Torthaí cuardaigh - Frank Baas
- 1 - 20 toradh as 100 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Oligomer-specific Aβ toxicity in cell models is mediated by selective uptake de réir Sidhartha M. Chafekar, Frank Baas, Wiep Scheper
Foilsithe / Cruthaithe 2008Artigo -
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Classification, diagnosis and potential mechanisms in Pontocerebellar Hypoplasia de réir Yasmin Namavar, P. G. Barth, Bwee Tien Poll‐The, Frank Baas
Foilsithe / Cruthaithe 2011Revisão -
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What’s new in pontocerebellar hypoplasia? An update on genes and subtypes de réir Tessa van Dijk, Frank Baas, P. G. Barth, Bwee Tien Poll‐The
Foilsithe / Cruthaithe 2018Revisão -
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Inhibition of the Membrane Attack Complex of the Complement System Reduces Secondary Neuroaxonal Loss and Promotes Neurologic Recovery after Traumatic Brain Injury in Mice de réir Kees Fluiter, Anne Loes Opperhuizen, B. Paul Morgan, Frank Baas, Valeria Ramaglia
Foilsithe / Cruthaithe 2014Artigo -
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Complement activation at the motor end-plates in amyotrophic lateral sclerosis de réir Nawal Bahia El Idrissi, Sanne Bosch, Valeria Ramaglia, Eleonora Aronica, Frank Baas, Dirk Troost
Foilsithe / Cruthaithe 2016Artigo -
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Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings de réir Janneke Zinkstok, Odette de Wilde, Thérèse van Amelsvoort, Michael W.T. Tanck, Frank Baas, Don Linszen
Foilsithe / Cruthaithe 2007Artigo -
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The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb de réir Frank Baas, Gert‐Jan B. van Ommen, Hennie Bikker, Annika C. Arnberg, Jan J. M. de Vijlder
Foilsithe / Cruthaithe 1986Artigo -
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Oral high dose ascorbic acid treatment for one year in young CMT1A patients: a randomised, double-blind, placebo-controlled phase II trial de réir Camiel Verhamme, Rob J. de Haan, Marinus Vermeulen, Frank Baas, Marianne de Visser, Ivo N. van Schaik
Foilsithe / Cruthaithe 2009Artigo -
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Germline Mutation of INI1/SMARCB1 in Familial Schwannomatosis de réir Theo J.M. Hulsebos, Astrid S. Plomp, Ruud A. Wolterman, Els C. Robanus-Maandag, Frank Baas, Pieter Wesseling
Foilsithe / Cruthaithe 2007Artigo -
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Genes differentially expressed in medulloblastoma and fetal brain de réir Erna Michiels, Esmée Oussoren, Marjon van Groenigen, Erwin Pauws, Patrick M. Bossuyt, P.A. Voûte, Frank Baas
Foilsithe / Cruthaithe 1999Artigo -
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Branched KLVFF Tetramers Strongly Potentiate Inhibition of β‐Amyloid Aggregation de réir Sidhartha M. Chafekar, Hinke Malda, Maarten Merkx, E. W. Meijer, David Viertl, Hilal A. Lashuel, Frank Baas, Wiep Scheper
Foilsithe / Cruthaithe 2007Artigo -
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Abnormal heart rate and body temperature in mice lacking thyroid hormone receptor alpha 1 de réir Lilian Wikström, Catarina Johansson, Carmen Saltó, Carrolee Barlow, Ángel Campos‐Barros, Frank Baas, Douglas Forrest, Peter Thorén, Björn Vennström
Foilsithe / Cruthaithe 1998Artigo -
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The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype de réir Casper Jansen, Mark Head, Willem A. van Gool, Frank Baas, Helen Yull, James W. Ironside, Annemieke J.M. Rozemüller
Foilsithe / Cruthaithe 2010Artigo -
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The human mdr3 gene encodes a novel P-glycoprotein homologue and gives rise to alternatively spliced mRNAs in liver. de réir Alexander M. van der Bliek, Frank Baas, T. Ten Houte de Lange, Patricia M. Kooiman, T Van der Velde-Koerts, Piet Borst
Foilsithe / Cruthaithe 1987Artigo -
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Striatal Dopamine Transporter Availability Associated with Polymorphisms in the Dopamine Transporter Gene SLC6A3 de réir Elsmarieke van de Giessen, Maartje M. L. de Win, Michael W.T. Tanck, Wim van den Brink, Frank Baas, Jan Booij
Foilsithe / Cruthaithe 2008Artigo -
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In Situ complement activation and T-cell immunity in leprosy spectrum: An immunohistological study on leprosy lesional skin de réir Nawal Bahia El Idrissi, Anand M. Iyer, Valeria Ramaglia, Patrícia Sammarco Rosa, Cléverson Teixeira Soares, Frank Baas, Pranab K. Das
Foilsithe / Cruthaithe 2017Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Medicine
Disease
Mutation
Pathology
Internal medicine
Neuroscience
Immunology
Molecular biology
Biochemistry
Cell biology
Amyotrophic lateral sclerosis
Chemistry
Immune system
Anatomy
Genotype
RNA
Exon
Phenotype
Endocrinology
Missense mutation
Allele
Complement system
Enzyme
Cancer research
Cerebellum
Dementia
Apoptosis