Хайлтын үр дүнгүүд - Trembath, Richard

Genetics -н Trembath, Richard

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Causes of Diabetes: Genetic and Environmental Factors -н Trembath, Richard

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Inherited Disorders of the Thyroid System -н Trembath, Richard

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Genetic Mechanisms and Mental Retardation -н Trembath, Richard C

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Psoriasis and other complex trait dermatoses: from loci to functional pathways -н Capon, Francesca, Burden, A David, Trembath, Richard C, Barker, Jonathan N

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Bone Morphogenetic Protein (BMP) and Activin Type II Receptors Balance BMP9 Signals Mediated by Activin Receptor-like Kinase-1 in Human Pulmonary Artery Endothelial Cells -н Upton, Paul D., Davies, Rachel J., Trembath, Richard C., Morrell, Nicholas W.

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Functional analysis of the RNF114 psoriasis susceptibility gene implicates innate immune responses to double-stranded RNA in disease pathogenesis -н Bijlmakers, Marie-José, Kanneganti, Seshu K., Barker, Jonathan N., Trembath, Richard C., Capon, Francesca

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A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption -н Meyer, Esther, Kurian, Manju A., Pasha, Shanaz, Trembath, Richard C., Cole, Trevor, Maher, Eamonn R.

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Genetic Association Analysis Using Data from Triads and Unrelated Subjects -н Epstein, Michael P., Veal, Colin D., Trembath, Richard C., Barker, Jonathan N. W. N., Li, Chun, Satten, Glen A.

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Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E -н Johnson, David, Kan, Shih-hsin, Oldridge, Michael, Trembath, Richard C., Roche, Philippe, Esnouf, Robert M., Giele, Henk, Wilkie, Andrew O. M.

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SUN1 Interacts with Nuclear Lamin A and Cytoplasmic Nesprins To Provide a Physical Connection between the Nuclear Lamina and the Cytoskeleton -н Haque, Farhana, Lloyd, David J., Smallwood, Dawn T., Dent, Carolyn L., Shanahan, Catherine M., Fry, Andrew M., Trembath, Richard C., Shackleton, Sue

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Whole Exome Sequence Analysis Provides Novel Insights into the Genetic Framework of Childhood-Onset Pulmonary Arterial Hypertension -н Gelinas, Simone M., Benson, Clare E., Khan, Mohammed A., Berger, Rolf M. F., Trembath, Richard C., Machado, Rajiv D., Southgate, Laura

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Initiation codon mutation in βB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract -н Meyer, Esther, Rahman, Fatimah, Owens, Jessica, Pasha, Shanaz, Morgan, Neil V., Trembath, Richard C., Stone, Edwin M., Moore, Anthony T., Maher, Eamonn R.

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Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis -н Knight, Jo, Spain, Sarah L., Capon, Francesca, Hayday, Adrian, Nestle, Frank O., Clop, Alex, Barker, Jonathan N., Weale, Michael E., Trembath, Richard C.

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

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The Psoriasis Risk Allele HLA-C*06:02 Shows Evidence of Association with Chronic or Recurrent Streptococcal Tonsillitis -н Haapasalo, Karita, Koskinen, Lotta L. E., Suvilehto, Jari, Jousilahti, Pekka, Wolin, Annika, Suomela, Sari, Trembath, Richard, Barker, Jonathan, Vuopio, Jaana, Kere, Juha, Jokiranta, T. Sakari, Saavalainen, Päivi

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The IL23R R381Q Gene Variant Protects against Immune-Mediated Diseases by Impairing IL-23-Induced Th17 Effector Response in Humans -н Di Meglio, Paola, Di Cesare, Antonella, Laggner, Ute, Chu, Chung-Ching, Napolitano, Luca, Villanova, Federica, Tosi, Isabella, Capon, Francesca, Trembath, Richard C., Peris, Ketty, Nestle, Frank O.

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Demographic features, BMPR2 status and outcomes in distal chronic thromboembolic pulmonary hypertension -н Suntharalingam, Jay, Machado, Rajiv D, Sharples, Linda D, Toshner, Mark R, Sheares, Karen K, Hughes, Rodney J, Jenkins, David P, Trembath, Richard C, Morrell, Nicholas W, Pepke‐Zaba, Joanna

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Genetics and Genomics of Pulmonary Arterial Hypertension -н Machado, Rajiv D., Eickelberg, Oliver, Elliott, Greg, Geraci, Mark W., Hanaoka, Masayuki, Loyd, James E., Newman, John H., Phillips, John A., Soubrier, Florent, Trembath, Richard C., Chung, Wendy K.

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Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus -н Veal, Colin D., Capon, Francesca, Allen, Michael H., Heath, Emma K., Evans, Julie C., Jones, Andrew, Patel, Shanta, Burden, David, Tillman, David, Barker, Jonathan N. W. N., Trembath, Richard C.

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