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    <loc>https://weillcornellmicroscopy.org/education-program-1</loc>
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    <lastmod>2018-05-25</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-5</loc>
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    <lastmod>2018-05-25</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-4</loc>
    <changefreq>monthly</changefreq>
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    <lastmod>2018-05-02</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-3</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-02-23</lastmod>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-1-dmzla</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-01-19</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-64dxd</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-02-07</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-2-sff7e-y8rwd</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-01-18</lastmod>
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  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-2-sff7e</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-01-18</lastmod>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-2</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-01-18</lastmod>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018-1</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-02-07</lastmod>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-1/2018</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2018-01-18</lastmod>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-2</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2019-07-10</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1513795785340-B11EVQ19302XPIQZO3T1/apple-education-school-knowledge-60583.jpeg</image:loc>
      <image:title>Monthly Education Program - Didactic lectures on microscopy and image analysis</image:title>
      <image:caption>These lectures are held once a month, given mostly by Core Co-Director, Sushmita Mukherjee. Occasionally, we have guest lecturers. WHEN: Second Thursday of the month WHAT TIME: 2-3 pm WHERE: Weill Education Center, 2nd floor, C Building, 1300 York Avenue, Rooms G/H To sign up, please click this link</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1513795785340-B11EVQ19302XPIQZO3T1/apple-education-school-knowledge-60583.jpeg</image:loc>
      <image:title>Monthly Education Program - Didactic lectures on microscopy and image analysis</image:title>
      <image:caption>These lectures are held once a month, given mostly by Core Co-Director, Sushmita Mukherjee. Occasionally, we have guest lecturers. WHEN: Second Thursday of the month WHAT TIME: 2-3 pm WHERE: Weill Education Center, 2nd floor, C Building, 1300 York Avenue, Rooms G/H To sign up, please click this link</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1513796106706-YAG0NQGY6C7IC5OLFTVL/Airyscan.jpg</image:loc>
      <image:title>Monthly Education Program - Introductory lecture on use of Zeiss LSM880 confocal microscope</image:title>
      <image:caption>This class is designed to familiarize potential users with the Zeiss 880  confocal microscope and the ZEN software. Topics covered also include basic optics concepts such as wide field vs confocal imaging, resolution, resolution vs detection, the role of wavelength and/or lens choice on resolution and imaging, standard vs GaAsP (high-sensitivity) detectors. These lectures are held once a month, given mostly by Core Co-Director, Lee Cohen-Gould.  WHEN: Third Wednesday of the month WHAT TIME: 2-4 pm WHERE: A106, 1300 York Avenue To sign up, please email Lee Cohen-Gould (lcgould@med.cornell.edu)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/education-program-2-1</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2017-12-20</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1513797333559-GPUJMBQUW0SCR2BMQZZ3/one+on+one.jpg</image:loc>
      <image:title>One-on-One Consultation - One-on-one consultation and assistance</image:title>
      <image:caption>The Core Directors are available for one-on-one consultation and assistance at all levels of the microscopy enterprise, including: * experimental strategy, optimal dyes, best dishes or animal holding chambers * individual or small group training for independent image acquisition * assistance with acquisition setup for complex experiments to ensure the best possible data acquisition * assistance with image acquisition * developing image analysis strategies and training on relevant software * assisted image analysis * assisted or independent tissue processing and staining for electron microscopy and histology</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1513797333559-GPUJMBQUW0SCR2BMQZZ3/one+on+one.jpg</image:loc>
      <image:title>One-on-One Consultation - One-on-one consultation and assistance</image:title>
      <image:caption>The Core Directors are available for one-on-one consultation and assistance at all levels of the microscopy enterprise, including: * experimental strategy, optimal dyes, best dishes or animal holding chambers * individual or small group training for independent image acquisition * assistance with acquisition setup for complex experiments to ensure the best possible data acquisition * assistance with image acquisition * developing image analysis strategies and training on relevant software * assisted image analysis * assisted or independent tissue processing and staining for electron microscopy and histology</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/microscopes</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2025-04-09</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1514920334355-B6P4BLIVYPTAPC9K077I/Zeiss+AxioPlan.jpg</image:loc>
      <image:title>Microscopes - Widefield microscopy</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1514920334355-B6P4BLIVYPTAPC9K077I/Zeiss+AxioPlan.jpg</image:loc>
      <image:title>Microscopes - Widefield microscopy</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1514920333486-VV1KIYQESWH77FHFKVTI/Airyscan.jpg</image:loc>
      <image:title>Microscopes - Confocal Microscopy</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1514920334078-F6SRWJPNLP4GOSK0I8KH/MPM+only.jpg</image:loc>
      <image:title>Microscopes - Multiphoton Microscopy</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1702485033752-8RPWEF5JZ3KEWH6Q9V75/Ultramicroscope.png</image:loc>
      <image:title>Microscopes - Light Sheet Microscopy</image:title>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1514920333525-8RI682Y0GXIE7URQ479M/electron+microscope.jpg</image:loc>
      <image:title>Microscopes - Electron Microscopy</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1543336039512-K6Y4X9JLL2LXXEA5CJR7/20181119_125720.jpg</image:loc>
      <image:title>Microscopes - Automated Optical Microscopy</image:title>
      <image:caption />
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/image-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2018-01-22</lastmod>
    <image:image>
      <image:loc>https://static1.squarespace.com/static/584b2a2c37c5812f78aca714/t/5a664150c830254de2f26194/1516384694786/</image:loc>
      <image:title>Image gallery</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://static1.squarespace.com/static/584b2a2c37c5812f78aca714/5a6231954192023b5f679076/5a6231b6e2c483b6699f221a/1516384694786/</image:loc>
      <image:title>Image gallery</image:title>
      <image:caption />
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384719600-TUEJGQU3RUXB4770SPCT/COS-7_overlay.jpg</image:loc>
      <image:title>Image gallery - COS-7 cells expressing abnormal form of microtubule plus-end binding protein. MTs = red, yellow = plus-end binding protein</image:title>
      <image:caption>Credit: Katsuhiro Kita, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384858031-H1IMTO9JW5DJIQ2CU2PA/Mouse+colon+large.jpg</image:loc>
      <image:title>Image gallery - Fresh mouse colon (unfixed, unstained) imaged using multiphoton microscopy. Green and Blue: autofluorescence at short and long wavelengths; red: Second Harmonic Generation (SHG)</image:title>
      <image:caption>Credit: Manu Jain, Sushmita Mukherjee (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516385714420-SHJRRXHSZACRLBTZHH7Y/Picture9.png</image:loc>
      <image:title>Image gallery - Primary human adipocytes isolated from breast tissue were stained with lipidTox (red)</image:title>
      <image:caption>Credit: Priya Bharadwaj, Kristy Brown (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516650827918-FJ67E3T0WN4N47KB9N2D/EB1-MTs+Overlay.jpg</image:loc>
      <image:title>Image gallery - Gastric cancer cell stained with endogenous MT-end binding protein and MTs. MTs = green, red = end-binding protein</image:title>
      <image:caption>Credit: Katsuhiro Kita, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384776879-J34P7TBMCIE3DS672DOQ/Picture5.png</image:loc>
      <image:title>Image gallery - Lipoproteins (red) being digested by macrophages (green)</image:title>
      <image:caption>Credit: Inna Grosheva, Frederick Maxfield (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384782737-WDUOSSJX6KZU77C1UJTG/Picture6.png</image:loc>
      <image:title>Image gallery - Two living  cells showing fluorescent sterol (green), a fluorescent lipid (blue) and an iron-carrying protein (transferrin, red)</image:title>
      <image:caption>The yellow color indicates places where cholesterol has entered an organelle into which the transferrin has been delivered.  Credit: Mingming Hao, Frederick Maxfield (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384787005-73TJEJG7UKCC5RQ46PL6/Picture7.png</image:loc>
      <image:title>Image gallery - Lipoproteins (red) being digested by macrophages (green)</image:title>
      <image:caption>Credit: Inna Grosheva, Frederick Maxfield</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384791865-2RXNK3GICI59BGH1BNM4/Picture8.png</image:loc>
      <image:title>Image gallery - A microglial cell (green) has internalized Alzheimer’s amyloid protein (red)</image:title>
      <image:caption>Credit: Amitabha Majumdar, Frederick Maxfield (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384805044-L6WGJKCZCU3T1H7CUH5I/weird+roud+cell_overlay.jpg</image:loc>
      <image:title>Image gallery - Gastric cancer cell treated with a tool compound showed a round and flat phenotype with strange MT bundles. MTs = green, purple = DAPI</image:title>
      <image:caption>Credit: Katsuhiro Kita, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384821978-8A28ORXHLCB5G4WNJS2N/Picture2.png</image:loc>
      <image:title>Image gallery - Circulating Tumor Cells (CTCs) pre-treatment with taxane</image:title>
      <image:caption>Credit: David Worroll, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384830673-N2WI6S6NXZD6D32FMZK3/Picture3.png</image:loc>
      <image:title>Image gallery - Circulating Tumor Cells (CTCs) post-treatment with taxane</image:title>
