Re: [Histonet] [EXT] Histonet Digest, Vol 215, Issue 16

2021-10-22 Thread Huynh,Thomas via Histonet
Hello Administrator,

I would like to ask if it is okay or allow to post jobs on the histonet site? I 
have a friend who is in desperate need of help.

Thanks,

Thomas


Thomas Huynh, BS, HT(ASCP) CM
Chief Histology Laboratory
Department of Veterinary Medicine & Surgery
UT MD Anderson Cancer Center
1515 Holcombe Unit 063
thu...@mdanderson.org
T 713-745-5077 Lab 713-792-2793
C 832-794-0741



True Colors: Gold


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[Histonet] Zebra Fish Histology Protocol

2021-03-26 Thread Huynh,Thomas via Histonet
Good morning Histonetters,

Happy Friday! Does anyone has a zebra fish histology protocol who willing to 
share with me? From fixation, decalcifying, embed to cutting.

Thank you in advance.

Thomas

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[Histonet] Shandon Varistain Gemini Slide Stainer

2016-06-23 Thread Huynh, Thomas via Histonet
Hi All,
Does anyone know the life expectancy of the Gemini H stainer? My boss has 
asked me this question because we are in the process of requesting for a new 
one.

Thomas

Thomas Huynh   BS, HT (ASCP)
Histology Lab Supervisor |Department of Pathology
HARRISHEALTH SYSTEM
5656 Kelly Street
Houston, Tx 77026
Lyndon B. Johnson General Hospital (LBJGH)
O: 713.566.5282 | F: 713.566.5285 | P: 713.297.1606 |
thomas.hu...@harrishealth.org

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[Histonet] Decalcification

2015-07-20 Thread Huynh,Thomas via Histonet
Hello Histoneters,

I would like to add that washing after decalcifying is still not enough. The 
bone specimens have to be neutralized before processing ( putting them in the 
neutralizer solution), so there are no trace of acid when we process them.

Thomas 


-Original Message-
From: histonet-requ...@lists.utsouthwestern.edu 
[mailto:histonet-requ...@lists.utsouthwestern.edu] 
Sent: Monday, July 20, 2015 12:00 PM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 140, Issue 22

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Today's Topics:

   1. Decalcification (Steve McClain)
   2. Cerner PathNet AP tracking (Younes, Pamela S)


--

Message: 1
Date: Sun, 19 Jul 2015 19:00:38 +
From: Steve McClain ste...@mcclainlab.com
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Subject: [Histonet] Decalcification
Message-ID: d1120672-3c80-47aa-b578-85523b3c9...@mcclainlab.com
Content-Type: text/plain; charset=us-ascii

One frequently overlooked point is washing after decal. Especially important 
with acid decal, we wash for an hour in running water. 


--

Message: 2
Date: Mon, 20 Jul 2015 13:00:06 +
From: Younes, Pamela S pamela.s.you...@uth.tmc.edu
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Subject: [Histonet] Cerner PathNet AP tracking
Message-ID:
d9c344263273d74b870b35a54a88ba5a04367...@uthmail2.uthouston.edu
Content-Type: text/plain; charset=iso-8859-1

Hello everyone,
Has anyone used the Cerner PathNet AP tracking system? I would like to hear 
about any feedback, good or bad.
Many thanks,
Pam Younes

Pamela S. Younes MHS, HTL(ASCP), CPC(AAPC), PA(ASCP) Pathologists' Assistant 
Assistant Professor, Department of Pathology and Laboratory Medicine University 
of Texas Medical School, Houston
6430 Fannin, MSB 2.233
Houston, TX 77030
(713) 704-2053



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[Histonet] Microwave Decalcification

2015-05-22 Thread Huynh,Thomas
Hi Kimberly,

We are currently using the Milestone Medical brand microwave to decalcify 
our bone marrow core biopsies. After fixation we decal the core biopsies in the 
microwave for 2.5 hours at 50 degree Celsius with the 10% Formic Acid (we made 
up the formic acid in-house). If you need more info please email me.

