Search Results - "Faisal, Saima"

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  1. 1

    Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study by Rashid, Muhammad Usman, Muhammad, Noor, Naeemi, Humaira, Khan, Faiz Ali, Hassan, Mariam, Faisal, Saima, Gull, Sidra, Amin, Asim, Loya, Asif, Hamann, Ute

    Published in Hereditary cancer in clinical practice (11-09-2019)
    “…Pathogenic germline mutations in and ( ) account for the majority of hereditary breast and/or ovarian cancers worldwide. To refine the spectrum of mutations…”
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    Journal Article
  2. 2

    High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients by Rashid, Muhammad Usman, Muhammad, Noor, Bajwa, Seerat, Faisal, Saima, Tahseen, Muhammad, Bermejo, Justo Lorenzo, Amin, Asim, Loya, Asif, Hamann, Ute

    Published in BMC cancer (23-08-2016)
    “…Women harboring BRCA1/2 germline mutations have high lifetime risk of developing breast/ovarian cancer. The recommendation to pursue BRCA1/2 testing is based…”
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    Journal Article
  3. 3

    The Impact of Culture and Sociological and Psychological Issues on Muslim Patients With Breast Cancer in Pakistan by Banning, Maggi, Hafeez, Haroon, Faisal, Saima, Hassan, Mariam, Zafar, Ammarah

    Published in Cancer nursing (01-07-2009)
    “…Breast cancer is the most common form of cancer in Muslim women in Pakistan. The impact of the initial diagnosis, culture, religion, and psychosocial and…”
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    Journal Article
  4. 4

    Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan by Rashid, Muhammad U, Muhammad, Noor, Faisal, Saima, Amin, Asim, Hamann, Ute

    Published in BMC cancer (27-06-2013)
    “…Less than 20% of Pakistani women with early-onset or familial breast/ovarian cancer harbor germ line mutations in the high-penetrance genes BRCA1, BRCA2 and…”
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    Journal Article
  5. 5

    Patterns of cancer cell sphere formation in primary cultures of human oral tongue squamous cell carcinoma and neck nodes by Saleem, Saira, Jamshed, Arif, Faisal, Saima, Hussain, Raza, Tahseen, Muhammad, Loya, Asif, Sutton, Chris

    Published in Cancer cell international (21-12-2014)
    “…Recently a sub-population of cells with stem cell characteristics, reported to be associated with initiation, growth, spread and recurrence, has been…”
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    Journal Article
  6. 6

    Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan by Rashid, Muhammad U., Muhammad, Noor, Faisal, Saima, Amin, Asim, Hamann, Ute

    Published in Breast cancer research and treatment (01-06-2014)
    “…RAD51C plays a key role in homologous recombination-mediated DNA repair and maintenance of genomic stability. Biallelic RAD51C mutations cause Fanconi anemia,…”
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    Journal Article
  7. 7

    Constitutional CHEK2mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan by Rashid, Muhammad U, Muhammad, Noor, Faisal, Saima, Amin, Asim, Hamann, Ute

    Published in BMC cancer (27-06-2013)
    “…Background Less than 20% of Pakistani women with early-onset or familial breast/ovarian cancer harbor germ line mutations in the high-penetrance genes BRCA1,…”
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    Journal Article
  8. 8

    Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan by Rashid, Muhammad U., Gull, Sidra, Faisal, Saima, Khaliq, Saba, Asghar, Kashif, Siddiqui, Neelam, Amin, Asim, Hamann, Ute

    Published in Familial cancer (01-12-2011)
    “…Pathogenic germ line mutations in the BRCA1 and BRCA2 genes confer elevated risk of breast and ovarian cancer in females and have a link with variety of…”
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    Journal Article