Before their people could realize these, things must have been spoilt. There is tremendous moral decay in the society. This is due to lack of censorship in the films, videos and music that the children watch and listen to. Parents and guardians feel less concerned to what pertains to their children and ward's welfare.
One would say that they are doing all these out of youthful exuberance. But any youth that grew up with the fear of God will exhibit limitations in what the person does. How many principals, teachers, or instructors these days try to correct their students who dress improperly and come to school? Take a morning look at students who go to school - The girls in very tight and mini uniforms, the boys in their ass - level trousers pulling below their boxers...This is technology and the changing trends in education.
We have to note that students who come to school naked will end up tomorrow as miscreants in the society. They will dress up as naked people tomorrow either taking drugs or becoming alcoholics, committing one crime or the other . The English adage says, " That a stitch in time saves nine," and "prevention is better than cure."
Youths should be taught the right path to positive living. The boys who wear torn trousers and fry their hair and wear an ear - ring in one ear does not make them either good musicians, international footballers, or even star actors. These looks and attachments make the one look irresponsible and mean.
Women and girls who wear mini - skirts and dresses to seduce and lure men into their debasable trap debase their womanhood and make them worthless before their men.
Indecent dressing is a criminal act, because it can make the seducer and seducee to be in an uncontrollable state to commit crime. The society should correct this trend, because if it is left unchecked, then the next word to be coined after society is "DOOM."
Many studies reported an association between nutrition and human hearing loss. These studies showed the incidence of hearing loss was increased with the lack of micro-nutrients such as vitamins A, B, C, E, zinc, magnesium, selenium and iron.Moreover, high carbohydrate, fat, and cholesterol intake, or lower protein intake, are responsible for poor hearing status.
Dear colleagues, Any more studies or experience about the relation between nutrition and hearing loss?
Hi guys! I want to extract RNA and use it for q_PCR. As it is convenient to collect ear tissue or blood samples from animal so which method will be more efficient to collect RNA from these tissues.
Thanking you in advance.
I have a repeated measures design, looking at how sex hormones effect number of responses on a dichotic listening task, three times over the course of the menstrual cycle.
Where it simply the number of correct responses given by the left ear (LE) or right ear (RE) I wouldn't be stuck, however I'm also looking at voice-onset-time (VOT).
Each question is two dichotically presented consonant-vowel syllables (one LE, the other RE), and each pair is made of a combination of long VOT syllable (delayed onset of the vocal chord vibrations after an unvoiced consonant such as p/ t/ k) and a short VOT (immediate voicing: b/ d/ g) (also short-short and long-long, for a total of 30 combinations - after excluding b+b/d+d etc combinations).
So, the answers I receive are separated out into a wealth of data such as number of correct responses in the left ear from a short-long combination (LE-SL, meaning the short VOT syllable was presented to the left ear, and long to the right) and likewise the number of correct RE responses to the same VOT combination. Or, number of correct responses in the right ear from a short-short combination (RE-SS) etc. (As an aside, I will also have the number a VOT combinations with an incorrect response where neither syllable was correct).
I can then total these aspects to give total number of short VOT-left ear responses etc. So I could now compare means for left-ear-short and left-ear-long, or left-ear-short with right-ear-short.
However, I then have to introduce time into these analyses and I get a bit muddled. Will I have to compare each totalled-response variable separately over the three phases (IV with 3 levels) and so use a repeated measures ANOVA, or is there a way to compare the differences between say short-VOT and long-VOT over three time periods? (attempting to see if a previously demonstrated long-VOT advantage is stable over the course of the menstrual cycle).
This is in SPSS by the way.
Please help, I have bamboozled myself!
Many thanks to any who may offer assistance. (attached is what the collation of responses will look like)
ear colleagues
Laughing style of an individual expresses his/her nation's laughing style, is it right? In other words, laughing style is helpful to describe an individual's ethnicity.
regards
ijaz
Wheat crop experts help me for identification abnormalties.
I would like to measure STI (speech transmission index) in a 3D environment. I have been thinking about use Unity and reproduce the sound from a speaker and record the sound from the character ears but I would like to find something more profesional. All has to be in 3D because the building is not real any more.
Thank you for your time.
I am currently working on a project based on SSVEP. During the data acquisition I am experiencing a consistent peak at 13Hz. And my desired peaks are not very significant in comparison in fft spectrum. I am using electrode positions O1, O2, P3, P4 and FP2. And two reference electrodes on ear lobe. Kindly suggest anything to improve my results. And what should be SNR?
I need to perform a western blot from mice samples, to select positive animals for my experiments. I was thinking of doing western blot from ear tissue, finger or tail. Which one is better?
Thanks
Bacterium does not has nervous system,eyes ,ears and nose still efficiently
As Medical practitioners, we all deal with several patients/people every day.
How many of us are good listeners? And how many us are pushers, pigeon-holing patients swiftly and sometimes erroneously?
Whys are we given two ears but only one mouth?