Thanks 

Thomas  

-Original Message-
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[mailto:histonet-requ...@lists.utsouthwestern.edu] 
Sent: Friday, May 22, 2015 12:00 PM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 138, Issue 26

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Today's Topics:

   1. Microwave Decalcification (Kimberly Marshall)
   2. Donating Old Microtome (Heather Marlatt)
   3. Re: Donating Old Microtome (Liette Tougas)
   4. Re: Donating Old Microtome (John Kiernan)
   5. Buying service contracts (Johnson, Carole)
   6. Re: Buying service contracts (Morken, Timothy)


--

Message: 1
Date: Thu, 21 May 2015 17:25:04 +
From: Kimberly Marshall kimbe...@animalreferencepathology.com
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Subject: [Histonet] Microwave Decalcification
Message-ID: 1432229164867.39...@animalreferencepathology.com
Content-Type: text/plain; charset=iso-8859-1

?Can anyone that has used the microwave decalcification method, please let me 
know how it worked for you?  Thanks in advance.


Kimberly



Kimberly Marshall H.T.(ASCP)

Histology/Lab Supervisor

Toll Free 1-800-426-2099

Fax 801-584-5104

PO Box 17580

Salt Lake City, Utah 84107

www.animalreferencepathology.comhttp://www.animalreferencepathology.com/



Advancing the art and science of veterinary medicine



[cid:image001.jpg@01CF8F87.A0BD4830]



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Message: 2
Date: Thu, 21 May 2015 12:49:48 -0700
From: Heather Marlatt hmarlat...@gmail.com
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Subject: [Histonet] Donating Old Microtome
Message-ID:
calavvk5jqsaf1b99eo0mxhjck4acgukqd+pkcnzsm_txzvn...@mail.gmail.com
Content-Type: text/plain; charset=UTF-8

I'm posting on behalf of a local researcher. They have been using an older 
microtome that was previously donated by a hospital. It broke down recently and 
they cant afford to replace it right now. It is used by the students to cut 
their own sections so they just need something that can section at 4 microns. 
They are happy to pay the freight if anyone out there has an old working 
microtome that they are willing to donate.

Thank you!!!

Heather


--

Message: 3
Date: Fri, 22 May 2015 03:24:09 +
From: Liette Tougas ltou...@dawsoncollege.qc.ca
To: Heather Marlatt hmarlat...@gmail.com,
histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Donating Old Microtome
Message-ID:
455897b94cf3a44f81f727160f23fb11640c5...@dc229.ad.dawsoncollege.qc.ca

Content-Type: text/plain; charset=iso-8859-1

Hi Heather, 

I do not know where you are located but we have 5-6 good old AO microtomes that 
still work very well that we are willing to donate.  They are in excellent 
condition as they were extremely well maintained over the years and, as a 
Biomed Lab technology teaching department, they have been used only twice a 
week for 3 weeks each fall semester since they were purchased, some 30 years 
ago!  They each have a disposable blade holder (high profile) and block clamp 
(vs original screwing block holder).  We easily cut at 4 microns on them. The 
offer is opened to anyone who can pick them up or pay for shipment.  

Liette Tougas, RT, B.Sc., M.Sc.
Biomedical Laboratory Technology Department Dawson College, Montr?al, Qc, 
Canada 514-931-8731, ext 1519 
From: Heather Marlatt [hmarlat...@gmail.com]
Sent: May 21, 2015 3:49 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Donating Old Microtome

I'm posting on behalf of a local researcher. They have been using an older 
microtome that was previously donated by a hospital. It broke down recently and 
they cant afford to replace it right now. It is used by the students to cut 
their own sections so they just need something that can section at 4 microns. 
They are happy to pay the freight if anyone out there has an old working 
microtome that they are willing to donate.

Thank you!!!

Heather

[Histonet] Bone Station- Milestone

2014-12-16 Thread Huynh,Thomas
Hi Joana,

We are currently using the Milestone microwave to decal our bone marrow core 
biopsies (for faster TAT).  We use our in-house formic acid (10%) and run it in 
the microwave for 2.5 to 3.00 hours with 50 degree Celsius cycle (you can tweak 
to where it works for your specimens). Assuming that they have been fixed well 
prior to decalcifying; personally, I would rather decal them the old fashion 
overnight but they always rush them nowadays. 

Thomas  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
histonet-requ...@lists.utsouthwestern.edu
Sent: Sunday, December 14, 2014 12:02 PM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 133, Issue 16

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Today's Topics:

   1. BoneSTATION - Milestone (Joana Moreira)


--

Message: 1
Date: Sun, 14 Dec 2014 04:36:44 +
From: Joana Moreira jmore...@sidra.org
Subject: [Histonet] BoneSTATION - Milestone
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:
a478ef23b3aad44cad6804356d5676bb02ebd...@mv3wexmx03prv.smrc.sidra.org

Content-Type: text/plain; charset=iso-8859-1

Hi everyone!

I was wondering if there's anyone out there using the Milestone BoneSTATION for 
fixing and decalcifying bone tissue: 
http://www.milestonemedsrl.com/histopathology/products/pre-analytical-tools/bonestation.html
Is it good? Not good?
Easy to operate and maintain?
Do you use it with in-house decalcifying solutions or commercial available ones?
Have you tried their MOL-Decal solution on BMT? Any thoughts?
What about the optimization and standardization of protocols? Is it quite 
straight forward? Or complicated / Difficult?

We are considering it and any feedback would be much appreciated. Send me a PM 
if you like.

Many Thanks,
Joana

Joana Moreira
Supervisor - Anatomical Pathology
Department of Pathology

Sidra Medical  Research Center
PO Box 26999 | Doha, Qatar
Direct Line  +974-4404-2036
jmore...@sidra.org | www.sidra.org





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[Histonet] RE: Decalcifying and Processing large bone

2014-08-06 Thread Huynh,Thomas
Hi Bret
We are using 10% Formic Acid as well and checking the decalcifying end-point by 
using the faxitron x-ray system. I work with bone cancer for 99% of the time 
and Formic Acid is safer than any other one.

Thomas 

-Original Message-
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[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
histonet-requ...@lists.utsouthwestern.edu
Sent: Wednesday, August 06, 2014 10:13 AM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 129, Issue 6

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Today's Topics:

   1. RE: Protocol for decalcifying and processing large bone
  section. (DiCarlo, Margaret)
   2. AW: [Histonet] RE: whole slide scanners (Gudrun Lang)
   3. Glassware Cleaning, CAP Checklist Item GEN.41770 (Laurie Colbert)
   4. RE: RE: whole slide scanners (Elizabeth Chlipala)
   5. Listservers in microbiology (Jorge A. Santiago-Blay)
   6. AW: [Histonet] RE: whole slide scanners (Gudrun Lang)
   7. Procedures and Policy manual needed (Dr. Max Mirot)
   8. RE: Glassware Cleaning, CAP Checklist Item GEN.41770
  (Cooper, Brian)
   9. RE: RE: whole slide scanners (Morken, Timothy)
  10. RE: Listservers in microbiology (Cartun, Richard)
  11. RE: RE: whole slide scanners (James Watson)
  12. RE: RE: Glassware Cleaning, CAP Checklist Item GEN.41770
  (Joelle Weaver)
  13. RE: RE: Glassware Cleaning, CAP Checklist Item GEN.41770 (Jamal)
  14. Re: Protocol for decalcifying and processing large bone
  section. (Barry Rittman)
  15. Re: RE: Glassware Cleaning, CAP Checklist Item GEN.41770
  (Michael Ann Jones)
  16. RI company seeks plastics company for research work
  (Hans B Snyder)
  17. p16 (sarah.dys...@stdavids.com)
  18. neutralize formalin (Mary Ann Deathridge)


--

Message: 1
Date: Tue, 5 Aug 2014 17:01:16 +
From: DiCarlo, Margaret mdica...@kaleidahealth.org
Subject: RE: [Histonet] Protocol for decalcifying and processing large
bonesection.
To: 'Clough, Bret' clo...@medicine.tamhsc.edu, Histonet list serv.
histonet@lists.utsouthwestern.edu
Message-ID:

731be09cdb19aa43aa8682199d42d31b1dc79...@adcexchange01.kaleidahealth.org

Content-Type: text/plain; charset=us-ascii

I use 10% formic acid for large human bones but I don't think your bone 
sections are that large.

Peggy DiCarlo
Ortho Bone Lab
BGMC
100 High St. 
Buffalo, NY  14203

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Clough, Bret
Sent: Tuesday, August 05, 2014 11:55
To: Histonet list serv.
Subject: [Histonet] Protocol for decalcifying and processing large bone section.

Hi everyone,
 I was hoping someone on histonet would being willing to help me by either 
sharing their protocol or advising me on decalcifying and processing large bone 
sections. The bone sections are from the femural head of sheep measuring 
roughly 1cm x 1 1/2 cm cube.  Currently I've been decalcifying the samples in 
0.5M EDTA which is taking along time to decalcify this being the 19th day.  Any 
advise would be greatly appreciated!


Sincerely,
   Bret Clough
   Texas AM Health Science Center
   Temple, TX.
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The Keeping You Informed section of Kaleida Health`s website features a wealth 
of information, stories and pictures about our valued workforce and the 
tremendous momentum our organization is experiencing. Check us out at: 
www.kaleidahealth.org/kyi

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[Histonet] Moh's Job

2014-02-18 Thread Huynh,Thomas
Hello everyone in the Histoland

I am posting a job for a friend; they are looking for a fulltime Mohs' tech at 
a local dermatology practice in the Houston Texas Medical Center. Please 
contact Ms. Stephanie Huff at 281-799-0521.

Thomas



Thomas Huynh HT(ASCP)
Dept. of Pathology
Histology/ Bone Lab
Tel. 713-745-4759
Fax. 713-792 2046


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[Histonet] Powerpath QA

2013-09-25 Thread Huynh,Thomas
Ms. McCaig

We are using it for quite some time; it is not the best out there but if you 
can contact me, I would be able to go into detail further.



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
histonet-requ...@lists.utsouthwestern.edu
Sent: Wednesday, September 25, 2013 10:53 AM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 118, Issue 43

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Contents of Histonet digest...


Today's Topics:

   1. Submitting Questions (Joanne Clark)
   2. ER/PR results tracking (Clare Thornton)
   3. RE: Submitting Questions (Nails, Felton)
   4. Ceramide antibodies (Mark Elliott)
   5. RE: RE: Submitting Questions (Douglas Porter)
   6. Article: Anatomic Pathology Takes a Leap in Quality Process
  Improvement (Judy O'Rourke)
   7. Re: Histonet Digest, Vol 118, Issue 42 (Mark Elliott)
   8. RE: Submitting Questions (Martha Ward-Pathology)
   9. RE: RE: Submitting Questions (pru...@ihctech.net)
  10. PowerPath QA (Diana McCaig)
  11. Ventana Vantage and PowerPath (Victor A. Tobias)
  12. RE: ER/PR results tracking (Cartun, Richard)
  13. RE: Peggy Wenks award (Tony Henwood (SCHN))
  14. Re: RE: Peggy Wenks award (David Kemler)
  15. RE: edge effect on IHC (Tim Higgins)
  16. Re: edge effect on IHC (Jan Shivers)
  17. Re: RE: Peggy Wenks award (Jackie Lair)
  18. Re: RE: Submitting Questions (nancy lowen)


--

Message: 1
Date: Tue, 24 Sep 2013 17:53:56 +
From: Joanne Clark jcl...@pcnm.com
Subject: [Histonet] Submitting Questions
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:
0494a7d4e8cc254ea2fb81464982e378b4aba...@s10maild001n3.sh10.lan
Content-Type: text/plain; charset=us-ascii

Can anyone out in histoland explain to me why my submitted questions are not 
making it through to histonet?  I submitted a question on the 19th of 
September, and I still have not seen it appear in the group emails I get daily. 
 I sent the question to the correct address (I checked it to be sure).  When I 
respond to someones question, I can see my responses, I just can't seem to get 
an original question submitted.  Can anyone tell me what I am doing wrong?




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Message: 2
Date: Tue, 24 Sep 2013 14:40:15 -0400
From: Clare Thornton cthorn...@dahlchase.com
Subject: [Histonet] ER/PR results tracking
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:
c9d78ffc9d668b4cbea4405f84697504013d67ac1...@iris.dahlchase.net
Content-Type: text/plain; charset=us-ascii

How is everyone tracking their ER/PR results to comply with the following:


ANP.22970


Annual Result Comparison


Phase I




For immunohistochemical and FISH/ISH tests that provide independent predictive 
information, the laboratory at least annually compares its patient results with 
published benchmarks, and evaluates interobserver variability among the 
pathologists in the laboratory.

NOTE: Individuals interpreting the assay must also have their concordance 
compared with each other and this concordance should also be at least 95%.

With specific reference to estrogen and progesterone receptor studies: in 
general, the overall proportion of ER-negative breast cancers (invasive and 
DCIS) should not exceed 30%. The average is somewhat lower in postmenopausal 
than premenopausal women (approximately 20% vs. 35%). The average is 
considerably lower in well-differentiated carcinomas (10%) and certain special 
types of invasive carcinomas (10% in lobular, tubular, and mucinous types). 
The proportion of PgR-negative cases is 10-15% higher than for ER in each of 
these settings. Investigation is warranted if the proportion of negative cases 
is significantly higher in any of these settings.



