Cargando…

Comparative analysis of vertebrate EIF2AK2 (PKR) genes and assignment of the equine gene to ECA15q24–q25 and the bovine gene to BTA11q12–q15

The structures of the canine, rabbit, bovine and equine EIF2AK2 genes were determined. Each of these genes has a 5' non-coding exon as well as 15 coding exons. All of the canine, bovine and equine EIF2AK2 introns have consensus donor and acceptor splice sites. In the equine EIF2AK2 gene, a uniq...

Descripción completa

Detalles Bibliográficos
Autores principales:	Perelygin, Andrey A, Lear, Teri L, Zharkikh, Andrey A, Brinton, Margo A
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2006
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689263/ https://www.ncbi.nlm.nih.gov/pubmed/16954046 http://dx.doi.org/10.1186/1297-9686-38-5-551

Ejemplares similares

Characterization of the equine 2'-5' oligoadenylate synthetase 1 (OAS1) and ribonuclease L (RNASEL) innate immunity genes
por: Rios, Jonathan J, et al.
Publicado: (2007)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

The working point $Q_{H}$ = 15.38, $Q_{V}$ = 15.42 and single bunch acceleration
por: Boussard, D, et al.
Publicado: (1978)

The psychiatric phenotype of 15q11.2-q13.3 duplications
por: Budisteanu, M., et al.
Publicado: (2021)

Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report
por: Rodrigues, Maurício A., et al.
Publicado: (2019)

Association study of 15q14 and 15q25 with high myopia in the Han Chinese population
por: Qiang, Yu, et al.
Publicado: (2014)

Incidence of the 15q+;17q- chromosome translocation in acute promyelocytic leukaemia (APL).
por: Sheer, D., et al.
Publicado: (1985)

Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus
por: Paparella, Annalisa, et al.
Publicado: (2023)

Abnormal sleep physiology in children with 15q11.2-13.1 duplication (Dup15q) syndrome
por: Saravanapandian, Vidya, et al.
Publicado: (2021)

A case of de novo duplication of 15q24-q26.3
por: Kim, Eun Young, et al.
Publicado: (2011)

A case of 15q11‐q13 duplication syndrome and literature review
por: Fu, Zhuo, et al.
Publicado: (2021)

Atypical 15q11.2-q13 Deletions and the Prader-Willi Phenotype
por: Grootjen, Lionne N., et al.
Publicado: (2022)

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
por: Battaglia, Agatino
Publicado: (2008)

Translocation (6;15)(q12;q15): A Novel Mutation in a Patient with Therapy-Related Myelodysplastic Syndrome
por: Ali, Saba F., et al.
Publicado: (2015)

A three‑way complex translocation of (15;15;17)(q24;q14;q21) involving two breakpoints on chromosome 15 in acute promyelocytic leukemia: A case report
por: Kim, Do-Hoon
Publicado: (2023)

Chromosome 15q24 microdeletion syndrome
por: Magoulas, Pilar L, et al.
Publicado: (2012)

The FES Gene at the 15q26 Coronary-Artery-Disease Locus Inhibits Atherosclerosis
por: Karamanavi, Elisavet, et al.
Publicado: (2022)

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder
por: Ouldim, Karim, et al.
Publicado: (2007)

High rates of de novo 15q11q13 inversions in human spermatozoa
por: Molina, Òscar, et al.
Publicado: (2012)

Minutes of the Q Q asymmetry meeting held on 15 11 90 and 20 11 90
por: Saint-Denis, R
Publicado: (1990)

Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication
por: Libotte, Francesco, et al.
Publicado: (2021)

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
por: Delorme, Richard, et al.
Publicado: (2010)

Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk
por: Baert-Desurmont, Stéphanie, et al.
Publicado: (2016)

Assignment of the Q-Bands of the Chlorophylls: Coherence Loss via Q(x) − Q(y) Mixing
por: Reimers, Jeffrey R., et al.
Publicado: (2013)

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
por: Wang, Linyan, et al.
Publicado: (2018)

Is the delta(980) a broad q$\overline{q}$q$\overline{q}$ state?
por: Bramon, A, et al.
Publicado: (1982)

Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures
por: Sutcliffe, James S, et al.
Publicado: (2003)

A rare case of acute promyelocytic leukemia with ider(17)(q10)t(15;17)(q22;q21) and favorable outcome
por: Liu, Yongming, et al.
Publicado: (2020)

Common variants at 2q37.3, 8q24.21, 15q21.3, and 16q24.1 influence chronic lymphocytic leukemia risk
por: Crowther-Swanepoel, Dalemari, et al.
Publicado: (2010)

Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report
por: Wafa, Abdulsamad, et al.
Publicado: (2016)

Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort
por: Simpson, Claire L., et al.
Publicado: (2013)

Partial trisomy of chromosome 15q and partial monopsony of 6q due to maternal balanced translocation
por: Singla, Shilpy, et al.
Publicado: (2014)

Molecular characterization of the t(4;12)(q27~28;q14~15) chromosomal rearrangement in lipoma
por: Agostini, Antonio, et al.
Publicado: (2016)

A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 Syndrome
por: Frohlich, Joel, et al.
Publicado: (2016)

A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication
por: Huang, Xiuzhu, et al.
Publicado: (2021)

Four-Heavy-Quark and Bound State Production in the $e^{+}e^{-} \to Q + \overline{Q}' + Q' + \overline{Q}$ and $e^{+}e^{-} \to (Q\overline{Q}') + Q' + \overline{Q}$ Processes in $Z^{0}$ Boson Pole
por: Kiselev, V V, et al.
Publicado: (1994)

Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancer
por: Loveday, Chey, et al.
Publicado: (2017)

Properties of beta oscillations in Dup15q syndrome
por: Saravanapandian, Vidya, et al.
Publicado: (2020)

Age of diagnosis for children with chromosome 15q syndromes
por: Wheeler, Anne C., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_encgl7iok6njmpjf6pq5qqt6bu