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Showing 1–14 of 14 results

Advanced filters: Author: M Erdel Clear advanced filters

HP1 loses its chromatin clustering and phase separation function across evolution

Here, the authors compare HP1 from fission yeast, fly and mouse, and find that the propensity of HP1 to phase-separate and to cluster heterochromatin decrease in this order, suggesting an evolutionary adaptation of HP1 function.

Sanâa Bensaha
Dominika Lewandowska
Fabian Erdel
ResearchOpen Access10 Jul 2025
Nature Communications

Volume: 16, P: 1-15
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations

M Witsch-Baumgartner
E Ciara
G Utermann
Research12 Jan 2001
European Journal of Human Genetics

Volume: 9, P: 45-50
Immunochemical analysis of cathepsin B in lung tumours: an independent prognostic factor for squamous cell carcinoma patients

B Werle
H Lötterle
E Spiess
ResearchOpen Access10 Sept 1999
British Journal of Cancer

Volume: 81, P: 510-519
Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

Sander M Houten
Janet Koster
Hans R Waterham
Research20 Apr 2001
European Journal of Human Genetics

Volume: 9, P: 253-259
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Δ7-sterol reductase in Italy and report of three novel mutations

D De Brasi
T Esposito
G Andria
Research08 Dec 1999
European Journal of Human Genetics

Volume: 7, P: 937-940
Complete XY gonadal dysgenesis and aspects of the SRY genotype and gonadal tumor formation

S. Uehara
M. Hashiyada
K. Okamura
Research01 Jun 2002
Journal of Human Genetics

Volume: 47, P: 279-284
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

Andreas Janecke and colleagues identify mutations in MYO5B, encoding the type Vb myosin motor protein, in individuals with microvillus inclusion disease, implicating myosin Vb as a key regulator of epithelial cell polarity.

Thomas Müller
Michael W Hess
Andreas R Janecke
Research24 Aug 2008
Nature Genetics

Volume: 40, P: 1163-1165
Simple and reliably sensitive diagnosis and monitoring of Philadelphia chromosome-positive cells in chronic myeloid leukemia by interphase fluorescence in situ hybridization of peripheral blood cells

M Yanagi
K Shinjo
R Ohno
Research16 Apr 1999
Leukemia

Volume: 13, P: 542-552
Cysteine proteinase cathepsin H in tumours and sera of lung cancer patients: relation to prognosis and cigarette smoking

A Schweiger
A Staib
J Kos
ResearchOpen Access20 Jan 2000
British Journal of Cancer

Volume: 82, P: 782-788
Clinical applications of comparative genomic hybridization

Brynn Levy
Teresa M Dunn
Kurt Hirschhorn
Research01 Nov 1998
Genetics in Medicine

Volume: 1, P: 4-12
Cyclin E dysregulation and chromosomal instability in endometrial cancer

Michael M Hubalek
Andreas Widschwendter
Martin Widschwendter
Research29 Mar 2004
Oncogene

Volume: 23, P: 4187-4192
Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

Z Culig
J Hoffmann
H Klocker
ResearchOpen Access27 Aug 1999
British Journal of Cancer

Volume: 81, P: 242-251
Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancer

D Reimer
M Hubalek
A G Zeimet
Research25 Apr 2011
Oncogene

Volume: 30, P: 4038-4049
Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML?

G Webersinke
W Kranewitter
G Tschurtschenthaler
CorrespondenceOpen Access27 Jun 2014
Blood Cancer Journal

Volume: 4, P: e221

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HP1 loses its chromatin clustering and phase separation function across evolution

Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations

Immunochemical analysis of cathepsin B in lung tumours: an independent prognostic factor for squamous cell carcinoma patients

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Δ7-sterol reductase in Italy and report of three novel mutations

Complete XY gonadal dysgenesis and aspects of the SRY genotype and gonadal tumor formation

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

Simple and reliably sensitive diagnosis and monitoring of Philadelphia chromosome-positive cells in chronic myeloid leukemia by interphase fluorescence in situ hybridization of peripheral blood cells

Cysteine proteinase cathepsin H in tumours and sera of lung cancer patients: relation to prognosis and cigarette smoking

Clinical applications of comparative genomic hybridization

Cyclin E dysregulation and chromosomal instability in endometrial cancer

Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancer

Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML?

Search

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