Our LIS doesn't have an easy way of compiling these results.  Basically, we are 
stuck with searching 

[Histonet] RE: Decalcifying bone

2012-07-25 Thread Huynh,Thomas
  Ms. Clark
We are currently use 10% formic Acid in a microwave oven to decal ours for 
about 2 and 1/2 hour after they were fix in 10% neutral buffer Formalin. We 
were told that they are Ok for immuno-stains.

Thomas Huynh, HT( ASCP)
Clinical Histology Technician
Pathology/ Histology/ Bone Lab
thu...@mdanderson.org
T 713-745-4759
F 713-792-2046


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
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Sent: Wednesday, July 25, 2012 12:01 PM
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Subject: Histonet Digest, Vol 104, Issue 30

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Today's Topics:

   1. Decalcifying bone (Jeanne Clark)
   2. Re: RE: Secondary antibody causing nuclear staining (Eva Permaul)
   3. Thank you for coverslipper responses (Brendal Finlay)
   4. CAP Sample Exchange Registry (jgold...@bidmc.harvard.edu)
   5. Re: Markers for Rat Samples (Hobbs, Carl)
   6. Thanks for all the good wishes (Louise Renton)


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Message: 1
Date: Wed, 25 Jul 2012 07:14:06 -0700 (PDT)
From: Jeanne Clark paintedsplas...@yahoo.com
Subject: [Histonet] Decalcifying bone
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
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1343225646.39594.yahoomail...@web161703.mail.bf1.yahoo.com
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In looking through old procedures, I have found several different 'solutions' 
that have been used for fixation and decalcification of bone (particularly bone 
marrow cores). ?I would very much appreciate hearing what people are using 
today for optimal fixation and decalcification of bone for routine pathology 
and IHC testing.


Thank you,

Jeanne Clark
Histology/IHC
Stanford Hospital and Clinics

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Message: 2
Date: Wed, 25 Jul 2012 10:59:58 -0400
From: Eva Permaul e...@georgetown.edu
Subject: Re: [Histonet] RE: Secondary antibody causing nuclear
staining
To: Reynolds, Donna M dreyn...@mdanderson.org,  histonet
histonet@lists.utsouthwestern.edu
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CAEBNytUc2fe1o4Z2xv5AT_JFM46+c3Ya-g=xtgmneumntkh...@mail.gmail.com
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I do see positive nuclei in the NC. That is what I am asking about. I know
I could switch methods but my question is also why if it is happening is it
not as strong all the time? Why are the cells very light one day and dark
the next? What is causing them to stain? Just curious is all.
Eva

On Wed, Jul 25, 2012 at 10:04 AM, Reynolds,Donna M
dreyn...@mdanderson.orgwrote:


 If you are running a negative control (no primary)with your ABC staining
 wouldn't you see the same nuclear labeling in the NC ? Thus alerting you to
 false staining and indicating that you should try a HRP conjugated
 secondary or use a polymer system.
 Good discussion thank Tony.
 Donna Reynolds HT(ASCP) Chief Histologist IHC Lab

 -Original Message-
  I understand the point about the biotin and I should have said that
  when using the ABC method we have taken to always using an
  avidin/biotin blocking kit. We are using biotinylated secondary
  antibodies from Vector. I have seen the same problem occur in our
  anti-mouse, anti-rabbit and anti-goat. In my last run I had stomach
  fundus as well as skin melanoma, both had pos.nuclei in the negative
  (no primary). In another run I had colon ca and breast ca, the breast
  ca had fewer pos. nuclei than the colon ca but they were still there.
  Some days the positive nuclei are stronger in a sample that was just
  weakly positive before. Just want to understand what it is and what
 effects it.
  Thank you all for your ideas.
  Eva Permaul
  Georgetown University
 
  On Mon, Jul 23, 2012 at 7:16 PM, Tony Henwood (SCHN) 
  tony.henw...@health.nsw.gov.au wrote:
 
  I should have added that this was from the workshop notes on a
  Hypotheticals Workshop I ran last year at our Australian National
 Meeting.
 
  Regards
  Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
  Laboratory Manager  Senior Scientist
  Tel: 612 9845 3306
  Fax: 612 9845 3318
  the children's hospital at westmead
  Cnr Hawkesbury Road and Hainsworth Street, Westmead Locked Bag 4001,
  Westmead NSW 2145, AUSTRALIA
 
 
  -Original Message-
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