檢索結果 - Brendan Lee

Refine Results
  1. 1
    Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency

    Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency 由 Fernando Scaglia, Brendan Lee

    出版 2006
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  2. 2
    NOTCHing the bone: Insights into multi-functionality

    NOTCHing the bone: Insights into multi-functionality 由 Feyza Engin, Brendan Lee

    出版 2009
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  3. 3
    Alteration of Notch signaling in skeletal development and disease

    Alteration of Notch signaling in skeletal development and disease 由 Jianning Tao, Shan Chen, Brendan Lee

    出版 2010
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  4. 4
    Osteogenesis imperfecta: advancements in genetics and treatment

    Osteogenesis imperfecta: advancements in genetics and treatment 由 Vittoria Rossi, Brendan Lee, Ronit Marom

    出版 2019
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  5. 5
    Argininosuccinate lyase deficiency

    Argininosuccinate lyase deficiency 由 Sandesh C.S. Nagamani, Ayelet Erez, Brendan Lee

    出版 2012
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  6. 6
    Genotype–Phenotype Correlation — Promiscuity in the Era of Next-Generation Sequencing

    Genotype–Phenotype Correlation — Promiscuity in the Era of Next-Generation Sequencing 由 James T. Lu, Philippe M. Campeau, Brendan Lee

    出版 2014
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    Argininosuccinate lyase deficiency—Argininosuccinic aciduria and beyond

    Argininosuccinate lyase deficiency—Argininosuccinic aciduria and beyond 由 Ayelet Erez, Sandesh C. Sreenath Nagamani, Brendan Lee

    出版 2011
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  8. 8
    Genetic causes and mechanisms of Osteogenesis Imperfecta

    Genetic causes and mechanisms of Osteogenesis Imperfecta 由 Joohyun Lim, Ingo Grafe, Stefanie Alexander, Brendan Lee

    出版 2017
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  9. 9
    Diagnosis, symptoms, frequency and mortality of 260 patients with urea cycle disorders from a 21‐year, multicentre study of acute hyperammonaemic episodes

    Diagnosis, symptoms, frequency and mortality of 260 patients with urea cycle disorders from a 21‐year, multicentre study of acute hyperammonaemic episodes 由 Marshall Summar, Dries Dobbelaere, Saul W. Brusilow, Brendan Lee

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis

    Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis 由 Jennifer Zieba, Yi-Ting Chen, Brendan Lee, Yangjin Bae

    出版 2020
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  11. 11
    Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII

    Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII 由 Chuhong Hu, G. Racel, Masataka Suzuki, Brendan Lee, Gerald S. Lipshutz

    出版 2011
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  12. 12
    Glutamine: precursor or nitrogen donor for citrulline synthesis?

    Glutamine: precursor or nitrogen donor for citrulline synthesis? 由 Juan C. Marini, Inka C. Didelija, Leticia Castillo, Brendan Lee

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    Insights into the Pathogenesis and Treatment of Cancer from Inborn Errors of Metabolism

    Insights into the Pathogenesis and Treatment of Cancer from Inborn Errors of Metabolism 由 Ayelet Erez, Oleg A. Shchelochkov, Sharon E. Plon, Fernando Scaglia, Brendan Lee

    出版 2011
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  14. 14
    Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte–specific expression in vivo

    Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte–specific expression in vivo 由 Qiping Zheng, Guang Zhou, Roy Morello, Yuqing Chen, Xavier Garcia-Rojas, Brendan Lee

    出版 2003
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    <i>WDR35</i> mutation in siblings with Sensenbrenner syndrome: A ciliopathy with variable phenotype

    <i>WDR35</i> mutation in siblings with Sensenbrenner syndrome: A ciliopathy with variable phenotype 由 Carlos A. Bacino, Shweta U. Dhar, Nicola Brunetti‐Pierri, Brendan Lee, Penelope E. Bonnen

    出版 2012
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  16. 16
    Osteosclerosis owing to Notch gain of function is solely Rbpj-dependent

    Osteosclerosis owing to Notch gain of function is solely Rbpj-dependent 由 Jianning Tao, Shan Chen, Tao Yang, Brian Dawson, Elda Munivez, Terry Bertin, Brendan Lee

    出版 2010
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  17. 17
    Feasibility of Magnetic Resonance Fingerprinting on Aging MRI Hardware

    Feasibility of Magnetic Resonance Fingerprinting on Aging MRI Hardware 由 Eck, Brendan Lee, Liu, Kecheng, Lo, Wei-ching, Jiang, Yun, Gulani, Vikas, Seiberlich, Nicole

    出版 2021
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  18. 18
    Interaction of TGFβ and BMP Signaling Pathways during Chondrogenesis

    Interaction of TGFβ and BMP Signaling Pathways during Chondrogenesis 由 Bettina G. Keller, Tao Yang, Yuqing Chen, Elda Munivez, Terry Bertin, Bernhard Zabel, Brendan Lee

    出版 2011
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  19. 19
    Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome

    Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome 由 Dobrawa Napierala, Kathy Sam, Roy Morello, Qiping Zheng, Elda Munivez, Ramesh A. Shivdasani, Brendan Lee

    出版 2008
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  20. 20
    TGF-β Family Signaling in Mesenchymal Differentiation

    TGF-β Family Signaling in Mesenchymal Differentiation 由 Ingo Grafe, Stefanie Alexander, Jonathan Peterson, Taylor Nicholas Snider, Benjamin Lévi, Brendan Lee, Yuji Mishina

    出版 2017
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:

檢索工具: