Hergersberg, M.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH

Blattner, Ariane, Brunner-Agten, Saskia, Ludin, Katja, Hergersberg, Martin, Herklotz, Roberto, Huber, Andreas R., Röthlisberger, Benno

Journal:

Blood Cells, Molecules, and Diseases

Year:

2013

Language:

english

File:

PDF, 1.33 MB

english, 2013

2

Corneal dystrophies and degenerations: a molecular genetics approach

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 38 KB

english, 2004

3

Seeing is believing: Applications for nanotechnology in medical imaging and drug discovery

Christoph Hergersberg, Nadeem Ishaque, Greg Chambers, Margaret Blohm

Journal:

NanoBioTechnology

Year:

2005

Language:

english

File:

PDF, 58 KB

english, 2005

4

Schizophrenia and smoking: Evidence for a common neurobiological basis?

Stassen, H.H., Bridler, R., H�gele, S., Hergersberg, M., Mehmann, B., Schinzel, A., Weisbrod, M., Scharfetter, C.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 89 KB

english, 2000

5

Haplotype Analysis in Determination of the Heredity of Erythropoietic Protoporphyria among Swiss Families

Hergersberg, Martin, Deybach, Jean-Charles, Schneider-Yin, Xiaoye, Rüfenacht, Urszula B., Schnyder, Cécile, Minder, Elisabeth I.

Journal:

The Journal of Investigative Dermatology

Year:

2001

Language:

english

File:

PDF, 160 KB

english, 2001

6

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype

M. Hergersberg, Jaya Balakrishnan, Thomas Bettecken, Francoise Chevalier-Porst, Christian Brägger, René Burger, Inge Einschenk, Sabina Liechti-Gallati, Michael Morris, Daniel Schorderet, Francine Thon

Journal:

Year:

1997

Language:

english

File:

PDF, 42 KB

english, 1997

7

Phenotypic variability of a distinct deletion in McLeod syndrome

Marcelo Miranda, Claudia Castiglioni, Beat M. Frey, Martin Hergersberg, Adrian Danek, Hans H. Jung

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 111 KB

english, 2007

8

Untersuchungen über den Verhornungsprozess in der Epidermis

Journal:

Cell and Tissue Research

Year:

1957

Language:

german

File:

PDF, 1.76 MB

german, 1957

9

Bilayer-penetrating properties enable apocytochrome c to follow a special import pathway into mitochondria

Wilco JORDI, Christoph HERGERSBERG, Ben de KRUIJFF

Journal:

Year:

1992

Language:

english

File:

PDF, 707 KB

english, 1992

10

Rapid Matrix-Assisted Refolding of Histidine-Tagged Proteins

Tetyana Dashivets, Nichole Wood, Christoph Hergersberg, Johannes Buchner, Martin Haslbeck

Journal:

Year:

2009

Language:

english

File:

PDF, 1.07 MB

english, 2009

11

Tissue-specific expression of a FMR1 /β-galactosidase fusion gene in transgenic mice

Hergersberg, Martin, Matsuo, Koichi, Gassmann, Max, Schaffner, Walter, Lüscher, Bernhard, Rülicke, Thomas, Aguzzi, Adriano

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 751 KB

english, 1995

12

Ancestral Founder of Mutation W283X in the Porphobilinogen Deaminase Gene among Acute Intermittent Porphyria Patients

Schneider-Yin, Xiaoye, Hergersberg, Martin, Goldgar, David E., Rüfenacht, Urszula B., Schuurmans, Macé M., Puy, Hervé, Deybach, Jean-Charles, Minder, Elisabeth I.

Journal:

Year:

2003

Language:

english

File:

PDF, 177 KB

english, 2003

13

Retinal detachment and cataract, facial dysmorphism, generalized osteoporosis, immobile spine and platyspondyly in a consanguinous kindred – a possible new syndrome

H Schmidt, G Rudolph, M Hergersberg, K Schneider, S Moradi, T Meitinger*

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 263 KB

english, 2001

14

Deletions in the spinal muscular atrophy gene region in a newborn with neuropathy and extreme generalized muscular weakness

Martin Hergersberg, Markus Glatzel, Andrea T. Capone, Sibylla Achermann, Alice Hagmann, Joachim Fischer, Jörg Ersch, Adriano Aguzzi, Eugen Boltshauser

Journal:

European Journal of Paediatric Neurology

Year:

2000

Language:

english

File:

PDF, 426 KB

english, 2000

15

Personalized medicine – seeing is believing

Hergersberg, Christoph

Journal:

Personalized Medicine

Year:

2006

Language:

english

File:

PDF, 76 KB

english, 2006

16

Genetische Analysen und Immunphänotypisierung in der Diagnostik hämatologischer Erkrankungen

Hergersberg,, Röthlisberger,, Heijnen,, Huber,

Journal:

Therapeutische Umschau

Year:

2004

File:

PDF, 251 KB

2004

17

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

18

McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement

Hans H. Jung, Martin Hergersberg, Marco Vogt, Jens Pahnke, Valerie Treyer, Benno Röthlisberger, Spyros S. Kollias, David Russo, Beat M. Frey

Journal:

Transfusion (Wiley)

Year:

2003

Language:

english

File:

PDF, 465 KB

english, 2003

19

PK Aarau: first homozygous nonsense mutation causing pyruvate kinase deficiency

Isabel Boo Sedano, Benno Röthlisberger, Guy Délèze, Cornelia Ottiger, Marc-Alain Panchard, André Spahr, Martin Hergersberg, Willi Bürgi, Andreas Huber

Journal:

British Journal of Haematology

Year:

2004

Language:

english

File:

PDF, 94 KB

english, 2004

20

The Long Form of CDK2 Arises via Alternative Splicing and Forms an Active Protein Kinase with Cyclins A and E

Ellenrieder, Claudia, Bartosch, Birke, Lee, Gladys Y.-C., Murphy, Martin, Sweeney, Claire, Hergersberg, Martin, Carrington, Mark, Jaussi, Rolf, Hunt, Tim

Journal:

DNA and Cell Biology

Year:

2001

Language:

english

File:

PDF, 418 KB

english, 2001

21

Molecular cloning and partial characterization of the gene for granule-bound starch synthase from a wildtype and an amylose-free potato (Solanum tuberosum L.)

R.G.F. Visser, M. Hergersberg, F.R. Van Der Leij, E. Jacobsen, B. Witholt, W.J. Feenstra

Journal:

Year:

1989

Language:

english

File:

PDF, 771 KB

english, 1989

22

Compound heterozygosity of Hb Hamilton and de novo mutated HbM Saskatoon

Saskia Brunner-Agten, Martin Hergersberg, Roberto Herklotz, Andreas Hirt, Andreas R. Huber

Journal:

Annals of Hematology

Year:

2010

Language:

english

File:

PDF, 65 KB

english, 2010

23

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

Wutz, Krisztina, Sauer, Christian, Zrenner, Eberhart, Lorenz, Birgit, Alitalo, Tiina, Broghammer, Martina, Hergersberg, Martin, Chapelle, Albert de La, Weber, Bernhard H F, Wissinger, Bernd

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 406 KB

english, 2002

24

Quantitative Monitoring of BCR – ABL Transcript – Suggestion of a Simplified Approach Considering Inaccuracy of Measurement and Calibration

Röthlisberger, Benno, Herklotz, Roberto, Hergersberg, Martin, Stricker, Christian, Bargetzi, Mario, Huber, Andreas R

Journal:

Leukemia and Lymphoma

Year:

2004

Language:

english

File:

PDF, 133 KB

english, 2004

25

Age at diagnosis and loss of heterozygosity on chromosome 1p and 19q in oligodendroglial tumors

M. Hergersberg, L. Mariani, E. Vassella, C. Murtin, J. Weis, M. Moschopulos, H. Laeng, H. Landolt, A. Huber, U. Roelcke

Journal:

Journal of Neuro-Oncology

Year:

2006

Language:

english

File:

PDF, 122 KB

english, 2006

26

The LTR promoter of the rat oncomodulin gene is regulated by cell-line specific accessibility in the LTR U3 region

Jürg M. Rentsch, Martin Hergersberg, Denis Banville, Martin W. Berchtold

Journal:

Archives of Biochemistry and Biophysics

Year:

2006

Language:

english

File:

PDF, 706 KB

english, 2006

27

Spondylo-ocular syndrome: a new entity with crystalline lens malformation, cataract, retinal detachment, osteoporosis, and platyspondyly

Gunther Rudolph, Petros Kalpadakis, Thomas Bettecken, Peter Lichtner, Christos Haritoglou, Martin Hergersberg, Thomas Meitinger, Heinrich Schmidt

Journal:

American Journal of Ophthalmology

Year:

2003

Language:

english

File:

PDF, 349 KB

english, 2003

28

A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms

Alessandra Baumer, Ute Wiedemann, Martin Hergersberg, Albert Schinzel

Journal:

Year:

2001

Language:

english

File:

PDF, 295 KB

english, 2001

29

Stabilization of Proteins and Peptides in Diagnostic Immunological Assays by the Molecular Chaperone Hsp25