What are the warning signs and caveats for a superlative physician / doctor?
Can you please show me what feature you think its important and you select it or you just select the standard?
What are the standard?
Thank you in advance.
What causes the abnormal leafy ears in corn?
We have seen this abnormal ears at the end of the season in corn. Usually, at the edges of the field. Not sure about the center of the field (we have not checked).
I have attached pictures for the case.
Thank you in advance for your contribution.
My lab has some mice that we cannot afford to euthanize. We would like to use ear punch biopsies and tail clips for fibroblasts, but I am not sure if there will be enough cells in each to set up a culture. If anyone has had success using ear biopsies and 2-3 mm tail clips for primary cells, could you please share your experience and/or protocols? Thank you!
How can do the 3D Face recognition and 3D Ear Recognition using Deep learning?
Hello,
I'm studying in field condition the F1 vigor of some hybrids of Maize everta in water shortage conditions.
After anthesis I noticed that some plant (without a correlation with the genotype or the treatment) and started to produce ears with masculine trait; some stamen (attached photo).
Since I used to know that usually the flower are imperfect, with ears producing only feminine trait which could be the exogenous cause of this abnormality?
Dears regards,
Ludovico Caracciolo
I have 3D (.obj) image file and i want to do the 3D face and 3D Ear Recognition using python
I am attempting to develop a differential convolution matrix for biometric detection and identification.
which Tool or support package in matlab is good for 3D Face and 3D Ear recognition?
Or just ossicles are the only part that affect amplification?
I think the factors that determine the amplification ratio are the area ratio of tympanic membrane and stapes foot plate, and length ratio of malleus and incus.
Does and surface area of oval window affect amplification ratio?
Do you prefer to use cartilage for reconstruction or bony plate ?
Any available literature regarding this?
thank you I have not read everything yet but that said This is what I am looking for Memory loss , low grade headaches , ringing in ears , thyroid issue suddenly sleeplessness after 2 exposures of Lband 1310 after 9 mins . ( radar )I had a neurologist tell me it was not possible for RF to cause headaches what ever research you can provide would be greatly appreciated . I will try to go threw all references and see if I can find something
i have extracted the DNA from mice ear by NaOH method. some times it works but sometimes doesnt wokr. i used 50um NaOH 100ul . heated at 98 temp for 30 mins. then added 10ul Tris Hcl pH 8. then used 1ul,2,ul,4.4ul in 10ul pcr reaction. first time i got the good results on 4.4ul. but later i did not get result on 4.4 but got the results on 2 ul . i meant to say every time i need to change the volume of the DNA solution for pcr. how can i optimize it.
I work in a primary school and I am struggling with my dissertation as my school are too busy to help. We have a family support worker on site, I want to know what do parents want ? a compassionate listening ear to sound off at, or practical help? What makes a good family support worker?
Thanks
as we know the specific frequency of sound stimulate the specific part of cochlea of ear that was named cilia(hair cells). subsequently ,the cilia convert the amplitude of the sound to corresponding frequency. nevertheless, is the brain sense the rhythm of the sound?
I read a lot of essays saying "research says" with the above figures. I can't find any original research to back this up. It sounds like another misrepresentation of Mehrabian to me, but since I can't find the original source, I'm stuck. Anyone have an idea?
Edit: It started off in a student essay which was properly cited (I clearly taught them well! :) ). However, when I see things like this I always see my old professor shouting *ad fontes* at me. I tried to check up on it in the source cited by my student, but that's where I hit the 'research says' wall. This is in a reputable teaching text book. The search on here and the first twelve pages of Google have yielded only 'research says' and no citations.
I'm really scratching my head over this.
There is scare info on this issue.
Thanks in advance,
Erez
I had Witnessed once ie., my mother poured herbal liguid extract into the ear that cured migraine. What happens there? Extract goes stomach or react with any nerve. what is the exact pathway of poured liquid in ear?
Hi. I am currently working with new materials that should be tested on a scarified skin.
I am employing the widely-accepted wound model using the ventral surface of a rabbit ear, which was originally suggested by professor Mustoe. In brief, this model involves full thickness excision of rabbit ear skin and perichondrium, leaving the bare cartilage to heal itself and form a scar wound.
However, i am having some drawbacks. From some samples, the hypertrophy of the rabbit ear cartilage, rather than the dermal portion, is too prominent. This makes the analysis of the dermal portion very difficult.
My guess is that there had been some random microdamage to the cartilage portion during the removal of the perichondrium, but that leaves me no choice but to leave the perichondrium, which will accelerate the healing and make the wound UN-hypertrophic.
Is there a way to maximally prevent cartilage hypertrophy, but only achieve dermal hypertrophy using this model? Thank You.
Hearing scientists have worked ever so hard in search of physical correlate of pitch in the mechanics or acoustics of sound sources. However, a pitch meter does it so effortlessly. Consider the odds.
