Bilaketaren emaitzak - William C. Nichols

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  1. 1
    von Willebrand Disease

    von Willebrand Disease nork William C. Nichols, David Ginsburg

    Argitaratua 1997
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  2. 2
    Midkine Is Regulated by Hypoxia and Causes Pulmonary Vascular Remodeling

    Midkine Is Regulated by Hypoxia and Causes Pulmonary Vascular Remodeling nork Paul R. Reynolds, Michael L. Mucenski, Timothy D. Le Cras, William C. Nichols, Jeffrey A. Whitsett

    Argitaratua 2004
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  3. 3
    Mannose-dependent Endoplasmic Reticulum (ER)-Golgi Intermediate Compartment-53-mediated ER to Golgi Trafficking of Coagulation Factors V and VIII

    Mannose-dependent Endoplasmic Reticulum (ER)-Golgi Intermediate Compartment-53-mediated ER to Golgi Trafficking of Coagulation Factors V and VIII nork Micheline J. Moussalli, Steven W. Pipe, Hans-Peter Hauri, William C. Nichols, David Ginsburg, Randal J. Kaufman

    Argitaratua 1999
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  4. 4
    Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations

    Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations nork Nathan Pankratz, William C. Nichols, Sean K. Uniacke, Cheryl Halter, Alice Rudolph, Cliff Shults, P. Michael Conneally, Tatiana Foroud

    Argitaratua 2002
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  5. 5
    Genetics and precision genomics approaches to pulmonary hypertension

    Genetics and precision genomics approaches to pulmonary hypertension nork Eric D. Austin, Micheala A. Aldred, Mona Alotaibi, Stefan Gräf, William C. Nichols, Richard C. Trembath, Wendy K. Chung

    Argitaratua 2024
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  6. 6
    Tet Methylcytosine Dioxygenase 2 (<scp><i>TET2</i></scp>) Mutation Drives a Global Hypermethylation Signature in Patients With Pulmonary Arterial Hypertension (<scp>PAH</scp>): Correlation With Altered Gene Expression Relevant to a Common T Cell Phenotype

    Tet Methylcytosine Dioxygenase 2 (<scp><i>TET2</i></scp>) Mutation Drives a Global Hypermethylation Signature in Patients With Pulmonary Arterial Hypertension (<scp>PAH</scp>): Cor... nork Charles C.T. Hindmarch, François Potus, Ruaa Al‐Qazazi, Benjamin Ott, William C. Nichols, Michael J. Rauh, Stephen L. Archer

    Argitaratua 2025
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  7. 7
    Multiple step pattern as a biomarker in Parkinson disease

    Multiple step pattern as a biomarker in Parkinson disease nork Tanya Blekher, Marjorie Weaver, Jason Rupp, William C. Nichols, Siu L. Hui, Jacqueline S. Gray, Robert D. Yee, Joanne Wojcieszek, Tatiana Foroud

    Argitaratua 2009
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  8. 8
    Racial and ethnic differences in pulmonary arterial hypertension

    Racial and ethnic differences in pulmonary arterial hypertension nork Nadine Al‐Naamani, Jessica K. Paulus, Kari E. Roberts, Michael W. Pauciulo, Katie A. Lutz, William C. Nichols, Steven M. Kawut

    Argitaratua 2017
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  9. 9
    The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.

    The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain. nork Kathleen A. Cooney, William C. Nichols, M E Bruck, Wadie F. Bahou, Amy D. Shapiro, Ejw Bowie, H R Gralnick, David Ginsburg

    Argitaratua 1991
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  10. 10
    <i>Parkin</i> dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

    <i>Parkin</i> dosage mutations have greater pathogenicity in familial PD than simple sequence mutations nork Nathan Pankratz, Diane Kissell, Michael W. Pauciulo, C. A. Halter, Alice Rudolph, Ronald F. Pfeiffer, Karen Marder, Tatiana Foroud, William C. Nichols

    Argitaratua 2009
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  11. 11
    Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

    Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families nork Nathan Pankratz, William C. Nichols, Sean K. Uniacke, Cheryl Halter, Jill R. Murrell, Alice Rudolph, Clifford W. Shults, P. Michael Conneally, Tatiana Foroud

    Argitaratua 2003
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  12. 12
    Genetics and genomics of pulmonary arterial hypertension

    Genetics and genomics of pulmonary arterial hypertension nork Nicholas W. Morrell, Micheala A. Aldred, Wendy K. Chung, C. Gregory Elliott, William C. Nichols, Florent Soubrier, Richard C. Trembath, James E. Loyd

    Argitaratua 2018
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  13. 13
    A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia.

    A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia. nork A C Moses, Harold N. Rosen, David E. Moller, S. Tsuzaki, James E. Haddow, Jennifer Lawlor, J. J. Liepnieks, William C. Nichols, M D Benson

    Argitaratua 1990
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  14. 14
    Mutations in <i>GBA</i> are associated with familial Parkinson disease susceptibility and age at onset

    Mutations in <i>GBA</i> are associated with familial Parkinson disease susceptibility and age at onset nork William C. Nichols, Nathan Pankratz, D. K. Marek, Michael W. Pauciulo, Veronika E. Elsaesser, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer, Tatiana Foroud

    Argitaratua 2008
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  15. 15
    Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII

    Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII nork William C. Nichols, Uri Seligsohn, Ariella Zivelin, Valeri H. Terry, Colette E Hertel, Matthew Wheatley, Micheline J. Moussalli, Hans-Peter Hauri, N. Ciavarella, Randal J. Kaufman, David Ginsburg

    Argitaratua 1998
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  16. 16
    High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension

    High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension nork Nambirajan Sundaram, Anitaben Tailor, Laurel Mendelsohn, Janaka Wansapura, Xunde Wang, Tomoyasu Higashimoto, Michael W. Pauciulo, William Gottliebson, Vijay K. Kalra, William C. Nichols, Gregory J. Kato, Punam Malik

    Argitaratua 2010
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  17. 17
    Genomewide association study for susceptibility genes contributing to familial Parkinson disease

    Genomewide association study for susceptibility genes contributing to familial Parkinson disease nork Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Anita L. DeStefano, Cheryl Halter, Elizabeth Pugh, Kimberly F. Doheny, James F. Gusella, William C. Nichols, Tatiana Foroud, Richard H. Myers

    Argitaratua 2008
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  18. 18
    High Frequency of <i>BMPR2</i> Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension

    High Frequency of <i>BMPR2</i> Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension nork Joy D. Cogan, Michael W. Pauciulo, Amy P. Batchman, Melissa Prince, Ivan M. Robbins, Lora K. Hedges, Krista C. Stanton, Lisa Wheeler, John A. Phillips, James E. Loyd, William C. Nichols

    Argitaratua 2006
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  19. 19
    Frequency of <i>GBA</i> Variants in Autopsy‐proven Multiple System Atrophy

    Frequency of <i>GBA</i> Variants in Autopsy‐proven Multiple System Atrophy nork Miriam Sklerov, Un Jung Kang, Christopher Liong, Lorraine N. Clark, Karen Marder, Michael W. Pauciulo, William C. Nichols, Wendy K. Chung, Lawrence S. Honig, Etty Cortés, Jean Paul Vonsattel, Roy N. Alcalay

    Argitaratua 2017
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  20. 20
    Genomewide association study for onset age in Parkinson disease

    Genomewide association study for onset age in Parkinson disease nork Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio Mariani, Anita L. DeStefano, Cheryl Halter, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud

    Argitaratua 2009
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