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1

Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism

Schiaffino, M.Vittoria, Bassi, Maria T., Galli, Lucia, Renieri, Alessandra, Bruttini, Mirella, Nigris, Filomena De, Bergen, Arthur A.B., Charles, Stephen J., Yates, John R.W., Meindl, Alfons, Lewis, R

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 3.94 MB

english, 1995

2

Fishing is not wrestling: Neural underpinnings of the verb instrumentality effect

Malyutina, Svetlana, Dragoy, Olga, Ivanova, Maria, Laurinavichyute, Anna, Petrushevsky, Alexey, Meindl, Thomas, Pöppel, Ernst, Gutyrchik, Evgeny

Journal:

Journal of Neurolinguistics

Year:

2016

Language:

english

File:

PDF, 616 KB

english, 2016

3

Network-specific resting-state connectivity changes in the premotor-parietal axis in writer's cramp

Mantel, Tobias, Meindl, Tobias, Li, Yong, Jochim, Angela, Gora-Stahlberg, Gina, Kräenbring, Jona, Berndt, Maria, Dresel, Christian, Haslinger, Bernhard

Journal:

NeuroImage: Clinical

Year:

2018

Language:

english

File:

PDF, 468 KB

english, 2018

4

Cell wall composition of chlorococcal algae

Maria Blumreisinger, Doris Meindl, Eckhard Loos

Journal:

Year:

1983

Language:

english

File:

PDF, 185 KB

english, 1983

5

Variation in mammalian proximal femoral development: comparative analysis of two distinct ossification patterns

Maria A. Serrat, Philip L. Reno, Melanie A. McCollum, Richard S. Meindl, C. Owen Lovejoy

Journal:

Journal of Anatomy

Year:

2007

Language:

english

File:

PDF, 252 KB

english, 2007

6

10.1038/78182

Wright, Alan F., Vervoort, Raf, Lennon, Alan, Bird, Alan C., Tulloch, Brian, Axton, Richard, Miano, Maria G., Meindl, Alfons, Meitinger, Thomas, Ciccodicola, Alfredo

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 1.62 MB

english, 2000

7

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation

Martínez-Garay, Isabel, Tomás, Miguel, Oltra, Silvestre, Ramser, Juliane, Moltó, Maria D, Prieto, Félix, Meindl, Alfons, Kutsche, Kerstin, Martínez, Francisco

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 162 KB

english, 2006

8

Reaction of monocytes to polystyrene and silica nanoparticles in short-term and long-term exposures

Mrakovcic, Maria, Meindl, Claudia, Roblegg, Eva, Fröhlich, Eleonore

Journal:

Toxicology Research

Year:

2014

Language:

english

File:

PDF, 3.23 MB

english, 2014

9

Methylphenidate Effects on Brain Activity as a Function of SLC6A3 Genotype and Striatal Dopamine Transporter Availability

Kasparbauer, Anna-Maria, Rujescu, Dan, Riedel, Michael, Pogarell, Oliver, Costa, Anna, Meindl, Thomas, la Fougère, Christian, Ettinger, Ulrich

Journal:

Neuropsychopharmacology

Year:

2015

Language:

english

File:

PDF, 1.61 MB

english, 2015

10

Development of a new LAMP assay for the detection of CSFV strains from Cuba: a proof-of-concept study

Postel, Alexander, Pérez, Lester J., Perera, Carmen L., Schmeiser, Stefanie, Meyer, Denise, Meindl-Boehmer, Alexandra, Rios, Liliam, Austermann-Busch, Sophia, Frias-Lepoureau, Maria T., Becher, Paul

Journal:

Archives of Virology

Year:

2015

Language:

english

File:

PDF, 478 KB

english, 2015

11

Examining the teaching roles and experiences of non-physician health care providers in family medicine education: a qualitative study

Beber, Serena, Antao, Viola, Telner, Deanna, Krueger, Paul, Peranson, Judith, Meaney, Christopher, Meindl, Maria, Webster, Fiona

Journal:

BMC Medical Education

Year:

2015

Language:

english

File:

PDF, 356 KB

english, 2015

12

Association of COMT and SLC6A3 polymorphisms with impulsivity, response inhibition and brain function

Kasparbauer, Anna-Maria, Merten, Natascha, Aichert, Désirée S., Wöstmann, Nicola, Meindl, Thomas, Rujescu, Dan, Ettinger, Ulrich

Journal:

Year:

2015

Language:

english

File:

PDF, 682 KB

english, 2015

13

The Genotype of the Original Wiskott Phenotype

Binder, Vera, Albert, Michael H., Kabus, Maria, Bertone, Marko, Meindl, Alfons, Belohradsky, Bernd H.

Journal:

Boston Medical and Surgical Journal

Year:

2006

Language:

english

File:

PDF, 328 KB

english, 2006

14

A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

Meindl, Alfons, Carvalho, Maria Raquel S., Herrmann, Klaus, Lorenz, Bettina, Achatz, Helene, Lorenz, Birgit, Apfelstedt-Sylla, Eckart, Wittwer, Bärbel, Ross, Mark, Meitinger, Thomas

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 6.28 MB

english, 1995

15

Decreased GLUT1/NHE1 RNA expression in whole blood predicts disease severity in patients with COVIDâ19

Mustroph, Julian, Hupf, Julian, Hanses, Frank, Evert, Katja, Baier, Maria J., Evert, Matthias, Meindl, Christine, Wagner, Stefan, Hubauer, Ute, Pietrzyk, Gabriela, Leininger, Simon, Staudner, Stephan,

Journal:

ESC Heart Failure

Year:

2020

File:

PDF, 511 KB

2020