Хайлтын үр дүнгүүд - John McCarthy

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  1. 1
    Attitudes toward Individuals Who Use Augmentative and Alternative Communication: Research Review

    Attitudes toward Individuals Who Use Augmentative and Alternative Communication: Research Review -н John McCarthy, Janice Light

    Хэвлэсэн 2005
    Бүрэн текст авах
    Artigo
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  2. 2
    Evidence that the cycloheximide-sensitive site of adrenocorticotropic hormone action is in the mitochondrion. Changes in pregnenolone formation, cholesterol content, and the electron paramagnetic resonance spectra of cytochrome P-450.

    Evidence that the cycloheximide-sensitive site of adrenocorticotropic hormone action is in the mitochondrion. Changes in pregnenolone formation, cholesterol content, and the electr... -н E R Simpson, John McCarthy, Jerry A. Peterson

    Хэвлэсэн 1978
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    Artigo
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  3. 3
    Evaluation of Plasma Erythropoietic-Stimulating Factors in Anemic Uremic Patients

    Evaluation of Plasma Erythropoietic-Stimulating Factors in Anemic Uremic Patients -н N. I. Gallagher, John McCarthy, Kathleen T. Hart, Robert D. Lange

    Хэвлэсэн 1959
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    Artigo
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  4. 4
    Rat P450<sub>17α</sub>from Testis: Characterization of a Full-Length cDNA Encoding a Unique Steroid Hydroxylase Capable of Catalyzing Both Δ<sup>4</sup>- and Δ<sup>5</sup>-Steroid-17,20-Lyase Reactions

    Rat P450<sub>17α</sub>from Testis: Characterization of a Full-Length cDNA Encoding a Unique Steroid Hydroxylase Capable of Catalyzing Both Δ<sup>4</sup>- and Δ<sup>5</sup>-Steroid-... -н H. Richard Fevold, Matthew C. Lorence, John McCarthy, John M. Trant, Masaaki Kagimoto, Michael R. Waterman, J. Ian Mason

    Хэвлэсэн 1989
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    Artigo
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  5. 5
    A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy

    A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy -н Alan D. Irvine, C. M. Coleman, Jonathan E. Moore, Ole Swensson, Steven Morgan, John McCarthy, Frances J.D. Smith, Graeme Black, W.H. Irwin McLean

    Хэвлэсэн 2002
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    Carta
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  6. 6
    Linkage of Familial Hibernian Fever to Chromosome 12p13

    Linkage of Familial Hibernian Fever to Chromosome 12p13 -н Michael McDermott, B Ogunkolade, Elizabeth McDermott, Lisa C. Jones, Ying Wan, Kathleen A. Quane, John McCarthy, Mark Phelan, Michael G. Molloy, Richard J. Powell, Christopher I. Amos, G. A. Hitman

    Хэвлэсэн 1998
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    Artigo
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  7. 7
    Schaaf‐Yang syndrome overview: Report of 78 individuals

    Schaaf‐Yang syndrome overview: Report of 78 individuals -н John McCarthy, Philip J. Lupo, Erin Kovar, Megan Rech, Bret L. Bostwick, Daryl A. Scott, Katerina Kraft, Tony Roscioli, Joel Charrow, Samantha A. Schrier Vergano, Edward J. Lose, Robert Smiegel, Yves Lacassie, Christian P. Schaaf

    Хэвлэсэн 2018
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    Artigo
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  8. 8
    Phenotypic expansion of <scp>Bosch–Boonstra–Schaaf</scp> optic atrophy syndrome and further evidence for genotype–phenotype correlations

    Phenotypic expansion of <scp>Bosch–Boonstra–Schaaf</scp> optic atrophy syndrome and further evidence for genotype–phenotype correlations -н Megan Rech, John McCarthy, Chun‐An Chen, Jane C. Edmond, Veeral S. Shah, Daniëlle G.M. Bosch, Gerard T. Berry, Linford Williams, Suneeta Madan‐Khetarpal, Dmitriy Niyazov, Charles Shaw‐Smith, Erin Kovar, Philip J. Lupo, Christian P. Schaaf

    Хэвлэсэн 2020
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    Artigo
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  9. 9
    Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes

    Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes -н Michael McDermott, Ivona Aksentijevich, Jérôme Galon, Elizabeth McDermott, B Ogunkolade, Michael Centola, Elizabeth Mansfield, Massimo Gadina, Leena Karenko, Tom Pettersson, John McCarthy, David M. Frucht, Martin Aringer, Yelizaveta Torosyan, Anna‐Maija Teppo, Meredith Wilson, H.Mehmet Karaarslan, Ying Wan, Ian Todd, Geryl Wood, Ryan Schlimgen, Thisum R. Kumarajeewa, Sheldon M. Cooper, John P. Vella, Christopher I. Amos, John C. Mulley, Kathleen A. Quane, Michael G. Molloy, Annamari Ranki, Richard J. Powell, G. A. Hitman, John J. O’Shea, Daniel L. Kastner

    Хэвлэсэн 1999
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    Artigo
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  10. 10
    Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies

    Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies -н Michael D. Fountain, David S. Oleson, Megan Rech, Lara Segebrecht, Jill V. Hunter, John McCarthy, Philip J. Lupo, Manuel Holtgrewe, Rocio Moran, Jill A. Rosenfeld, Bertrand Isidor, Cédric Le Caignec, Margarita Sáenz, Robert C. Pedersen, Thomas M. Morgan, Jean P. Pfotenhauer, Fan Xia, Weimin Bi, Sung-Hae L. Kang, Ankita Patel, Ian D. Krantz, Sarah E. Raible, Wendy E. Smith, Ingrid Cristian, Erin Torti, Jane Juusola, Francisca Millan, Ingrid M. Wentzensen, Richard Person, Sébastien Küry, Stéphane Bézieau, Kévin Uguen, Claude Férec, Arnold Münnich, Mieke M. van Haelst, Klaske D. Lichtenbelt, Koen L.I. van Gassen, Tanner Hagelstrom, Aditi Chawla, Denise Perry, Ryan J. Taft, Marilyn C. Jones, Diane Masser‐Frye, David A. Dyment, Sunita Venkateswaran, Chumei Li, Luis Escobar, Denise Horn, Rebecca C. Spillmann, Loren D.M. Peña, Jolanta Wierzba, Tim M. Strom, Ilaria Parenti, Frank J. Kaiser, Nadja Ehmke, Christian P. Schaaf

    Хэвлэсэн 2019
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    Artigo
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