Oliver Brandau: search on Z-Library

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1

A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin-I

Oliver Brandau, Alfons Meindl, Reinhard Fässler, Attila Aszódi

Journal:

Developmental Dynamics

Year:

2001

Language:

english

File:

PDF, 1.32 MB

english, 2001

2

10.1038/2424

Coffey, Alison J., Brooksbank, Robert A., Brandau, Oliver, Oohashi, Toshitaka, Howell, Gareth R., Bye, Jacqueline M., Cahn, Anthony P., Durham, Jillian, Heath, Paul, Wray, Paul, Pavitt, Rebecca, Wilki

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 161 KB

english, 1998

3

10.1038/81627

Meindl, Alfons, Pusch, Carsten M., Zeitz, Christina, Brandau, Oliver, Pesch, Katrin, Achatz, Helene, Feil, Silke, Scharfe, Curt, Maurer, Johannes, Jacobi, Felix K., Pinckers, Alfred, Andreasson, Sten,

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 504 KB

english, 2000

4

UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2

Brandau, Oliver, Nyakatura, Gerald, Jedele, Kerry B, Platzer, Matthias, Achatz, Helene, Ross, Mark, Murken, Jan, Rosenthal, Andre, Meindl, Alfons

Journal:

European Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 369 KB

english, 1998

5

An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders

Dawn L. Thiselton, Jennifer McDowall, Oliver Brandau, Juliane Ramser, Fabiana d'Esposito, Shomi S. Bhattacharya, Mark T. Ross, Alison J. Hardcastle, Alfons Meindl

Journal:

Year:

2002

Language:

english

File:

PDF, 257 KB

english, 2002

6

An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders

Dawn L. Thiselton, Jennifer McDowall, Oliver Brandau, Juliane Ramser, Fabiana d'Esposito, Shomi S. Bhattacharya, Mark T. Ross, Alison J. Hardcastle, Alfons Meindl

Journal:

Year:

2002

Language:

english

File:

PDF, 39 KB

english, 2002

7

PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions☆

Attila Braun, Randi Bordoy, Fabio Stanchi, Markus Moser, G.ünter Kostka, Elisabeth Ehler, Oliver Brandau, Reinhard Fässler

Journal:

Experimental Cell Research

Year:

2003

Language:

english

File:

PDF, 1.11 MB

english, 2003

8

Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis

Attila Braun, Attila Aszódi, Heide Hellebrand, Alejandro Berna, Reinhard Fässler, Oliver Brandau

Journal:

Year:

2002

Language:

english

File:

PDF, 484 KB

english, 2002

9

Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice

Keiko Sakai, László Hiripi, Virpi Glumoff, Oliver Brandau, Riitta Eerola, Eero Vuorio, Zsuzsa Bösze, Reinhard Fässler, Attila Aszódi

Journal:

Year:

2001

Language:

english

File:

PDF, 2.45 MB

english, 2001

10

The murine Ten-m/Odz genes show distinct but overlapping expression patterns during development and in adult brain

Xiao-Hong Zhou, Oliver Brandau, Kang Feng, Toshitaka Oohashi, Yoshifumi Ninomiya, Uwe Rauch, Reinhard Fässler

Journal:

Gene Expression Patterns

Year:

2003

Language:

english

File:

PDF, 645 KB

english, 2003

11

Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction

Finsterer, Josef, Stöllberger, Claudia, Brandau, Oliver, Laccone, Franco, Bichler, Katharina, Laing, Nigel G

Journal:

International Journal of Cardiology

Year:

2014

Language:

english

File:

PDF, 186 KB

english, 2014

12

Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipation

Finsterer, Josef, Brandau, Oliver, Stöllberger, Claudia, Wallefeld, William, Laing, Nigel G., Laccone, Franco

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 361 KB

english, 2014

13

Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome

Steinkellner, Hannes, Etzler, Julia, Gogoll, Laura, Neesen, Jürgen, Stifter, Eva, Brandau, Oliver, Laccone, Franco

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.38 MB

english, 2014

14

X-linked Retinitis Pigmentosa: RPGR Mutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

Bader, Ingrid, Brandau, Oliver, Achatz, Helene, Apfelstedt-Sylla, Eckart, Hergersberg, Martin, Lorenz, Birgit, Wissinger, Bernd, Wittwer, Ba¨rbel, Rudolph, Gu¨nther, Meindl, Alfons, Meitinger, Thomas

Journal:

Investigative Ophthalmology & Visual Science

Year:

2003

Language:

english

File:

PDF, 306 KB

english, 2003

15

Amniotic fluid stem cells to study mTOR signaling in differentiation

Rosner, Margit, Schipany, Katharina, Shanmugasundaram, Bharanidharan, Lubec, Gert, Brandau, Oliver, Hengstschläger, Markus

Journal:

Year:

2012

Language:

english

File:

PDF, 877 KB

english, 2012

16

A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing

Bastaki, Fatma, Mohamed, Madiha, Nair, Pratibha, Saif, Fatima, Tawfiq, Nafisa, Al-Ali, Mahmoud Taleb, Brandau, Oliver, Hamzeh, Abdul Rezzak

Journal:

Molecular and Cellular Probes

Year:

