Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization.
MR Speicher, B Schoell, S du Manoir… - The American journal …, 1994 - ncbi.nlm.nih.gov
We analyzed 19 chromophobe renal cell carcinomas by means of comparative genomic
hybridization. Two tumors revealed no numerical abnormalities. In the remaining 17 cases we …
hybridization. Two tumors revealed no numerical abnormalities. In the remaining 17 cases we …
Autophagic cell death restricts chromosomal instability during replicative crisis
J Nassour, R Radford, A Correia, JM Fusté, B Schoell… - Nature, 2019 - nature.com
Replicative crisis is a senescence-independent process that acts as a final barrier against
oncogenic transformation by eliminating pre-cancerous cells with disrupted cell cycle …
oncogenic transformation by eliminating pre-cancerous cells with disrupted cell cycle …
[PDF][PDF] Defined conditions for the isolation and expansion of basal prostate progenitor cells of mouse and human origin
…, SM Goeppinger, A Jauch, B Schoell… - Stem cell reports, 2015 - cell.com
Methods to isolate and culture primary prostate epithelial stem/progenitor cells (PESCs)
have proven difficult and ineffective. Here, we present a method to grow and expand both …
have proven difficult and ineffective. Here, we present a method to grow and expand both …
Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization
…, A Jauch, C Cybulski, B Schoell… - … journal of cancer, 2005 - Wiley Online Library
Very little is known about the chromosomal regions harbouring genes involved in initiation
and progression of BRCAX‐associated breast cancers. We applied comparative genomic …
and progression of BRCAX‐associated breast cancers. We applied comparative genomic …
Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH …
…, M Granzow, M Keller, H Holtgreve-Grez, B Schoell… - Human genetics, 2002 - Springer
Cryptic subtelomeric chromosome rearrangements are a major cause of mild to severe
mental retardation pointing out the necessity of sensitive screening techniques to detect such …
mental retardation pointing out the necessity of sensitive screening techniques to detect such …
Multicolor karyotype analyses of mouse embryonic stem cells
J Guo, A Jauch, H Holtgreve-Grez, B Schoell… - In Vitro Cellular & …, 2005 - Springer
The manipulation of embryonic stem (ES) cells to introduce directional genetic changes into
the genome of mice has become an important tool in biomedical research. Monitoring of cell …
the genome of mice has become an important tool in biomedical research. Monitoring of cell …
Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics
M Granzow, S Popp, S Weber, B Schoell… - Cancer genetics and …, 2001 - Elsevier
Data concerning cytogenetic features of childhood ependymoma are rare. In this article, a
gain of 1q was identified as the sole alteration in a primary childhood infratentorial …
gain of 1q was identified as the sole alteration in a primary childhood infratentorial …
High resistance to X-rays and therapeutic carbon ions in glioblastoma cells bearing dysfunctional ATM associates with intrinsic chromosomal instability
I Dokic, A Mairani, S Brons, B Schoell… - … journal of radiation …, 2015 - Taylor & Francis
Purpose: To investigate chromosomal instability and radiation response mechanisms in
glioblastoma cells. Methods and materials: We undertook a comparative analysis of two patient-…
glioblastoma cells. Methods and materials: We undertook a comparative analysis of two patient-…
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der (5) t (3; 5)(q27; p15. 3) in a family with three mentally retarded individuals
…, M Keller, H Holtgreve-Grez, M Brough, B Schoell… - Human genetics, 2000 - Springer
Cryptic rearrangements involving the terminal regions of chromosomes are suspected to be
the cause of idiopathic mental retardation in a significant number of cases. This finding …
the cause of idiopathic mental retardation in a significant number of cases. This finding …
Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis
I Scholz, S Popp, M Granzow, B Schoell… - Cancer genetics and …, 2001 - Elsevier
We used comparative genomic hybridization (CGH) to study DNA copy number changes in
71 children with acute lymphoblastic leukemia (ALL) including 50 B-lineage and 21 T-ALLs. …
71 children with acute lymphoblastic leukemia (ALL) including 50 B-lineage and 21 T-ALLs. …