Monika Ehrnsperger, Christoph Hergersberg, Ulla Wienhues, Alfons Nichtl, Johannes Buchner

Journal:

Analytical Biochemistry

Year:

1998

Language:

english

File:

PDF, 247 KB

english, 1998

30

Biological aspects of cytosine methylation in eukaryotic cells

Journal:

Cellular and Molecular Life Sciences

Year:

1991

Language:

english

File:

PDF, 1.75 MB

english, 1991

31

Expression in mammalian cells of a cloned gene encoding murine DNA methyltransferase

Czank, Andreas, Häuselmann, Remo, Page, Andrea W., Leonhardt, Heinrich, Bestor, Timothy H., Schaffner, Walter, Hergersberg, Martin

Journal:

Year:

1991

Language:

english

File:

PDF, 930 KB

english, 1991

32

Epidermodysplasia Verruciformis in a HIV-Positive Patient Homozygous for the c917A→T Polymorphism in the TMC8/EVER2 Gene

Hohenstein, E., Rady, P.L., Hergersberg, M., Huber, A.R., Tyring, S.K., Bregenzer, T., Streit, M., Itin, P.

Journal:

Year:

2009

Language:

english

File:

PDF, 185 KB

english, 2009

33

Mcleod syndrome: A novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings

Hans H. Jung, Martin Hergersberg, Stefan Kneifel, Hatem Alkadhi, Regula Schiess, Maike Weigell-Weber, Geoff Daniels, Spyros Kollias, Klaus Hess

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 1.19 MB

english, 2001

34

260 Mutation complexe du gène Peripherin/RDS dans une famille avec retinal pattern dystrophy

Pajic, B., Weigell-Weber, M., Schipper, I., Kryenbühl, C.H., Buechi, E., Hergersberg, M., Spiegel, R.

Journal:

Journal Français d'Ophtalmologie

Year:

2005

Language:

english

File:

PDF, 1007 KB

english, 2005

35

A fascinating overview of the biology of fragile X syndrome

Hergersberg, Martin

Journal:

European Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 235 KB

english, 2018

36

High throughput functional genomics: Identification of novel genes with tumor suppressor phenotypes

Kerstin Koenig-Hoffmann, Angelika L. Bonin-Debs, Irene Boche, Beate Gawin, Andrea Gnirke, Christoph Hergersberg, Frank Madeo, Michael Kazinski, Matthias Klein, Christian Korherr, Dieter Link, Sascha R

Journal:

International Journal of Cancer

Year:

2005

Language:

english

File:

PDF, 244 KB

english, 2005

37

Contact sites between inner and outer membranes: Structure and role in protein translocation into the mitochondria

Nikolaus Pfanner, Joachim Rassow, Ulla Wienhues, Christoph Hergersberg, Thomas Söllner, Karin Becker, Walter Neupert

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

1990

Language:

english

File:

PDF, 329 KB

english, 1990

38

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Kotzot, Dieter, Schmitt, Silke, Bernasconi, Fabiana, Robinson, Wendy P., Lurie, Iosif W., Ilyina, Helena, Méhes, Károly, Hamel, Ben C.J., Otten, Barto J., Hergersberg, Martin, Werder, Edmond, Schoenle

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 2.19 MB

english, 1995

39

A NOVEL COMPLEX MUTATION EVENT IN THE PERIPHERIN/RDS GENE IN A FAMILY WITH RETINAL PATTERN DYSTROPHY

PAJIC, BOJAN, WEIGELL-WEBER, MAIKE, SCHIPPER, ISAAK, KRYENBüHL, CHRISTOPH, BüCHI, ERNST R., SPIEGEL, ROLAND, HERGERSBERG, MARTIN

Journal:

Year:

2006

Language:

english

File:

PDF, 1.14 MB

english, 2006

40

Schizophrenia and smoking: Evidence for a common neurobiological basis?

Stassen, H.H., Bridler, R., Hägele, S., Hergersberg, M., Mehmann, B., Schinzel, A., Weisbrod, M., Scharfetter, C.

Journal:

American Journal of Medical Genetics

Year:

2000

File:

PDF, 101 KB

2000

41

Schizophrenia and smoking: Evidence for a common neurobiological basis?

Stassen, H.H., Bridler, R., Hägele, S., Hergersberg, M., Mehmann, B., Schinzel, A., Weisbrod, M., Scharfetter, C.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 101 KB

english, 2000

42

Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product

Dirk Schindelhauer, Michael Weiss, Heide Hellebrand, Astrid Golla, Martin Hergersberg, Reinhard Seger, B. H. Belohradsky, A. Meindl

Journal:

Year:

1996

Language:

english

File:

PDF, 210 KB

english, 1996

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски