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24 result(s) for 'author#Mamdooh Gari' within BMC

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  1. O1 Regulation of genes by telomere length over long distances

    Authors: Jerry W. Shay, Noriko Homma, Ruyun Zhou, Muhammad Imran Naseer, Adeel G. Chaudhary, Mohammed Al-Qahtani, Nobutaka Hirokawa, Maryam Goudarzi, Albert J. Fornace Jr., Saleh Baeesa, Deema Hussain, Mohammed Bangash, Fahad Alghamdi, Hans-Juergen Schulten, Angel Carracedo, Ishaq Khan…
    Citation: BMC Genomics 2016 17(Suppl 6):487

    This article is part of a Supplement: Volume 17 Supplement 6

  2. Osteoarthritis (OA) is a progressive joint disease characterized by gradual degradation of extracellular matrix (ECM) components in the cartilage and bone. The ECM of cartilage is a highly specified structure ...

    Authors: Mamdooh Abdullah Gari, Mohammed AlKaff, Haneen S. Alsehli, Ashraf Dallol, Abdullah Gari, Muhammad Abu-Elmagd, Roaa Kadam, Mohammed F. Abuzinadah, Mazin Gari, Adel M. Abuzenadah, Kalamegam Gauthaman, Heba Alkhatabi and Mohammed M. Abbas
    Citation: BMC Medical Genetics 2016 17(Suppl 1):68

    This article is part of a Supplement: Volume 17 Supplement 1

  3. Benign neutropenia often presents in certain populations without any genotype nor phenotype. Middle East countries are among the regions where endemic cases of chronic benign neutropenia are reported in the ge...

    Authors: Mamdooh Gari, Mohammed Dakhakhni, Abdullah Gari, Erada Alshihri, Rowan Al-Jahdali, Kothandaraman Narasimhan, Shen Liang, Fatin Al-Sayes, Gauthaman Kalamegam, Adeel Chaudhary, Adel Abuzenadah and Mohammed Al-Qahtani
    Citation: BMC Proceedings 2015 9(Suppl 2):S1

    This article is part of a Supplement: Volume 9 Supplement 2

  4. The molecular etiology of thyroid carcinoma (TC) and other thyroid diseases which may present malignant precursor lesions is not fully explored yet. The purpose of this study was to estimate frequency, type an...

    Authors: Hans-Juergen Schulten, Sherine Salama, Zuhoor Al-Mansouri, Reem Alotibi, Khalid Al-Ghamdi, Osman Abdel Al-Hamour, Hassan Sayadi, Hosam Al-Aradati, Adel Al-Johari, Etimad Huwait, Mamdooh Gari, Mohammed Hussain Al-Qahtani and Jaudah Al-Maghrabi
    Citation: Hereditary Cancer in Clinical Practice 2012 10:10
  5. Authors: Adnan Merdad, Sajjad Karim, Hans-Juergen Schulten, Ashraf Dallol, Abdelbaset S Buhmeida, Fatima Al-Thubaity, Manar M Ata, Mamdooh A Gari, Adeel GA Chaudhary, Adel M Abuzenadah and Mohammed H Al-Qahtani
    Citation: BMC Genomics 2014 15(Suppl 2):P55

    This article is part of a Supplement: Volume 15 Supplement 2

  6. Authors: Sherin Bakhashab, Sahira Lari, Farid Ahmed, Hans-Juergen Schulten, Manikandan Jayapal, Sajjad Karim, Ayat Bashir, Fahad Ahmed, Abdulrahman Al-Malki, Hasan S Jamal, Mamdooh Gari, Mohammed H. Alqahtani, Ioakim Spyridopoulos and Jolanta U Weaver
    Citation: BMC Genomics 2014 15(Suppl 2):P23

    This article is part of a Supplement: Volume 15 Supplement 2

  7. Authors: Alaa Al-Ahmadi, Reem Alotibi, Maha Al-Quaiti, Fai Ashgan, Kothandaraman Narasimhan, Etimad Huwait, Mamdooh Gari, Mohammed Hussein Al-Qahtani, Jaudah Al-Maghrabi and Hans-Juergen Schulten
    Citation: BMC Genomics 2014 15(Suppl 2):P62

