Cargando…

The Characteristics of Human Genes: Analysis of Human Chromosome 22

Detalles Bibliográficos
Autores principales:	Dunham, Ian, Beare, David M., Collins, John E.
Formato:	Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2003
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447302/ https://www.ncbi.nlm.nih.gov/pubmed/18629020 http://dx.doi.org/10.1002/cfg.335

Ejemplares similares

Finishing the finished human chromosome 22 sequence
por: Cole, Charlotte G, et al.
Publicado: (2008)

Genome and gene alterations by insertions and deletions in the evolution of human and chimpanzee chromosome 22
por: Volfovsky, Natalia, et al.
Publicado: (2009)

DNA methylation profiling of human chromosomes 6, 20 and 22
por: Eckhardt, Florian, et al.
Publicado: (2006)

Functional Annotation of Proteome Encoded by Human Chromosome 22
por: Pinto, Sneha M., et al.
Publicado: (2014)

Human genes: Time to follow the roads less traveled?
por: Dunham, Ian
Publicado: (2018)

After 'completion': the changing face of human chromosomes 21 and 22
por: Taylor, Todd Duane
Publicado: (2004)

A genome annotation-driven approach to cloning the human ORFeome
por: Collins, John E, et al.
Publicado: (2004)

Comparative analysis of a BAC contig of porcine chromosome 13q31-q32 and human chromosome 3q21-q22
por: Van Poucke, Mario, et al.
Publicado: (2005)

The human homologue of unc-93 maps to chromosome 6q27 – characterisation and analysis in sporadic epithelial ovarian cancer
por: Liu, Ying, et al.
Publicado: (2002)

Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer.
por: Holmberg, E., et al.
Publicado: (1996)

A 4 Mb High Resolution BAC Contig on Bovine Chromosome 1q12 and Comparative Analysis With Human Chromosome 21q22
por: Drögemüller, Cord, et al.
Publicado: (2005)

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter–22q11.2
por: Hulsebos, T J M, et al.
Publicado: (1999)

The genomic structure of a human chromosome 22 nucleolar organizer region determined by TAR cloning
por: Kim, Jung-Hyun, et al.
Publicado: (2021)

Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5
por: Bajaj, Vineeta, et al.
Publicado: (2004)

Loss of heterozygosity on chromosome XP22.2-p22.13 and Xq26.1-q27.1 in human breast carcinomas.
por: Choi, C., et al.
Publicado: (1998)

Gene promoters show chromosome-specificity and reveal chromosome territories in humans
por: Gagniuc, Paul, et al.
Publicado: (2013)

Small supernumerary marker chromosomes derived from chromosome 14 and/or 22
por: Liehr, Thomas, et al.
Publicado: (2021)

Quantitative analysis of Y-Chromosome gene expression across 36 human tissues
por: Godfrey, Alexander K., et al.
Publicado: (2020)

Characteristics of hematologic malignancies with coexisting t(9;22) and inv(16) chromosomal abnormalities
por: Han, Eunhee, et al.
Publicado: (2014)

Genesis of Non-Coding RNA Genes in Human Chromosome 22—A Sequence Connection with Protein Genes Separated by Evolutionary Time
por: Delihas, Nicholas
Publicado: (2020)

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
por: Daelemans, Caroline, et al.
Publicado: (2010)

Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis.
por: Seitz, S., et al.
Publicado: (1997)

Cloning and Characterization of the Human USP22 Gene Promoter
por: Xiong, Jianjun, et al.
Publicado: (2012)

A Human Type 1 Diabetes Susceptibility Locus Maps to Chromosome 21q22.3
por: Concannon, Patrick, et al.
Publicado: (2008)

In Silico Analysis of Functional Single Nucleotide Polymorphisms in the Human TRIM22 Gene
por: Kelly, Jenna N., et al.
Publicado: (2014)

Y Chromosome Lineage- and Village-Specific Genes on Chromosomes 1p22 and 6q27 Control Visceral Leishmaniasis in Sudan
por: Miller, E. Nancy, et al.
Publicado: (2007)

A detailed physical map of a region within human chromosome 16q22.1
por: Frengen, E, et al.
Publicado: (2000)

Mutability and mutational spectrum of chromosome transmission fidelity genes
por: Stirling, Peter C., et al.
Publicado: (2011)

Deficit of Mitonuclear Genes on the Human X Chromosome Predates Sex Chromosome Formation
por: Dean, Rebecca, et al.
Publicado: (2015)

The Gene Guessing Game
por: Dunham, Ian
Publicado: (2000)

Contribution of Chromosome 9p21‐22 Deletion to the Progression of Human Renal Cell Carcinoma
por: Kinoshita, Hidefumi, et al.
Publicado: (1995)

A Worldwide Phylogeography for the Human X Chromosome
por: Santos-Lopes, Simone S., et al.
Publicado: (2007)

Gene Survival and Death on the Human Y Chromosome
por: Wilson Sayres, Melissa A., et al.
Publicado: (2013)

Roles of the Y chromosome genes in human cancers
por: Kido, Tatsuo, et al.
Publicado: (2015)

Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22
por: Beaney, Katherine E., et al.
Publicado: (2017)

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X
por: Leitão, Elsa, et al.
Publicado: (2022)

A scale invariant clustering of genes on human chromosome 7
por: Kendal, Wayne S
Publicado: (2004)

Chromosomal localization of putative tumor-suppressor genes in several human cancers.
por: Yokota, J, et al.
Publicado: (1991)

Future prospects for human genetics and genomics in drug discovery
por: Ghoussaini, Maya, et al.
Publicado: (2023)

Human immune interferon gene is located on chromosome 12
Publicado: (1983)

Cannot write session to /tmp/vufind_sessions/sess_b5c9qpt5pnlpfdi7cbrlpi6gag