Figure 1 presents two waveforms that generate the same musical pitch A3. The two signals were produced by different configurations of a string. The FFT analysis of the two signals are presented in figure 2. The two signals have the same prime component (166 and 165 Hz). The signal (top) has no fundamental but only odd partials, the resonant component is the first in the spectrum. The signal (bottom) is harmonic, but the fundamental (55 Hz) is not present in the signal, and the prime component (165 Hz) is the third partial. Despite these acoustic discrepancies, the ear perceives the same A3 and the pitch meter agrees with it. What does the pitch meter measure to arrive at the pitch A3?
If we could know, the data could offer insights on the principle of the auditory mechanism, and help in preparing hearing aids for sufferers of hearing loss.
It would be a small-scale pilot study using myself as the provider and volunteers as clients. I'm fascinated by reflexology and it's charted indications of active health conditions in clients upon subjective palpation review. I believe the mechanisms of reflexology are similar to that of acupuncture. I'd like to research even elementary connections between the two disciplines. Any constructive advice appreciated.
I am looking for some research on whether it is necessary to pack the ear canal after ear surgery
Please send me any link or references that could be helpful.
I have three gene segments (A,A,B)- note that two of the fragments are identical in sequence. I would like to prepare the following three constructs
AAB, ABA, BAA in pcdna3.0.
I would like to stick with a seamless cloning approach so Gibson came to mind. For those of you that use Gibson, do you see a potential problem by the repeat sequences? If there is a better alternative I am open ears.
Best,
What are the options to reconstruct the outer ear if both superficial temporal arteries are compromised due to the fact that patient has gone through a major craniofacial reconstruction using bi-coronal approach? Patient has the Treacher-Collins syndrome and moderate hypoplasia of zygoma-maxillar complexes. A doppler was made during which has been found a rich posterior occipital vascularisation.
Is it due to changes in the anterior and posterior malleolar ligaments? . Foreshortened handle of malleus is seen in intact drum as well as perforated ear drum.
Earwax composition among Caucasians, among Ethnic Indians of Canada and South America, among Asians and among Indigenous Africans.
Patient has pure tone audiogram showING bilateral hearing within normal limits. Her HRCT Temporal bone shows intact ossicular chain with minimal soft tissue in epitympanum.
She currently has dry ear and no complaints per se..
This is her otoendoscopic picture.
I would like to know if exists a specific methodology to analyse the CoM using 16 markers in the body. In this case, I used four cameras (CODA system) to measure the 3D position, with two markers located on the ear, and the others located on the left and right acromion, anterior superior iliac spine, knee, ankle, fifth metatarsal, elbow, and wrist joints (= 16 markers). What method of analysis I would can use in my research? What method is most indicate with 16 markers?
I'm trying to make contact dermatitis model with FITC/aDBP.
General protocol of model use 20ul 0.5% FITC in vehicle (acetone : DBP = 1:1) per one ear.
The amount FITC in 0.5% of 20ul vehicle is 0.1mg. It's too small amount to measure.
So, I was wondering it is possible to make FITC stock (for example mix with acetone first and store, and before apply to ear mix with DBP)
If anyone who made this FITC/aDBP model, could you give me some advice for me?
I have read many papers and consult several books but one piece of information cannot be found. Imagine normal human ear is exposed to 1 kHz sine sound that causes normal audible loudness of say 40 db. What kind of electrical signals does cochlear send to the brain? If these are electric pulses all of the same shape, height and width, does their shape, height or width relate to the intensity of sound waves and how? If not, what does?
I am looking for detailed anatomical and physiological information about the ear canal. Which kind of receptors are present and how they are distributed along the ear canal? The goal is to find out what one is sensing when a foreign object is placed in the ear canal.
At this time it seems to be so difficult to distinguish the tinnitus causes from a patient to another. While, it is easy to measure accuratly its frequency. The actual instruments can't determine its location along the ear. Is there new technological solutions able to distinguish organic Tinnitus causes?
Despite vascular reasons are well recognized possible causes of sudden hearing loss, I didn' found any report about treatment with low-dose aspiriin in this clinical scenario.
What are the consequences on the speech development? What is the connection with autistic development?
What does the term "contralateral reflex" with respect to the right ear in the case of acoustic stapedial measurements in routine clinical situations mean?
Since there are two different views regarding which ear is to be the stimulus ear and probe ear, please specify.
And while testing reflex decay in the right ear, which contralateral reflex threshold is to be taken?
Is it possible to detect Malassezia bio-film directly in the ear channel? Just to demonstrate that Malassezia is really able to form bio-films in vivo, during infection.
Is there any objective scientific advance or basis?
Is there any condition where the B type tympanogram is present , with the normal ear canal volume (0.48) and thye acoustic relexes are present across the frequencies at 95- 100 dB? ( while the other ear yielded a B type tympanogram -ear canal volume 0.42 with reflexes absent due to middle ear fluid.)
Same size ear ossicles in an adult and a newborn does it maintain the frequency of sound that is perceived?