Search Results - Rosenberg, Allana

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer

    Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer by Webster, Andrew L. H., Sanders, Mathijs A., Patel, Krupa, Dietrich, Ralf, Noonan, Raymond J., Lach, Francis P., White, Ryan R., Goldfarb, Audrey, Hadi, Kevin, Edwards, Matthew M., Donovan, Frank X., Hoogenboezem, Remco M., Jung, Moonjung, Sridhar, Sunandini, Wiley, Tom F., Fedrigo, Olivier, Tian, Huasong, Rosiene, Joel, Heineman, Thomas, Kennedy, Jennifer A., Bean, Lorenzo, Rosti, Rasim O., Tryon, Rebecca, Gonzalez, Ashlyn-Maree, Rosenberg, Allana, Luo, Ji-Dung, Carroll, Thomas S., Shroff, Sanjana, Beaumont, Michael, Velleuer, Eunike, Rastatter, Jeff C., Wells, Susanne I., Surrallés, Jordi, Bagby, Grover, MacMillan, Margaret L., Wagner, John E., Cancio, Maria, Boulad, Farid, Scognamiglio, Theresa, Vaughan, Roger, Beaumont, Kristin G., Koren, Amnon, Imielinski, Marcin, Chandrasekharappa, Settara C., Auerbach, Arleen D., Singh, Bhuvanesh, Kutler, David I., Campbell, Peter J., Smogorzewska, Agata

    Published in Nature (London)
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia

    FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia by Ramanagoudr-Bhojappa, Ramanagouda, Tryon, Rebecca, Lach, Francis P., Donovan, Frank X., Maxwell, Rochelle, Rosenberg, Allana, MacMillan, Margaret L., Wagner, John E., Auerbach, Arleen D., Smogorzewska, Agata, Chandrasekharappa, Settara C.

    Published in Blood advances
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  3. 3
    Abstract 6196: Fanconi anemia pathway deficiency drives copy number variation in squamous cell carcinoma

    Abstract 6196: Fanconi anemia pathway deficiency drives copy number variation in squamous cell carcinoma by Webster, Andrew L., Sanders, Mathijs A., Patel, Krupa, Dietrich, Ralf, Noonan, Raymond J., Lach, Francis P., White, Ryan R., Goldfarb, Audrey M., Hadi, Kevin, Edwards, Matthew M., Donovan, Frank X., Jung, Moonjung, Sridhar, Sunandini, Fedrigo, Olivier, Tian, Huasong, Rosiene, Joel, Heineman, Thomas, Kennedy, Jennifer, Bean, Lorenzo, Rosti, Rasim O., Tryon, Rebecca, Gonzalez, Ashlyn-Maree, Rosenberg, Allana, Luo, Ji-Dung, Carrol, Thomas, Velleuer, Eunike, Rastatter, Jeff C., Wells, Susanne I., Surrallés, Jordi, Bagby, Grover, MacMillan, Margaret L., Wagner, John E., Cancio, Maria, Boulad, Farid, Scognamiglio, Theresa, Vaughan, Roger, Koren, Amnon, Imielinski, Marcin, Chandrasekharappa, Settara, Auerbach, Arleen D., Singh, Bhuvanesh, Kutler, David, Campbell, Peter J., Smogorzewska, Agata

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: