听力与言语-语言病理学

行为科学

医学伦理学

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  • Signatures of positive selection on the hepatic lipase gene in human populations.

    abstract::The hepatic lipase plays a central role in the lipid metabolism, catalyzing the hydrolysis of phospholipids, monoglycerides, diglycerides, and triglycerides, and acyl-CoA. It is also implied in the conversion of very low-density lipoprotein and intermediate density lipoprotein to low density lipoproteins. As a consequ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Flores SV,Olivari CF,Prado LF

    更新日期:2020-03-01 00:00:00

  • Mining genes associated with furanocoumarin biosynthesis in an endangered medicinal plant, Glehnia littoralis.

    abstract::The endangered medicinal plant Glehnia littoralis is one of the important natural source of furanocoumarin, which has been used as mucolytic, antitussive, antitumour and antibacterial. However, the genetic information of furanocoumarin biosynthesis in G. littoralis is scarce at present. The objective of this study was...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Song J,Luo H,Xu Z,Zhang Y,Xin H,Zhu D,Zhu X,Liu M,Wang W,Ren H,Chen H,Gao T

    更新日期:2020-01-01 00:00:00

  • Identification of QTLs in oil palm (Elaeis guineensis Jacq.) using SSR markers through association mapping.

    abstract::Oil palm (Elaeis guineensis Jacq.) is a perennial vegetable and a high oil-yielding crop (4-6 t/ha). There is a large scope for increasing the oil yield by selecting elite planting material for breeding programme in germplasm evaluation, characterization and utilization. In the present study, a diverse range of 150 oi...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Bhagya HP,Kalyana Babu B,Gangadharappa PM,Naika MBN,Satish D,Mathur RK

    更新日期:2020-01-01 00:00:00

  • Psychiatric features and variable neurodevelopment outcome in four females with IQSEC2 spectrum disorder.

    abstract::IQSEC2 is an X-linked gene highly expressed at the excitatory synapses where it plays a crucial role in α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking and synaptic plasticity. To date, several males and females with severe to profound intellectual disability have been reported harbouring fra...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Accogli A,Eric Jarvis G,Schiavetto A,Lai L,Amirali EL,Jimenez Cruz DA,Rivière JB,Trakadis Y

    更新日期:2020-01-01 00:00:00

  • Identification of anthocyanin biosynthesis related microRNAs and total microRNAs in Lonicera edulis by high-throughput sequencing.

    abstract::miRNAs are important regulators of plant gene expression. There are few studies on the regulation of miRNAs in Lonicera edulis. We used high-throughput sequencing technology to analyse miRNAs in L. edulis, aiming to identify miRNAs and elucidate their function in L. edulis. In the present study, we employed the high-t...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Cui J,Gao Z,Li B,Li J,Li X,Wang C,Cheng D,Dai C

    更新日期:2020-01-01 00:00:00

  • The use of a genetic relationship matrix biases the best linear unbiased prediction.

    abstract::The best linear unbiased prediction (BLUP), derived from the linear mixed model (LMM), has been popularly used to estimate animal and plant breeding values (BVs) for a few decades. Conventional BLUP has a constraint that BVs are estimated from the assumed covariance among unknown BVs, namely conventional BLUP assumes ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Kim B

    更新日期:2020-01-01 00:00:00

  • Characterization of bZIP transcription factors from Dimocarpus longan Lour. and analysis of their tissue-specific expression patterns and response to heat stress.

    abstract::Members of the bZIP transcription factor family play crucial roles in the regulation of plant development, biosynthesis of secondary metabolites, and response to abiotic and biotic stresses. To date, multiple bZIPs have been identified and investigated in numerous plant species. However, few studies have characterized...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Zheng W,Xie T,Yu X,Chen N,Zhang Z

    更新日期:2020-01-01 00:00:00

  • Characterizing miRNA and mse-tsRNA in fertile and subfertile yak bull spermatozoa from Arunachal Pradesh.

    abstract::Male fertility in farm animals is considered as an important economic trait. The phenomenon of spermatogenesis plays a dynamic functional role in determining the viability of sperm and thereby can impact on fertility-driven complications. The process of spermatogenesis is controlled by numerous molecular factors and r...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Pratim Das P,Sultana Begum S,Choudhury M,Medhi D,Paul V,Jyoti Das P

    更新日期:2020-01-01 00:00:00

  • Genetic dissection of yield associated traits in a cross between cowpea and yard-long bean (Vigna unguiculata (L.) Walp.) based on DArT markers.

    abstract::Both cowpea and yard-long bean belong to Vigna unguiculata ssp. unguiculata but have diverged through human induced evolution in sub-Saharan Africa and Asia, respectively. To map the quantitative trait loci (QTLs) for yield associated traits and derive new lines that may combine the attributes of both types, we develo...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Garcia-Oliveira AL,Zana Zate Z,Olasanmi B,Boukar O,Gedil M,Fatokun C

    更新日期:2020-01-01 00:00:00

  • Mitogenome analysis of dwarf pufferfish (Carinotetraodon travancoricus) endemic to southwest India and its implications in the phylogeny of Tetraodontidae.

    abstract::The Tetraodontidae (pufferfishes), is primarily a family of marine and estuarine fishes with a limited number of freshwater species. Freshwater invasions can be observed in South America, Southeast Asia and central Africa. In the present study, we have analysed the complete mitogenome of freshwater pufferfish, Carinot...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Sathyajith C,Yamanoue Y,Yokobori SI,Thampy S,Vattiringal Jayadradhan RK