    This article is part of a Supplement: Volume 15 Supplement 2

  8. Authors: Sahar Hakamy, Basmat Abdallah, Abdelbaset Buhmeida, Ashraf Dallol, Adnan Merdad, Jaudah Al-Maghrabi, Muhammad Abu-Elmagd, Mamdooh Gari, Adeel Chaudhary, Adel Abuzenadah, Taoufik Nedjadi, Eramah Ermiah, Fatima Thubaity and Mohammed Al-Qahtani
    Citation: BMC Genomics 2014 15(Suppl 2):P35

    This article is part of a Supplement: Volume 15 Supplement 2

  9. Authors: Reham Al Nono, Gauthaman Kalamegam, Haneen Alsehli, Farid Ahmed, Mohammed Alkaff, Mohammed Abbas, Wael Kafienah, Faten Al Sayes, Adeel Chaudhary, Adel Abuzenadah, Mohammed Al Qahtani and Mamdooh Gari
    Citation: BMC Genomics 2014 15(Suppl 2):P37

    This article is part of a Supplement: Volume 15 Supplement 2

  10. Authors: Shireen Hussein, Adnan Merdad, Jaudah Al-Maghrabi, Mamdooh A. Gari, Fatma Al-Thubaiti, Ibtessam R. Hussein, Adeel G. Chaudhary, Adel M. Abuzenadah, Hanaa Tashkandi, Shadi Al-Khayyat, Taha Kumosani, Mohammed H. Al-Qahtani and Ashraf Dallol
    Citation: BMC Genomics 2014 15(Suppl 2):P20

    This article is part of a Supplement: Volume 15 Supplement 2

  11. Glucose-6-phosphate dehydrogenase (G6PD, EC 1.1.1.49) deficiency is caused by one or more mutations in the G6PD gene on chromosome X. An association between enzyme levels and gene haplotypes remains to be establi...

    Authors: Ashraf Dallol, Huda Banni, Mamdooh A Gari, Mohammed H Al-Qahtani, Adel M Abuzenadeh, Fatin Al-Sayes, Adeel G Chaudhary, Jeffrey Bidwell and Wael Kafienah
    Citation: Journal of Translational Medicine 2012 10:199
  12. Hearing Impairment (HI) can have genetic or environmental causes and in some cases, an interplay of both. Genetic causes are difficult to determine as mutations in more than 90 genes have been shown recently t...

    Authors: Ashraf Dallol, Kamal Daghistani, Aisha Elaimi, Wissam A. Al-Wazani, Afaf Bamanie, Malek Safiah, Samira Sagaty, Layla Taha, Rawabi Zahed, Osama Bajouh, Adeel Gulzar Chaudhary, Mamdooh Abdullah Gari, Rola Turki, Mohammed Hussein Al-Qahtani and Adel Mohammed Abuzenadah
    Citation: BMC Medical Genetics 2016 17(Suppl 1):67

    This article is part of a Supplement: Volume 17 Supplement 1

  13. The contribution of genetic factors to the development of breast cancer in the admixed and consanguineous population of the western region of Saudi Arabia is thought to be significant as the disease is early o...

    Authors: Adnan Merdad, Mamdooh A Gari, Shireen Hussein, Shadi Al-Khayat, Hana Tashkandi, Jaudah Al-Maghrabi, Fatma Al-Thubaiti, Ibtessam R Hussein, Taha Koumosani, Nehad Shaer, Adeel G Chaudhary, Adel M Abuzenadah, Mohammed H Al-Qahtani and Ashraf Dallol
    Citation: BMC Genomics 2015 16(Suppl 1):S3

    This article is part of a Supplement: Volume 16 Supplement 1

  14. Acute myeloid leukemia (AML) is a clonal disorder of the blood forming cells characterized by accumulation of immature blast cells in the bone marrow and peripheral blood. Being a heterogeneous disease, AML ha...

    Authors: Asad Muhammad Ilyas, Sultan Ahmad, Muhammad Faheem, Muhammad Imran Naseer, Taha A Kumosani, Muhammad Hussain Al-Qahtani, Mamdooh Gari and Farid Ahmed
    Citation: BMC Genomics 2015 16(Suppl 1):S5

    This article is part of a Supplement: Volume 16 Supplement 1