      <image:caption>Credit: David Worroll, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/seminars</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2019-07-15</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1518124025679-VX3RF0FFZXIO4QP3QZ0U/MIA_Seminar1_01-11-18_FINAL.jpg</image:loc>
      <image:title>Seminars - Seminar on January 11, 2018</image:title>
      <image:caption>Choosing the microscope best suited to your research interest</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1518124025679-VX3RF0FFZXIO4QP3QZ0U/MIA_Seminar1_01-11-18_FINAL.jpg</image:loc>
      <image:title>Seminars - Seminar on January 11, 2018</image:title>
      <image:caption>Choosing the microscope best suited to your research interest</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1518124029960-W4395DFA8SI8PY3J8F25/MIA_Seminar2_02-08-18_FINAL.jpg</image:loc>
      <image:title>Seminars - Seminar on February 8, 2018</image:title>
      <image:caption>Comparing and contrasting confocal and multiphoton microscopy</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1521120381841-WB3KWE0LAFGY3CEE2J4E/MIA_Seminar3_03-08-18.jpg</image:loc>
      <image:title>Seminars - Seminar on March 8, 2018</image:title>
      <image:caption>Optimizing image quality in digital microscopy</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1563220991738-SFWBOS2YR6GAYYYH6H1W/Airyscan_03-17-17-1.png</image:loc>
      <image:title>Seminars - Seminar on March 17, 2017</image:title>
      <image:caption>Zeiss Airyscan Microscopy</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/confocal-microscopy</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2024-01-03</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1580935264960-LETKBD5XNKQVSP93QKI8/Leica+SP8.jpg</image:loc>
      <image:title>Confocal Microscopy</image:title>
      <image:caption>Leica SP8 with DIVE optics, combined confocal and multiphoton microscope</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/d4ffc437-4bdc-4c31-8278-3ac4bfec46ff/Leica-Stellaris8-scaled.jpg</image:loc>
      <image:title>Confocal Microscopy - Make it stand out</image:title>
      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1580935632425-3WKN7M6V5LCOFCHC1CL3/High+content.jpg</image:loc>
      <image:title>Confocal Microscopy</image:title>
      <image:caption>ImageXpress Micro Confocal (spinning disk) automated imager</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1580935200038-PW46D0VATXP8WQP8ILPG/Airyscan.jpg</image:loc>
      <image:title>Confocal Microscopy</image:title>
      <image:caption>Zeiss LSM880 with Airyscan and environmental chamber for live cell imaging</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/db114e46-5be7-4289-bebb-7361efbe0a72/lsm880.jpg</image:loc>
      <image:title>Confocal Microscopy - Make it stand out</image:title>
      <image:caption>Zeiss LSM880 confocal microscope</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1481334908897-9CS8YC9Q0ULJWVXZSI8Y/Airyscan.jpg</image:loc>
      <image:title>Confocal Microscopy</image:title>
    </image:image>
  </url>
  <url>
    <loc>https://weillcornellmicroscopy.org/overview</loc>
    <changefreq>daily</changefreq>
    <priority>1.0</priority>
    <lastmod>2025-04-09</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384719600-TUEJGQU3RUXB4770SPCT/COS-7_overlay.jpg</image:loc>
      <image:title>Overview - COS-7 cells expressing abnormal form of microtubule plus-end binding protein. MTs = red, yellow = plus-end binding protein</image:title>
      <image:caption>Credit: Katsuhiro Kita, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384858031-H1IMTO9JW5DJIQ2CU2PA/Mouse+colon+large.jpg</image:loc>
      <image:title>Overview - Fresh mouse colon (unfixed, unstained) imaged using multiphoton microscopy. Green and Blue: autofluorescence at short and long wavelengths; red: Second Harmonic Generation (SHG)</image:title>
      <image:caption>Credit: Manu Jain, Sushmita Mukherjee (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516385714420-SHJRRXHSZACRLBTZHH7Y/Picture9.png</image:loc>
      <image:title>Overview - Primary human adipocytes isolated from breast tissue were stained with lipidTox (red)</image:title>
      <image:caption>Credit: Priya Bharadwaj, Kristy Brown (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516650827918-FJ67E3T0WN4N47KB9N2D/EB1-MTs+Overlay.jpg</image:loc>
      <image:title>Overview - Gastric cancer cell stained with endogenous MT-end binding protein and MTs. MTs = green, red = end-binding protein</image:title>
      <image:caption>Credit: Katsuhiro Kita, Paraskevi Giannakakou (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384776879-J34P7TBMCIE3DS672DOQ/Picture5.png</image:loc>
      <image:title>Overview - Lipoproteins (red) being digested by macrophages (green)</image:title>
      <image:caption>Credit: Inna Grosheva, Frederick Maxfield (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384782737-WDUOSSJX6KZU77C1UJTG/Picture6.png</image:loc>
      <image:title>Overview - Two living  cells showing fluorescent sterol (green), a fluorescent lipid (blue) and an iron-carrying protein (transferrin, red)</image:title>
      <image:caption>The yellow color indicates places where cholesterol has entered an organelle into which the transferrin has been delivered.  Credit: Mingming Hao, Frederick Maxfield (WCM)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/584b2a2c37c5812f78aca714/1516384787005-73TJEJG7UKCC5RQ46PL6/Picture7.png</image:loc>
      <image:title>Overview - Lipoproteins (red) being digested by macrophages (green)</image:title>
      <image:caption>Credit: Inna Grosheva, Frederick Maxfield</image:caption>
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