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Karpas 422 (DSMZ) | Bioz | Ratings For Life-Science Research
Karpas 422 (DSMZ) | Bioz | Ratings For Life-Science Research

Focal chromosomal copy number aberrations in cancer—Needles in a genome  haystack - ScienceDirect
Focal chromosomal copy number aberrations in cancer—Needles in a genome haystack - ScienceDirect

Focal chromosomal copy number aberrations in cancer—Needles in a genome  haystack - ScienceDirect
Focal chromosomal copy number aberrations in cancer—Needles in a genome haystack - ScienceDirect

Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative  Potential | Science
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential | Science

Cancers | Free Full-Text | The Effect of Atm Loss on Radiosensitivity of a  Primary Mouse Model of Pten-Deleted Brainstem Glioma
Cancers | Free Full-Text | The Effect of Atm Loss on Radiosensitivity of a Primary Mouse Model of Pten-Deleted Brainstem Glioma

Overview of all mutations, focal deletions, 6q deletions, and TCR... |  Download Scientific Diagram
Overview of all mutations, focal deletions, 6q deletions, and TCR... | Download Scientific Diagram

Six-gene signature for predicting survival in patients with head and neck  squamous cell carcinoma | Aging
Six-gene signature for predicting survival in patients with head and neck squamous cell carcinoma | Aging

Genome-wide somatic copy number alteration analysis and database  construction for cervical cancer | SpringerLink
Genome-wide somatic copy number alteration analysis and database construction for cervical cancer | SpringerLink

Clinical Cancer Research on Twitter: "Kline et al report on the results of  PNOC003, a multi-center precision medicine trial for children and young  adults with newly diagnosed diffuse intrinsic pontine glioma.  https://t.co/MVhK6LA5fe #
Clinical Cancer Research on Twitter: "Kline et al report on the results of PNOC003, a multi-center precision medicine trial for children and young adults with newly diagnosed diffuse intrinsic pontine glioma. https://t.co/MVhK6LA5fe #

Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia |  Haematologica
Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia | Haematologica

The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute  lymphoblastic leukemia but is not associated with outcome. A report on  behalf of the GIMEMA Acute Leukemia Working Party | Haematologica
The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. A report on behalf of the GIMEMA Acute Leukemia Working Party | Haematologica

JCI Insight - Focal adhesion proteins Pinch1 and Pinch2 regulate bone  homeostasis in mice
JCI Insight - Focal adhesion proteins Pinch1 and Pinch2 regulate bone homeostasis in mice

Frontiers | Somatic Copy Number Alterations in Human Cancers: An Analysis  of Publicly Available Data From The Cancer Genome Atlas
Frontiers | Somatic Copy Number Alterations in Human Cancers: An Analysis of Publicly Available Data From The Cancer Genome Atlas

Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE
Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE

Histopathologic subtype-specific genomic profiles of renal cell carcinomas  identified by high-resolution whole-genome single nucleotide polymorphism  array analysis
Histopathologic subtype-specific genomic profiles of renal cell carcinomas identified by high-resolution whole-genome single nucleotide polymorphism array analysis

Figures and data in The novel lncRNA lnc-NR2F1 is pro-neurogenic and  mutated in human neurodevelopmental disorders | eLife
Figures and data in The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders | eLife

Pan-cancer analysis of homozygous deletions in primary tumours uncovers  rare tumour suppressors | Nature Communications
Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors | Nature Communications

Cumulative haploinsufficiency and triplosensitivity drive aneuploidy  patterns and shape the cancer genome. - Abstract - Europe PMC
Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome. - Abstract - Europe PMC

T-Cell Acute Lymphoblastic Leukemia | Encyclopedia MDPI
T-Cell Acute Lymphoblastic Leukemia | Encyclopedia MDPI

The focal deletion of chr6p21.32 encompassing HLA class II alleles. a... |  Download Scientific Diagram
The focal deletion of chr6p21.32 encompassing HLA class II alleles. a... | Download Scientific Diagram

Specific deletion of focal adhesion kinase suppresses tumor formation and  blocks malignant progression
Specific deletion of focal adhesion kinase suppresses tumor formation and blocks malignant progression

WWOX, the FRA16D gene: A target of and a contributor to genomic instability  - Hussain - 2019 - Genes, Chromosomes and Cancer - Wiley Online Library
WWOX, the FRA16D gene: A target of and a contributor to genomic instability - Hussain - 2019 - Genes, Chromosomes and Cancer - Wiley Online Library

Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative  Potential | Science
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential | Science

Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE
Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE

The Importance of Detecting Copy Number Variants (CNVs) in the Cancer Genome
The Importance of Detecting Copy Number Variants (CNVs) in the Cancer Genome

Sites in the genome of frequent cancer focal deletions. (A) Average DNA...  | Download Scientific Diagram
Sites in the genome of frequent cancer focal deletions. (A) Average DNA... | Download Scientific Diagram

Symmetry | Free Full-Text | Machine Learning Reveals Molecular Similarity  and Fingerprints in Structural Aberrations of Somatic Cancer
Symmetry | Free Full-Text | Machine Learning Reveals Molecular Similarity and Fingerprints in Structural Aberrations of Somatic Cancer

Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to  Cause Hypergonadotropic Hypogonadism in Men
Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men