Ngā hua rapu - Raj Ramesar

Whakamahine hua
  1. 1
    A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis

    A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis mā Lindsay Gleghorn, Raj Ramesar, Peter Beighton, Gillian A. Wallis

    I whakaputaina 2005
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    Immunogenomic Biomarkers for Early Cancer Detection in Lynch Syndrome

    Immunogenomic Biomarkers for Early Cancer Detection in Lynch Syndrome mā Ramadhani Chambuso, Mbali Mthembu, Evelyn Kaambo, Barbara Robertson, Raj Ramesar

    I whakaputaina 2022
    Whiwhi kuputuhi katoa
    Pré-impressão
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  3. 3
    Psychosocial Burden of Sickle Cell Disease on Parents with an Affected Child in Cameroon

    Psychosocial Burden of Sickle Cell Disease on Parents with an Affected Child in Cameroon mā Ambroise Wonkam, Caryl Zameyo, Dora Mbanya, Jeanne Ngogang, Raj Ramesar, Fru Angwafo

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    PXR and CAR single nucleotide polymorphisms influence plasma efavirenz levels in South African HIV/AIDS patients

    PXR and CAR single nucleotide polymorphisms influence plasma efavirenz levels in South African HIV/AIDS patients mā Marelize Swart, Heather Whitehorn, Yuan Ren, Peter J. Smith, Raj Ramesar, Collet Dandara

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    Neuropsychological status of bipolar I disorder: impact of psychosis

    Neuropsychological status of bipolar I disorder: impact of psychosis mā Jonathan Savitz, Lize van der Merwe, Dan J. Stein, Mark Solms, Raj Ramesar

    I whakaputaina 2009
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    A Genomic Portrait of Haplotype Diversity and Signatures of Selection in Indigenous Southern African Populations

    A Genomic Portrait of Haplotype Diversity and Signatures of Selection in Indigenous Southern African Populations mā Emile R. Chimusa, Ayton Meintjies, Milaine Tchanga, Nicola Mulder, Cathal Seoighe, Himla Soodyall, Raj Ramesar

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    Identification of a mutation in the ubiquitin-fold modifier 1-specific peptidase 2 gene, UFSP2, in an extended South African family with Beukes hip dysplasia

    Identification of a mutation in the ubiquitin-fold modifier 1-specific peptidase 2 gene, UFSP2, in an extended South African family with Beukes hip dysplasia mā Christopher M. Watson, Laura A. Crinnion, Lindsay Gleghorn, William G. Newman, Raj Ramesar, Peter Beighton, Gillian A. Wallis

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival

    The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improv... mā Maryam Bibi Rumaney, Valentina Josiane Ngo Bitoungui, Anna Alvera Vorster, Raj Ramesar, André Pascal Kengne, Jeanne Ngogang, Ambroise Wonkam

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Association of Variants at BCL11A and HBS1L-MYB with Hemoglobin F and Hospitalization Rates among Sickle Cell Patients in Cameroon

    Association of Variants at BCL11A and HBS1L-MYB with Hemoglobin F and Hospitalization Rates among Sickle Cell Patients in Cameroon mā Ambroise Wonkam, Valentina Josiane Ngo Bitoungui, Anna Alvera Vorster, Raj Ramesar, Stephen S. Rich, Bamidele O. Tayo, Guillaume Lettre, Jeanne Ngogang

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    Determining Ancestry Proportions in Complex Admixture Scenarios in South Africa Using a Novel Proxy Ancestry Selection Method

    Determining Ancestry Proportions in Complex Admixture Scenarios in South Africa Using a Novel Proxy Ancestry Selection Method mā Emile R. Chimusa, Michelle Daya, Marlo Möller, Raj Ramesar, Brenna M. Henn, Paul D. van Helden, Nicola Mulder, Eileen G. Hoal

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats

    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats mā Maria Teresa Bassi, Raj Ramesar, Barbara Caciotti, Ingrid Winship, Alessandro De Grandi, Mirko Riboni, Philip L. Townes, Peter Beighton, Andrea Ballabio, Giuseppe Borsani

    I whakaputaina 1999
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Age, absolute CD4 count, and CD4 percentage in relation to HPV infection and the stage of cervical disease in HIV-1-positive women

    Age, absolute CD4 count, and CD4 percentage in relation to HPV infection and the stage of cervical disease in HIV-1-positive women mā Ramadhani Chambuso, Raj Ramesar, Evelyn Kaambo, Alltalents T. Murahwa, Mohammed O. E. Abdallah, Michelle De Sousa, Lynette Denny, Anna‐Lise Williamson, Clive M. Gray

    I whakaputaina 2020
    Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa

    Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa mā George Rebello, Raj Ramesar, Alvera Vorster, Lisa Roberts, Liezle Ehrenreich, Ekow Oppon, Dumisani Gama, Soraya Bardien, Jacquie Greenberg, Giuseppe Bonapace, Abdül Waheed, Gul N. Shah, William S. Sly

    I whakaputaina 2004
    Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in<i>ABCC6</i>

    Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in<i>ABCC6</i> mā Sara Miksch, Amanda L. Lumsden, Ulf P. Guenther, Dorothee Foernzler, Stéphanie Christen-Zäch, Carol Daugherty, Raj Ramesar, Mark Lebwohl, Daniel Hohl, Kenneth H. Neldner, Klaus Lindpaintner, Robert I. Richards, Berthold Struk

    I whakaputaina 2005
    Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    Genomic Structure and Identification of Novel Mutations in Usherin, the Gene Responsible for Usher Syndrome Type IIa

    Genomic Structure and Identification of Novel Mutations in Usherin, the Gene Responsible for Usher Syndrome Type IIa mā Michael D. Weston, James D. Eudy, Shigetoshi Fujita, S.-F. Yao, Shin‐ichi Usami, Cor W. R. J. Cremers, J. Greenburg, Raj Ramesar, Alessandro Martini, C. Möller, Richard J. Smith, János Sümegi, William J. Kimberling

    I whakaputaina 2000
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans

    Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans mā Ananyo Choudhury, Michèle Ramsay, Scott Hazelhurst, Shaun Aron, Soraya Bardien, Gerrit Botha, Emile R. Chimusa, Alan Christoffels, Junaid Gamieldien, Mahjoubeh J. Sefid-Dashti, Fourie Joubert, Ayton Meintjes, Nicola Mulder, Raj Ramesar, D. Jasper G. Rees, Kathrine Scholtz, Dhriti Sengupta, Himla Soodyall, Philip A. Venter, Louise Warnich, Michael S. Pepper

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

    Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK mā Ernst Reichenberger, Valdenize Tiziani, Shôji Watanabe, Lucy Park, Yasuyoshi Ueki, Carla Santanna, Scott T. Baur, Rita Shiang, Dorothy K. Grange, Peter Beighton, Jessica C. Gardner, Herman A. Hamersma, S. L. Sellars, Raj Ramesar, Andrew C. Lidral, Annmarie Sommer, Cassio Menezes Raposo do Amaral, Robert J. Gorlin, John B. Mulliken, Bjørn R. Olsen

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up

    Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up mā John C. Mathers, Faye Elliott, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Fiona E. McRonald, Lucio Bertario, D. Gareth Evans, Anne‐Marie Gerdes, Judy Ho, Annika Lindblom, Patrick J. Morrison, Jem Rashbass, Raj Ramesar, Toni T. Seppälä, Huw Thomas, Harsh Sheth, Kirsi Pylvänäinen, Lynn Reed, Gillian M. Borthwick, D. Timothy Bishop, John Burn

    I whakaputaina 2022
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma

    Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma mā Laurence Pierrache, Adva Kimchi, Rinki Ratnapriya, Lisa Roberts, Galuh Astuti, Alexey Obolensky, Avigail Beryozkin, Martha J. H. Tjon-Fo-Sang, J. Schuil, Caroline C. W. Klaver, Ernie M.H.F. Bongers, Lonneke Haer‐Wigman, Nicoline Schalij, Martijn H. Breuning, Gratia M. Fischer, Eyal Banin, Raj Ramesar, Anand Swaroop, L. Ingeborgh van den Born, Dror Sharon, Frans P.M. Cremers

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

    Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study mā Mohammad Movahedi, D. Timothy Bishop, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Sylviane Olschwang, Diana Eccles, D. Gareth Evans, Eamonn R. Maher, Lucio Bertario, Marie-Luise Bisgaard, Malcolm G. Dunlop, Judy W.C. Ho, Shirley V. Hodgson, Annika Lindblom, Jan Lubiński, Patrick J. Morrison, Victoria Murday, Raj Ramesar, Lucy Side, Rodney J. Scott, Huw Thomas, Hans F. A. Vasen, John Burn, John C. Mathers

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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