Resultats de la cerca - Alrashed, May
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Landscape of somatic mutations in breast cancer: new opportunities for targeted therapies in Saudi Arabian patients per Barakeh, Duna H., Aljelaify, Rasha, Bashawri, Yara, Almutairi, Amal, Alqubaishi, Fatimah, Alnamnakani, Mohammed, Almubarak, Latifa, Al Naeem, Abdulrahman, Almushawah, Fatema, Alrashed, May, Abedalthagafi, Malak
Publicat 2021Text -
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Assessment of DNA damage in relation to heavy metal induced oxidative stress in females with recurrent pregnancy loss (RPL) per Alrashed, May, Tabassum, Hajera, Almuhareb, Nouf, Almutlaq, Nourah, Alamro, Waad, Alanazi, Samyah T., Alenazi, Fouza K., Alahmed, Lulwah B., Al Abudahash, Mubark M., Alenzi, Naif D.
Publicat 2021Text -
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Detection of Novel Biallelic Causative Variants in COL7A1 Gene by Whole-Exome Sequencing, Resulting in Congenital Recessive Dystrophic Epidermolysis Bullosa in Three Unrelated Fami... per Fozia, Fozia, Nazli, Rubina, Alrashed, May Mohammed, Ghneim, Hazem K., Haq, Zia Ul, Jabeen, Musarrat, Alam Khan, Sher, Ahmad, Ijaz, Bourhia, Mohammed, Aboul-Soud, Mourad A. M.
Publicat 2022Text -
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In search of triallelism in Bardet–Biedl syndrome per Abu-Safieh, Leen, Al-Anazi, Shamsa, Al-Abdi, Lama, Hashem, Mais, Alkuraya, Hisham, Alamr, Mushari, Sirelkhatim, Mugtaba O, Al-Hassnan, Zuhair, Alkuraya, Basim, Mohamed, Jawahir Y, Al-Salem, Ahmad, Alrashed, May, Faqeih, Eissa, Softah, Ameen, Al-Hashem, Amal, Wali, Sami, Rahbeeni, Zuhair, Alsayed, Moeen, Khan, Arif O, Al-Gazali, Lihadh, Taschner, Peter EM, Al-Hazzaa, Selwa, Alkuraya, Fowzan S
Publicat 2012Text -
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Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes per Abu-Safieh, Leen, Alrashed, May, Anazi, Shamsa, Alkuraya, Hisham, Khan, Arif O., Al-Owain, Mohammed, Al-Zahrani, Jawahir, Al-Abdi, Lama, Hashem, Mais, Al-Tarimi, Salwa, Sebai, Mohammed-Adeeb, Shamia, Ahmed, Ray-zack, Mohamed D., Nassan, Malik, Al-Hassnan, Zuhair N., Rahbeeni, Zuhair, Waheeb, Saad, Alkharashi, Abdullah, Abboud, Emad, Al-Hazzaa, Selwa A.F., Alkuraya, Fowzan S.
Publicat 2013Text -
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Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19 per Povysil, Gundula, Butler-Laporte, Guillaume, Shang, Ning, Weng, Chen, Khan, Atlas, Alaamery, Manal, Nakanishi, Tomoko, Zhou, Sirui, Forgetta, Vincenzo, Eveleigh, Robert, Bourgey, Mathieu, Aziz, Naveed, Jones, Steven, Knoppers, Bartha, Scherer, Stephen, Strug, Lisa, Lepage, Pierre, Ragoussis, Jiannis, Bourque, Guillaume, Alghamdi, Jahad, Aljawini, Nora, Albes, Nour, Al-Afghani, Hani M., Alghamdi, Bader, Almutair, Mansour, Mahmoud, Ebrahim Sabri, Safie, Leen Abu, Bardisy, Hadeel El, Al Harthi, Fawz S., Alshareef, Abdulraheem, Suliman, Bandar Ali, Alqahtani, Saleh, AlMalik, Abdulaziz, Alrashed, May M., Massadeh, Salam, Mooser, Vincent, Lathrop, Mark, Arabi, Yaseen, Mbarek, Hamdi, Saad, Chadi, Al-Muftah, Wadha, Badji, Radja, Al Thani, Asma, Ismail, Said I., Gharavi, Ali G., Abedalthagafi, Malak S., Richards, J Brent, Goldstein, David B., Kiryluk, Krzysztof
Publicat 2020Text -
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Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 per Povysil, Gundula, Butler-Laporte, Guillaume, Shang, Ning, Wang, Chen, Khan, Atlas, Alaamery, Manal, Nakanishi, Tomoko, Zhou, Sirui, Forgetta, Vincenzo, Eveleigh, Robert J.M., Bourgey, Mathieu, Aziz, Naveed, Jones, Steven J.M., Knoppers, Bartha, Scherer, Stephen W., Strug, Lisa J., Lepage, Pierre, Ragoussis, Jiannis, Bourque, Guillaume, Alghamdi, Jahad, Aljawini, Nora, Albes, Nour, Al-Afghani, Hani M., Alghamdi, Bader, Almutairi, Mansour S., Mahmoud, Ebrahim Sabri, Abu-Safieh, Leen, El Bardisy, Hadeel, Harthi, Fawz S. Al, Alshareef, Abdulraheem, Suliman, Bandar Ali, Alqahtani, Saleh A., Almalik, Abdulaziz, Alrashed, May M., Massadeh, Salam, Mooser, Vincent, Lathrop, Mark, Fawzy, Mohamed, Arabi, Yaseen M., Mbarek, Hamdi, Saad, Chadi, Al-Muftah, Wadha, Jung, Junghyun, Mangul, Serghei, Badji, Radja, Thani, Asma Al, Ismail, Said I., Gharavi, Ali G., Abedalthagafi, Malak S., Richards, J. Brent, Goldstein, David B., Kiryluk, Krzysztof
Publicat 2021Text