Hasil Pencarian - Anneke I. den Hollander

Perbaiki Hasil
  1. 1
    Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.

    Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma. oleh Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Aftab Iqbal, Muhammad Imran Khan, Anneke I den Hollander

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Genetics of Unilateral and Bilateral Age-Related Macular Degeneration Severity Stages.

    Genetics of Unilateral and Bilateral Age-Related Macular Degeneration Severity Stages. oleh Tina Schick, Lebriz Altay, Eva Viehweger, Carel B Hoyng, Anneke I den Hollander, Moritz Felsch, Sascha Fauser

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE

    Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE oleh Florian Peters, Lynn J. A. Ebner, David Atac, Jordi Maggi, Wolfgang Berger, Anneke I. den Hollander, Christian Grimm

    Diterbitkan 2022-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Metabolomics and Age-Related Macular Degeneration

    Metabolomics and Age-Related Macular Degeneration oleh Connor N. Brown, Brian D. Green, Richard B. Thompson, Anneke I. den Hollander, Imre Lengyel, on behalf of the EYE-RISK consortium

    Diterbitkan 2018-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290

    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290 oleh Rob WJ Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, Jeannette Bennicelli, Jean Bennett, Frans PM Cremers

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

    A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. oleh Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Cristina Villanueva-Mendoza, Vianney Cortés-González, Muhammad Imran Khan, Anneke I den Hollander

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium

    A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium oleh Eszter Emri, Elod Kortvely, Sascha Dammeier, Franziska Klose, David Simpson, EYE-RISK Consortium, Anneke I. den Hollander, Marius Ueffing, Imre Lengyel

    Diterbitkan 2020-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotype.

    Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotype. oleh Qin Liu, Rob W J Collin, Frans P M Cremers, Anneke I den Hollander, L Ingeborgh van den Born, Eric A Pierce

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma.

    Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma. oleh Shazia Micheal, Humaira Ayub, Farrah Islam, Sorath Noorani Siddiqui, Wajid Ali Khan, Farah Akhtar, Raheel Qamar, Muhammad Imran Khan, Anneke I den Hollander

    Diterbitkan 2015-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome

    Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome oleh Sarah de Jong, Anita de Breuk, Bjorn Bakker, Suresh Katti, Carel B. Hoyng, Sara C. Nilsson, Anna M. Blom, Lambert P. van den Heuvel, Lambert P. van den Heuvel, Lambert P. van den Heuvel, Anneke I. den Hollander, Anneke I. den Hollander, Elena B. Volokhina, Elena B. Volokhina, Elena B. Volokhina

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Generation and characterization of human induced pluripotent stem cells (iPSCs) from three patients with age-related macular degeneration carrying rare variants in the CFH gene

    Generation and characterization of human induced pluripotent stem cells (iPSCs) from three patients with age-related macular degeneration carrying rare variants in the CFH gene oleh Louet Koolen, Giuliana Gagliardi, Sofie C.A. ten Brink, Anita de Breuk, Thomas J. Heesterbeek, Carel B. Hoyng, Silvia Albert, Anneke I. den Hollander

    Diterbitkan 2022-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    Generation of an iPSC line (SCTCi014-A) and isogenic control line (SCTCi014-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene

    Generation of an iPSC line (SCTCi014-A) and isogenic control line (SCTCi014-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene oleh Sarah de Jong, Louet Koolen, Irene Vázquez-Domínguez, Anita de Breuk, Silvia Albert, Carel B. Hoyng, Suresh Katti, Anneke I. den Hollander, Alejandro Garanto

    Diterbitkan 2022-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    Generation of an iPSC line (SCTCi015-A) and isogenic control line (SCTCi015-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene

    Generation of an iPSC line (SCTCi015-A) and isogenic control line (SCTCi015-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene oleh Sarah de Jong, Louet Koolen, Irene Vázquez-Domínguez, Anita de Breuk, Silvia Albert, Carel B. Hoyng, Suresh Katti, Anneke I. den Hollander, Alejandro Garanto

    Diterbitkan 2022-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    Generation and characterization of human induced pluripotent stem cells (iPSCs) from three individuals without age-related macular degeneration

    Generation and characterization of human induced pluripotent stem cells (iPSCs) from three individuals without age-related macular degeneration oleh Louet Koolen, Giuliana Gagliardi, Sofie C.A. ten Brink, Anita de Breuk, Thomas J. Heesterbeek, Carel B. Hoyng, Silvia Albert, Anneke I. den Hollander

    Diterbitkan 2022-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    ERAP2 Increases the Abundance of a Peptide Submotif Highly Selective for the Birdshot Uveitis-Associated HLA-A29

    ERAP2 Increases the Abundance of a Peptide Submotif Highly Selective for the Birdshot Uveitis-Associated HLA-A29 oleh Wouter J. Venema, Wouter J. Venema, Sanne Hiddingh, Sanne Hiddingh, Joke H. de Boer, Frans H. J. Claas, Arend Mulder, Anneke I. den Hollander, Anneke I. den Hollander, Efstratios Stratikos, Siranush Sarkizova, Siranush Sarkizova, Lars T. van der Veken, George M. C. Janssen, Peter A. van Veelen, Jonas J. W. Kuiper, Jonas J. W. Kuiper

    Diterbitkan 2021-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels.

    Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels. oleh Tina Ristau, Constantin Paun, Lebriz Ersoy, Moritz Hahn, Yara Lechanteur, Carel Hoyng, Eiko K de Jong, Mohamed R Daha, Bernd Kirchhof, Anneke I den Hollander, Sascha Fauser

    Diterbitkan 2014-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    Systemic complement activation levels in Stargardt disease.

    Systemic complement activation levels in Stargardt disease. oleh Patty P A Dhooge, Esmee H Runhart, Catherina H Z Li, Corrie M de Kat Angelino, Carel B Hoyng, Renate G van der Molen, Anneke I den Hollander

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  18. 18
    Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma.

    Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma. oleh Humaira Ayub, Shazia Micheal, Farah Akhtar, Muhammad Imran Khan, Shaheena Bashir, Nadia K Waheed, Mahmood Ali, Frederieke E Schoenmaker-Koller, Sobia Shafique, Raheel Qamar, Anneke I den Hollander

    Diterbitkan 2014-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  19. 19
    Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular Degeneration.

    Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular Degeneration. oleh Nicole T M Saksens, Yara T E Lechanteur, Sanne K Verbakel, Joannes M M Groenewoud, Mohamed R Daha, Tina Schick, Sascha Fauser, Camiel J F Boon, Carel B Hoyng, Anneke I den Hollander

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  20. 20
    Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes

    Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and T... oleh Louise F. Porter, Neil Saptarshi, Yongxiang Fang, Sonika Rathi, Anneke I. den Hollander, Eiko K. de Jong, Simon J. Clark, Paul N. Bishop, Timothy W. Olsen, Triantafillos Liloglou, Venkata R. M. Chavali, Luminita Paraoan

    Diterbitkan 2019-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: