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Chromosome 10
Construction of Stable Mouse Arti Cial Chromosome from Native Mouse
134 Mb (Almost the Same As the Size of Chromosome 10). It Is ~4–4.5% of the Total Human Genome
WNT16 Is a New Marker of Senescence
Gene Mapping of Familial Autosomal Dominant Dilated Cardiomyopathy to Chromosome 10Q21-23
Chromosome 10
Chromosome 10 Introduction the Genetic Length of Chromosome 10 Is ~135 Mb. It Is ~4–4.5% of the Whole Human Genome. the Long A
Partial Monosomy of Chromosome 10 Short Arms
Chromosome 10 Abnormality Predicts Prognosis of Neuroblastoma Patients with Bone Marrow Metastasis
Terminal Deletion of the Long Arm of Chromosome 10 on September 30, 2021 by Guest
Chicken Skeletal Muscle-Associated Macroarray for Gene Discovery
Duplications of 10Q FTNW
Supplementary Table 3. Genes Specifically Regulated by Zol (Non-Significant for Fluva)
The Variants of Maize Chromosome 10 and Their Roles in Meiotic Drive
Novel and Highly Recurrent Chromosomal Alterations in Se´Zary Syndrome
Molecular Cytogenetic Analysis of 10;11 Rearrangements in Acute
Frequent Somatic Transfer of Mitochondrial DNA Into the Nuclear Genome of Human Cancer Cells
Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
Centromere Deletion in Cryptococcus Deuterogattii Leads to Neocentromere Formation and Chromosome Fusions Klaas Schotanus, Joseph Heitman*
Top View
TWNK Gene Twinkle Mtdna Helicase
Transcriptome Characterization of Human Mammary Cell Lines Expressing Different Levels of ERBB2 by Serial Analysis of Gene Expression
Mouse Chromosome 10
Supporting Information SI Materials and Methods Mice And
Allele Loss on Chromosome 10 and Point Mutation of Ras Oncogenes Are Infrequent in Tumors of MEN 2 A
Diversity and Abundance of the Abnormal Chromosome 10 Meiotic Drive Complex in Zea Mays
Construction of Neocentromere-Based Human Minichromosomes for Gene Delivery and Centromere Studies
10Q25 and 10Q26 Deletions
Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
Loss of Heterozygosity on Chromosome 10 Is More Extensive in Primary (De Novo) Than in Secondary Glioblastomas Hironori Fujisawa, Rui M
Chromosome 10 Abnormality Predicts Prognosis of Neuroblastoma
Integrity of the Human Centromere DNA Repeats Is Protected by CENP-A, CENP-C, and CENP-T
Analysis of the Functional Role of Chromosome 10 Loss in Human Glioblastomas1
Familial Pericentric Inversion (10) and Its Effect on Two Offspring
Centromere Retention and Loss During the Descent of Maize from a Tetraploid Ancestor
Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate Genes
10P Proximal Deletions Rescue FTNW
Duplications of 10P FTNW
Chromosome 10Q Deletion Del (10)(Q26.1Q26.3) Is Associated with Cataract
Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase ␥
REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
Download.Soe.Ucsc.Edu/Goldenpath/Mm10/Database/Refflat.Txt.Gz, Accessed 21 November 2019)
(12) Patent Application Publication (10) Pub. No.: US 2012/0053062 A1 BROOKS (43) Pub