Search Results - Laura Russell

  • Showing 1 - 13 results of 13
Refine Results
  1. 1
    Axial mesodermal dysplasia spectrum

    Axial mesodermal dysplasia spectrum by Laura Russell, David D. Weaver, Marilyn J. Bull

    Published 2020
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    The determination of stratum corneum thickness An alternative approach

    The determination of stratum corneum thickness An alternative approach by Laura Russell, Sandra Wiedersberg, M. Begoña Delgado‐Charro

    Published 2008
    Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Thyroid Hormone Signalling Genes Are Regulated by Photoperiod in the Hypothalamus of F344 Rats

    Thyroid Hormone Signalling Genes Are Regulated by Photoperiod in the Hypothalamus of F344 Rats by Alexander Ross, Gisela Helfer, Laura Russell, Veerle Darras, Peter J. Morgan

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

    Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption by Daniel Sanghoon Shin, Sang Hee Min, Laura Russell, Rongbao Zhao, András Fiser, I. David Goldman

    Published 2010
    Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Pharmacogenomics in the era of next generation sequencing – from byte to bedside

    Pharmacogenomics in the era of next generation sequencing – from byte to bedside by Laura Russell, Yitian Zhou, Ahmed A. Almousa, Jasleen K. Sodhi, Chukwunonso K. Nwabufo, Volker M. Lauschke

    Published 2021
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  6. 6
    Photoperiod Regulates Vitamin A and Wnt/β-Catenin Signaling in F344 Rats

    Photoperiod Regulates Vitamin A and Wnt/β-Catenin Signaling in F344 Rats by Gisela Helfer, Alexander Ross, Laura Russell, Lynn Thomson, Kirsty Shearer, Timothy Goodman, Peter McCaffery, Peter J. Morgan

    Published 2011
    Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    FOXP3 Forkhead Domain Mutation and Regulatory T Cells in the IPEX Syndrome

    FOXP3 Forkhead Domain Mutation and Regulatory T Cells in the IPEX Syndrome by Eva d’Hennezel, Moshe Ben‐Shoshan, Hans D. Ochs, Troy R. Torgerson, Laura Russell, Christine Lejtenyi, Francisco Noya, Nada Jabado, Bruce Mazer, Ciriaco A. Piccirillo

    Published 2009
    Get full text Get full text
    Carta
    Save to List
    Saved in:
  8. 8
    Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

    Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome by Gabriele Richard, Fatima Rouan, Colin E. Willoughby, Nkecha Brown, Pil Joong Chung, Markku Ryynänen, Ethylin Wang Jabs, Sherri J. Bale, John J. DiGiovanna, Jouni Uitto, Laura Russell

    Published 2002
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

    Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth by Nicole Revençu, Laurence M. Boon, A. Dompmartin, Paul N.M.A. Rieu, W Busch, Josée Dubois, Francesca Forzano, Johanna M. van Hagen, Sara Halbach, A. Kuechler, A.M.A. Lachmeijer, Jyrki Lähde, Laura Russell, K. O. J. Simola, John B. Mulliken, Miikka Vikkula

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

    Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth by Johanna M. Huusko, Minna K. Karjalainen, Britney E. Graham, Ge Zhang, Emily Farrow, Neil Miller, Bo Jacobsson, Haley Eidem, Jeffrey C. Murray, Bruce Bedell, Patrick Breheny, Noah Brown, Frans Bodker, Nadia K. Litterman, Panpan Jiang, Laura Russell, David A. Hinds, Youna Hu, Antonis Rokas, Kari Teramo, Kaare Christensen, Scott M. Williams, Mika Rämet, Stephen F. Kingsmore, Kelli K. Ryckman, Mikko Hallman, Louis J. Muglia

    Published 2018
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    A Clinical Program for Transgender and Gender-Diverse Neurodiverse/Autistic Adolescents Developed through Community-Based Participatory Design

    A Clinical Program for Transgender and Gender-Diverse Neurodiverse/Autistic Adolescents Developed through Community-Based Participatory Design by John F. Strang, Megan Knauss, Anna I. R. van der Miesen, Jenifer K. McGuire, Lauren Kenworthy, Reid Caplan, Andrew J. Freeman, Eleonora Sadikova, Zosia Zaks, Noor Pervez, Anouk Balleur, D. W. Rowlands, Ely Sibarium, Laura Willing, Marissa A. McCool, Randall D. Ehrbar, Shannon E. Wyss, Harriette Wimms, Joshua H. L. Tobing, J. Graham Thomas, Julie Austen, Elyse Pine-Twaddell, April Dawn Griffin, Aron Janssen, Veronica Gómez-Lobo, Abigail Brandt, Colleen Morgan, Haley Meagher, Dena Gohari, Laura Kirby, Laura Russell, Meredith D. Powers, Laura G. Anthony

    Published 2020
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

    Genetic Associations with Gestational Duration and Spontaneous Preterm Birth by Ge Zhang, Bjarke Feenstra, Jonas Bacelis, Xueping Liu, Lisa M. Muglia, Julius Juodakis, Daniel E. Miller, Nadia K. Litterman, Panpan Jiang, Laura Russell, David A. Hinds, Youna Hu, Matthew T. Weirauch, Xiaoting Chen, Arun R. Chavan, Günter P. Wagner, Mihaela Pavličev, Mauris C. Nnamani, Jamie Maziarz, Minna K. Karjalainen, Mika Rämet, Verena Sengpiel, Frank Geller, Heather A. Boyd, Aarno Palotie, Allison M. Momany, Bruce Bedell, Kelli K. Ryckman, Johanna M. Huusko, Carmy Forney, Leah C. Kottyan, Mikko Hallman, Kari Teramo, Ellen A. Nøhr, George Davey Smith, Mads Melbye, Bo Jacobsson, Louis J. Muglia

    Published 2017
    Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848

    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848 by Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Sherrell Johnson, Meng-Chang Hsiao, Zhenbin Chen, Meena Balasubramanian, Christopher Barnett, Troy A. Becker, Shay Ben‐Shachar, Débora Romeo Bertola, Jaishri O. Blakeley, Emma Burkitt‐Wright, Alison Callaway, Melissa Crenshaw, Karin Soares Cunha, Mitch Cunningham, Daniela D’Agostino, Karin Dahan, Alessandro De Luca, Anne Destrèe, Radhika Dhamija, Marica Eoli, D. Gareth Evans, Patricia Galvin‐Parton, Jaya K. George‐Abraham, Karen W. Gripp, José Guevara-Campos, Neil A. Hanchard, Concepción Hernández-Chico, LaDonna Immken, Sandra Janssens, Kristi Jones, Beth Keena, Aaina Kochhar, Jan Liebelt, Arelis Martir-Negron, Maurice J. Mahoney, Isabelle Maystadt, Carey McDougall, Meriel McEntagart, Nancy J. Mendelsohn, David T. Miller, Geert Mortier, Jenny Morton, John Pappas, Scott R. Plotkin, Dinel Pond, Kenneth N. Rosenbaum, Karol Rubin, Laura Russell, Lane Rutledge, Veronica Saletti, Rhonda Schonberg, Allison Schreiber, Meredith Seidel, Elizabeth Siqveland, David W. Stockton, Eva Trevisson, Nicole J. Ullrich, Meena Upadhyaya, Rick van Minkelen, Hélène Verhelst, Margaret R. Wallace, Yoon Sim Yap, Elaine H. Zackai, Jonathan Zonana, Vickie Zurcher, Kathleen Claes, Yolanda Martín, Bruce R. Korf, Eric Legius, Ludwine Messiaen

    Published 2017
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: