Chromosomes, Human, Pair 4
"Chromosomes, Human, Pair 4" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A specific pair of GROUP B CHROMOSOMES of the human chromosome classification.
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 4".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 4-5 [A11.284.187.520.300.280]
- Chromosomes, Human, Pair 4 [A11.284.187.520.300.280.285]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 4-5 [G05.360.162.520.300.280]
- Chromosomes, Human, Pair 4 [G05.360.162.520.300.280.285]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 4".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 4" by people in this website by year, and whether "Chromosomes, Human, Pair 4" was a major or minor topic of these publications.
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Below are the most recent publications written about "Chromosomes, Human, Pair 4" by people in Profiles.
Shoemaker MB, Bollmann A, Lubitz SA, Ueberham L, Saini H, Montgomery J, Edwards T, Yoneda Z, Sinner MF, Arya A, Sommer P, Delaney J, Goyal SK, Saavedra P, Kanagasundram A, Whalen SP, Roden DM, Hindricks G, Ellis CR, Ellinor PT, Darbar D, Husser D. Common genetic variants and response to atrial fibrillation ablation. Circ Arrhythm Electrophysiol. 2015 Apr; 8(2):296-302.
Husser D, Adams V, Piorkowski C, Hindricks G, Bollmann A. Chromosome 4q25 variants and atrial fibrillation recurrence after catheter ablation. J Am Coll Cardiol. 2010 Feb 23; 55(8):747-53.
Shields CL, Zahler J, Falk N, Furuta M, Eagle RC, Espinosa LE, Fischer PR, Shields JA. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child. Arch Ophthalmol. 2007 Jun; 125(6):840-2.
Safley AM, Sebastian S, Collins TS, Tirado CA, Stenzel TT, Gong JZ, Goodman BK. Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet-derived growth factor receptor-alpha genes in a patient with atypical chronic myeloid leukemia. Genes Chromosomes Cancer. 2004 May; 40(1):44-50.
Ramachandran B, Rappaport EF, Surrey S, Poncz M, Schwartz E. Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene. Nucleic Acids Res. 1990 Oct 11; 18(19):5919.
Guzzo C, Weiner M, Rappaport E, LaRocco P, Surrey S, Poncz M, Schwartz E. An Eco R1 polymorphism of a human platelet factor 4 (PF4) gene. Nucleic Acids Res. 1987 Jan 12; 15(1):380.