Resultats de la cerca - Brian F. Meyer

Refinar resultats
  1. 1
    Localization of the Gene for a Novel Autosomal Recessive Neurodegenerative Huntington-Like Disorder to 4p15.3

    Localization of the Gene for a Novel Autosomal Recessive Neurodegenerative Huntington-Like Disorder to 4p15.3 per Marios Kambouris, Saeed Bohlega, Abdulrahman AlTahan, Brian F. Meyer

    Publicat 2000
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  2. 2
    The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population

    The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population per Faiqa Imtiaz, Erkki Savilahti, Annikki Sarnesto, Daniah Trabzuni, Khalid Al-Kahtani, Ingvar Kagevi, M. S. Rashed, Brian F. Meyer, Irma Järvelä

    Publicat 2007
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  3. 3
    Concomitant<i>RAS</i>,<i>RET/PTC</i>, or<i>BRAF</i>Mutations in Advanced Stage of Papillary Thyroid Carcinoma

    Concomitant<i>RAS</i>,<i>RET/PTC</i>, or<i>BRAF</i>Mutations in Advanced Stage of Papillary Thyroid Carcinoma per Minjing Zou, Essa Y. Baitei, Ali S. Alzahrani, Faisal S. BinHumaid, Dania Alkhafaji, Roua A. Al‐Rijjal, Brian F. Meyer, Yufei Shi

    Publicat 2014
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  4. 4
    Perceptions of Colorectal Cancer Screening in Urban African American Clinic Patients: Differences by Gender and Screening Status

    Perceptions of Colorectal Cancer Screening in Urban African American Clinic Patients: Differences by Gender and Screening Status per Sarah Bauerle Bass, Thomas F. Gordon, Sheryl Burt Ruzek, Caitlin Wolak, Stephanie Ward, Anuradha Paranjape, Karen Lin, Brian F. Meyer, Dominique G. Ruggieri

    Publicat 2010
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  5. 5
    RAGE-mediated neutrophil dysfunction is evoked by advanced glycation end products (AGEs)

    RAGE-mediated neutrophil dysfunction is evoked by advanced glycation end products (AGEs) per Kate S. Collison, Ranjit S. Parhar, Soad Saleh, Brian F. Meyer, Aaron Kwaasi, Muhammad M. Hammami, Ann Marie Schmidt, David M. Stern, Futwan Al‐Mohanna

    Publicat 2002
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  6. 6
    High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots

    High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried... per Hamoud Al‐Mousa, Ghadah Aldakheel, Amal Jabr, Fahd El‐Badaoui, Mohamed Abouelhoda, Mansoor Ali Baig, Dorota Monies, Brian F. Meyer, Abbas Hawwari, Majed Dasouki

    Publicat 2018
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  7. 7
    Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population

    Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population per Osama Alsmadi, Khalid Al‐Rubeaan, Gamal Mohamed, Fadi Alkayal, Haya Al‐Saud, Nouran Abu Al‐Saud, Nasser M. Al‐Daghri, Shahinaz Mohammad, Brian F. Meyer

    Publicat 2008
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  8. 8
    Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A

    Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A per Korcan Demir, Walaa E. Kattan, Minjing Zou, Erdem Durmaz, Huda A. BinEssa, Özlem Nalbantoğlu, Roua A. Al‐Rijjal, Brian F. Meyer, Behzat Özkan, Yufei Shi

    Publicat 2015
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  9. 9
    Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

    Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature per José Morales, Latifa Al-Sharif, Dania S. Khalil, Jameela Shinwari, Prashant Bavi, Rahima A. Al-Mahrouqi, Ali A. Al‐Rajhi, Fowzan S. Alkuraya, Brian F. Meyer, Nada Al Tassan

    Publicat 2009
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  10. 10
    A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families

    A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families per Mohamed H. Al‐Hamed, Essam Al‐Sabban, Hamad Al‐Mojalli, Naffaa Al-Harbi, Eissa Faqeih, Hammad Al Shaya, Khalid Alhasan, Safaa Al-Hissi, Mohamed Rajab, Noel Edwards, Abbas Al-Abbad, Ibrahim A. Al-Hassoun, John A. Sayer, Brian F. Meyer

    Publicat 2013
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  11. 11
    TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer

    TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer per Minjing Zou, Essa Y. Baitei, Roua A. Al‐Rijjal, Ranjit S. Parhar, Futwan Al‐Mohanna, Shioko Kimura, Catrin Pritchard, Huda A. BinEssa, Ali S. Alzahrani, Huda H. Al‐Khalaf, Abbas Hawwari, M Akhtar, Abdullah M. Assiri, Brian F. Meyer, Yufei Shi

    Publicat 2015
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  12. 12
    Prioritizing Genetic Testing in Patients With Kallmann Syndrome Using Clinical Phenotypes

    Prioritizing Genetic Testing in Patients With Kallmann Syndrome Using Clinical Phenotypes per Flávia A. Costa‐Barbosa, Ravikumar Balasubramanian, Kimberly W. Keefe, Natalie D. Shaw, Nada Al Tassan, Lacey Plummer, Andrew Dwyer, Cassandra Buck, Jin‐Ho Choi, Stephanie B. Seminara, Richard Quinton, Dorota Monies, Brian F. Meyer, Janet E. Hall, Nelly Pitteloud, William F. Crowley

    Publicat 2013
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  13. 13
    Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis

    Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis per Minjing Zou, Ali S. Alzahrani, Ali Al‐Odaib, Mohammad A. Alqahtani, Omer Babiker, Roua A. Al‐Rijjal, Huda A. BinEssa, Walaa E. Kattan, Anwar F Al-Enezi, Ali Al Qarni, Manar S. A. Al-Faham, Essa Y. Baitei, Afaf Alsagheir, Brian F. Meyer, Yufei Shi

    Publicat 2018
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  14. 14
    Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

    Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome per Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Çolak, Hanif Khalak, Andy Baltus, Borut Peterlin, Sumita Danda, Kailash P. Bhatia, Susanne A. Schneider, Nadia Sakati, Christopher A. Walsh, Futwan Al‐Mohanna, Brian F. Meyer, Fowzan S. Alkuraya

    Publicat 2008
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  15. 15
    Functionally compromised <i>CHD7</i> alleles in patients with isolated GnRH deficiency

    Functionally compromised <i>CHD7</i> alleles in patients with isolated GnRH deficiency per Ravikumar Balasubramanian, Jin‐Ho Choi, Ludmila Francescatto, Jason R. Willer, Edward R. Horton, Eleni P. Asimacopoulos, Konstantina M. Stanković, Lacey Plummer, Cassandra Buck, Richard Quinton, Todd D. Nebesio, Verónica Mericq, Paulina M. Merino, Brian F. Meyer, Dorota Monies, James F. Gusella, Nada Al Tassan, Nicholas Katsanis, William F. Crowley

    Publicat 2014
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  16. 16
    Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture

    Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture per Nabil Enattah, Tine G.K. Jensen, Mette Ødegaard Nielsen, Rikke Lewinski, Mikko Kuokkanen, Heli Rasinperä, Hatem El‐Shanti, Jeong Kee Seo, Michael Alifrangis, Insaf F. Khalil, Abdrazak Natah, Ahmed Ali, Sirajedin Natah, David Comas, S. Qasim Mehdi, Leif Groop, Else Marie Vestergaard, Faiqa Imtiaz, Mohamed S. Rashed, Brian F. Meyer, Jesper T. Troelsen, Leena Peltonen

    Publicat 2008
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  17. 17
    Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain development

    Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain development per Michael S. Nahorski, Sateesh Maddirevula, Ryosuke Ishimura, Saud Alsahli, Angela F. Brady, Anaïs Begemann, Tsunehiro Mizushima, Francisco J. Guzmán‐Vega, Miki Obata, Yoshinobu Ichimura, Hessa S. Alsaif, Shams Anazi, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Dorota Monies, Mohamed Abouelhoda, Brian F. Meyer, Majid Alfadhel, Wafa Eyaid, Markus Zweier, Katharina Steindl, Anita Rauch, Stefan T. Arold, C. Geoffrey Woods, Masaaki Komatsu, Fowzan S. Alkuraya

    Publicat 2018
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  18. 18
    METTL23, a transcriptional partner of GABPA, is essential for human cognition

    METTL23, a transcriptional partner of GABPA, is essential for human cognition per Rachel E. Reiff, Bassam R. Ali, Byron Baron, Timothy W. Yu, Salma Ben‐Salem, Michael E. Coulter, Christian Schubert, R. Sean Hill, Nadia Akawi, Banan Al‐Younes, Namik Kaya, Gilad D. Evrony, Muna Al‐Saffar, Jillian M. Felie, Jennifer N. Partlow, Christine Sunu, Pierre Schembri-Wismayer, Fowzan S. Alkuraya, Brian F. Meyer, Christopher A. Walsh, Lihadh Al‐Gazali, Ganeshwaran H. Mochida

    Publicat 2014
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  19. 19
    A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

    A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer per Nada Al Tassan, Nicola Whiffin, Fay J. Hosking, Claire Palles, Susan M. Farrington, Sara E. Dobbins, Rebecca Harris, Maggie Gorman, Albert Tenesa, Brian F. Meyer, Salma M. Wakil, Ben Kinnersley, Harry Campbell, Lynn Martin, Christopher G. Smith, Shelley Idziaszczyk, Ella Barclay, Tim Maughan, Richard Kaplan, Rachel Kerr, David Kerr, Daniel D. Buchanan, Aung Ko Win, John L. Hopper, Mark A. Jenkins, Noralane M. Lindor, Polly A. Newcomb, Steve Gallinger, David V. Conti, Fredrick R. Schumacher, Graham Casey, Malcolm G. Dunlop, Ian Tomlinson, Jeremy P. Cheadle, Richard S. Houlston

    Publicat 2015
    Obtenir text complet Obtenir text complet
    Errata/Corrigenda
    Afegir a favorits
    Guardat en:
  20. 20
    Autozygome and high throughput confirmation of disease genes candidacy

    Autozygome and high throughput confirmation of disease genes candidacy per Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al‐Owain, Mohammad A. Al Muhaizea, Husam Kayyali, Amal Alhashem, Zuhair Rahbeeni, Maha Alotaibi, Hamad Alzaidan, Ameera Balobaid, Heba Y. El Khashab, Dalal Bubshait, Maha Faden, Suad Al Yamani, Omar Dabbagh, Mariam Almureikhi, Abdulla Al Jasser, Hessa S. Alsaif, Iram Alluhaydan, Mohammed Zain Seidahmed, Bashair Alabbasi, Ibrahim Al‐Mogarri, Wesam Kurdi, Hana Akleh, Alya Qari, Saeed M. Al Tala, Suzan Alhomaidi, Amal Y. Kentab, Mustafa A. Salih, Aziza Chedrawi, Seham Alameer, Brahim Tabarki, Hanan E. Shamseldin, Nisha Patel, Niema Ibrahim, Firdous Abdulwahab, Menasria Samira, Ewa Goljan, Mohamed Abouelhoda, Brian F. Meyer, Mais Hashem, Ranad Shaheen, Saad AlShahwan, Majid Alfadhel, Tawfeg Ben‐Omran, Mohammad M. Al‐Qattan, Dorota Monies, Fowzan S. Alkuraya

    Publicat 2018
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:

Eines de cerca: