Results 51 to 60 of about 3,740,880 (323)

An improved Plasmodium cynomolgi genome assembly reveals an unexpected methyltransferase gene expansion. [PDF]

open access: yes, 2017
Background: Plasmodium cynomolgi, a non-human primate malaria parasite species, has been an important model parasite since its discovery in 1907. Similarities in the biology of P.
Berriman, Matt   +7 more
core   +2 more sources

Evolutionary dynamics of olfactory receptor genes in chordates: interaction between environments and genomic contents

open access: yesHuman Genomics, 2009
Olfaction is essential for the survival of animals. Versatile odour molecules in the environment are received by olfactory receptors (ORs), which form the largest multigene family in vertebrates. Identification of the entire repertories of OR genes using
Niimura Yoshihito
doaj   +1 more source

Accessing the Variability of Multicopy Genes in Complex Genomes using Unassembled Next-Generation Sequencing Reads: The Case of Trypanosoma cruzi Multigene Families

open access: yesmBio, 2022
Repetitive elements cause assembly fragmentation in complex eukaryotic genomes, limiting the study of their variability. The genome of Trypanosoma cruzi, the parasite that causes Chagas disease, has a high repetitive content, including multigene families.
João Luís Reis-Cunha   +15 more
doaj   +1 more source

Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands.

open access: yesProceedings of the National Academy of Sciences of the United States of America, 1999
Two related integral membrane proteins, claudin-1 and -2, recently were identified as novel components of tight junction (TJ) strands. Here, we report six more claudin-like proteins, indicating the existence of a claudin gene family.
K. Morita   +3 more
semanticscholar   +1 more source

DIFFERENTIATION OF A MULTIGENE FAMILY BETWEEN POPULATIONS [PDF]

open access: yesEvolution, 1987
Differentiation of a multigene family between populations is investigated under the forces of intrachromosomal unbiased gene conversion, neutral mutation, recombination, and random drift. The infinite-site model without recombination within the gene is employed, and the average numbers of the different sites between pairs of genes at the same locus and
openaire   +3 more sources

RBCS1A and RBCS3B, two major members within the Arabidopsis RBCS multigene family, function to yield sufficient Rubisco content for leaf photosynthetic capacity

open access: yesJournal of Experimental Botany, 2012
Ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) small subunit (RBCS) is encoded by a nuclear RBCS multigene family in many plant species.
M. Izumi   +4 more
semanticscholar   +1 more source

Expression of genes related to flavonoid and stilbene synthesis as affected by signaling chemicals and Botrytis cinerea in grapevines

open access: yesBiologia Plantarum, 2014
Recent studies have shown that the expression of genes related to the synthesis of flavonoids, such as the phenylalanineammonia lyase (PAL), chalcone synthase (CHS), chalcone isomerase (CHI), and stilbene synthase (STS) genes were induced in response to ...
S. Y. Ahn   +3 more
doaj   +1 more source

Quadruple context-free L-System mathematical tools as origin of biological evolution [PDF]

open access: yes, 2010
It is well known that A, T, G, C annealed together early in evolution and the long stretch of DNA was found which ultimately resulted into chromosomes of different organisms.
Arunava Goswami   +4 more
core   +2 more sources

Effect of individual suppression of RBCS multigene family on Rubisco contents in rice leaves.

open access: yesPlant, Cell and Environment, 2012
In higher plants, a small subunit of Rubisco is encoded for by an RBCS multigene family in the nuclear genome. However, it is unknown how each multigene member contributes to the accumulation of Rubisco holoenzyme.
Shun Ogawa   +4 more
semanticscholar   +1 more source

First identified Korean family with Tatton-Brown-Rahman Syndrome caused by the novel variant c.118G>C p.(Glu40Gln) [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2019
Tatton-Brown-Rahman Syndrome (TBRS), an overgrowth syndrome caused by heterozygous mutation of DNMT3A, first was described in 2014. Approximately 60 DNMT3A variants, including 32 missense variants, have been reported, with most missense mutations located
Cha Gon Lee, Ja-Hyun Jang, Ji-Young Seo
doaj   +1 more source

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