2015

Language:

english

File:

PDF, 749 KB

english, 2015

17

Schmerzhafte Knoten

Valero, Teresa, Brandau, Oliver, Laccone, Franco, Radakovic, Sonja

Journal:

JDDG: Journal der Deutschen Dermatologischen Gesellschaft

Year:

2016

Language:

german

File:

PDF, 2.92 MB

german, 2016

18

Painful nodules

Valero, Teresa, Brandau, Oliver, Laccone, Franco, Radakovic, Sonja

Journal:

JDDG: Journal der Deutschen Dermatologischen Gesellschaft

Year:

2016

Language:

english

File:

PDF, 1.71 MB

english, 2016

19

Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome

Shukla, Anju, Hebbar, Malavika, Srivastava, Anshika, Kadavigere, Rajagopal, Upadhyai, Priyanka, Kanthi, Anil, Brandau, Oliver, Bielas, Stephanie, Girisha, Katta M

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 638 KB

english, 2017

20

C26-Ceramide as highly sensitive biomarker for the diagnosis of Farber Disease

Cozma, Claudia, Iurașcu, Marius-Ionuț, Eichler, Sabrina, Hovakimyan, Marina, Brandau, Oliver, Zielke, Susanne, Böttcher, Tobias, Giese, Anne-Katrin, Lukas, Jan, Rolfs, Arndt

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 2.60 MB

english, 2017

21

Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets

Francis, Fiona, Strom, Tim M., Hennig, Steffen, Böddrich, Annett, Lorenz, Bettina, Brandau, Oliver, Mohnike, Klaus L., Cagnoli, Michele, Steffens, Christina, Klages, Sven, Borzym, Katja, Pohl, Thomas,

Journal:

Genome Research

Year:

1997

Language:

english

File:

PDF, 590 KB

english, 1997

22

Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability

Bertoli-Avella, Aida M., Garcia-Aznar, Jose M., Brandau, Oliver, Al-Hakami, Fahad, Yüksel, Zafer, Marais, Anett, Grüning, Nana-Maria, Abbasi Moheb, Lia, Paknia, Omid, Alshaikh, Nahla, Alameer, Seham,

Journal:

European Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 954 KB

english, 2018

23

Clinical relevance and suppressive capacity of human MDSC subsets

Lang, Stephan, Bruderek, Kirsten, Kaspar, Cordelia, Höing, Benedikt, Kanaan, Oliver, Dominas, Nina, Hussain, Timon, Droege, Freya, Eyth, Christian Peter, Hadaschik, Boris, Brandau, Sven

Journal:

Clinical Cancer Research

Year:

2018

Language:

english

File:

PDF, 3.40 MB

english, 2018

24

Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report

Ratnasamy, Vithiya, Navaneethakrishnan, Suganthan, Sirisena, Nirmala Dushyanthi, Grüning, Nana-Maria, Brandau, Oliver, Thirunavukarasu, Kumanan, Dagnall, Casey L., McReynolds, Lisa J., Savage, Sharon

Journal:

BMC Medical Genetics

Year:

2018

Language:

english

File:

PDF, 890 KB

english, 2018

25

HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy—Report of 11 Patients

Kovacs-Nagy, Reka, Morin, Gilles, Nouri, Maria, Brandau, Oliver, Saadi, Nebal, Nouri, Mohammed, van den Broek, Florence, Prokisch, Holger, Mayr, Johannes, Wortmann, Saskia

Journal:

Neuropediatrics

Year:

2018

Language:

english

File:

PDF, 205 KB

english, 2018

26

Stromal versus tumoral inflammation differentially contribute to metastasis and poor survival in laryngeal squamous cell carcinoma

Höing, Benedikt, Kanaan, Oliver, Altenhoff, Petra, Petri, Robert, Thangavelu, Kruthika, Schlüter, Anke, Lang, Stephan, Bankfalvi, Agnes, Brandau, Sven

Journal:

Year:

2018

Language:

english

File:

PDF, 3.82 MB

english, 2018

27

Novel causative variants in patients with achromatopsia

Abdelkader, Ehab, Brandau, Oliver, Bergmann, Carsten, AlSalamah, Nuha, Nowilaty, Sawsan, Schatz, Patrik

Journal:

Ophthalmic Genetics

Year:

2018

Language:

english

File:

PDF, 1.38 MB

english, 2018

28

De novo mutation of emopamil binding protein ( EBP ) gene in a girl with Conradi-Hünermann-Happle syndrome

Soler-Cardona, Ana, Brandau, Oliver, Laccone, Franco, Tanew, Adrian, Radakovic, Sonja

Journal:

Clinical Case Reports

Year:

2019

Language:

english

File:

PDF, 504 KB

english, 2019

29

A novel POC1A variant in an alternatively spliced exon causes classic SOFT syndrome: clinical presentation of seven patients

Al-Kindi, Adila, Al-Shehhi, Maryam, Westenberger, Ana, Beetz, Christian, Scott, Patrick, Brandau, Oliver, Abbasi-Moheb, Lia, Yüksel, Zafer, Bauer, Peter, Rolfs, Arndt, Grüning, Nana-Maria

Journal:

Journal of Human Genetics

Year:

2019

File:

PDF, 791 KB

2019