    更新日期:2019-12-01 00:00:00

  • Narrow gene pool can threaten the survival of Calamus nagbettai R. R. Fernald & Dey: a highly, endemic dioecious rattan species in the Western Ghats of India.

    abstract::Rattans, the spiny climbing palms of Arecaceae (Palmae) family exhibit high endemism to the biodiversity hot spots in India. Of the five rattan genera, Calamus is the only genus found in peninsular India with 15 of 21 species, endemic to the Western Ghats. The extensive utilization of rattans owing to their strength, ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Dev SA,Balakrishnan S,Kurian A,Sreekumar VB

    更新日期:2019-11-01 00:00:00

  • Genes involved in the deformations of the shoot apical meristem in somatic embryos of Capsicum chinense Jacq.

    abstract::Somatic embryos (SE) of habanero pepper (Capsicum chinense Jacq.) represent persistent deformations in the shoot apical meristem (SAM), which inhibits their capacity to form organs and subsequently plants. In dicotyledonous plants, SAM is formed in the apex, between cotyledons and it plays a central role in postembryo...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Regla-Márquez CF,Avilés-Viñas SA,Canto-Flick A,Muñoz-Ramírez LS,Peña-Yam LP,Valle-Gough RE,Osorio-Montalvo PM,Pérez-Pastrana J,Santana-Buzzy N

    更新日期:2019-09-01 00:00:00

  • Genetics of fruit yield and its component traits under different fruiting habit backgrounds in chilli (Capsicum annuum L.).

    abstract::The six basic generations (two parents, F1, F2 and backcrosses) of 14 crosses developed from nine parents differing in fruits node-1 and fruit orientation were evaluated to decipher the genetics of three quantitative traits (average fruit weight, fruits plant-1 and green fruit yield plant-1) during the rainly season o...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Anilkumar C,Mohan Rao A,Ramesh S,Bhavani B,Pranesh

    更新日期:2019-09-01 00:00:00

  • Association between genetic polymorphisms of long noncoding RNA H19 and cancer risk: a meta-analysis.

    abstract::Long noncoding RNA (lncRNA) H19, a well-known oncogenic lncRNA, is overexpressed in various cancers. Several studies have investigated the association between polymorphisms in lncRNA H19 and the risk of various cancer types; however, the findings were inconsistent. In this study, we performed a meta-analysis to identi...

    journal_title:Journal of genetics

    pub_type: 杂志文章,meta分析,评审

    doi:

    authors: Hashemi M,Moazeni-Roodi A,Sarabandi S,Karami S,Ghavami S

    更新日期:2019-09-01 00:00:00

  • Detection of QTL for panicle architecture in F2 population of rice.

    abstract::Panicle traits are the most important agronomic characters which directly relate to yield in rice. Panicle length (PL) being one of the major components of rice panicle structure is controlled by quantitative trait loci (QTLs). In our research, conducted at Research Farm of SKUAST-J, crosses of parental lines K343 and...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Bhat R,Singh AK,Salgotra RK,Sharma M,Mushtaq M,Bagati S,Hangloo S,Singh A

    更新日期:2019-06-01 00:00:00

  • Correlation analysis of mandarin fish (Siniperca chuatsi) growth hormone gene polymorphisms and growth traits.

    abstract::Screening of trait-associated molecular markers can be used to enhance the efficiency of selective breeding. Previously, we produced the first high-density genetic linkage map for the mandarin fish (Siniperca chuatsi) and identified 11 quantitative-trait loci significantly associated with growth, of which one is locat...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Sun CF,Sun HL,Dong JJ,Tian YY,Hu J,Ye X

    更新日期:2019-06-01 00:00:00

  • Association between KIAA0319 SNPs and risk of dyslexia: a meta-analysis.

    abstract::The aetiology of developmental dyslexia (DD) is complex; although candidate genes have been suggested, the molecular mechanism and risk factors remain unknown. The KIAA0319 gene is functionally related to neuronal migration and axon growth, and several studies have examined associations between KIAA0319 polymorphisms ...

    journal_title:Journal of genetics

    pub_type: 杂志文章,meta分析

    doi:

    authors: Deng KG,Zhao H,Zuo PX

    更新日期:2019-06-01 00:00:00

  • Genetic diversity and population structure of two endemic Cupressus (Cupressaceae) species on the Qinghai-Tibetan plateau.

    abstract::Cupressus gigantea and C. torulosa are ecologically and economically important endemic species of the conifer family Cupressaceae on the Qinghai-Tibetan plateau. C. gigantea was previously classified as a subspecies of C. torulosa because of their similar morphological characteristics and close distribution. In this s...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Fu Y,Li S,Guo Q,Zheng W,Yang R,Li H

    更新日期:2019-03-01 00:00:00

  • Matrix metalloproteinase gene polymorphisms in chronic periodontitis: a case-control study in the Indian population.

    abstract::Chronic periodontitis (CP) is the common form of inflammatory oral disease. Matrix metalloproteinases (MMPs) play a pivotal role in the progression of CP by degrading gingival tissue and its remodelling. Here, we conducted a case-control study to investigate a possible association of single-nucleotide polymorphism of ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Majumder P,Ghosh S,Dey SK

    更新日期:2019-03-01 00:00:00

  • Novel mutation of type-1 insulin-like growth factor receptor (IGF-1R) gene in a severe short stature pedigree identified by targeted next-generation sequencing.

    abstract::Insulin-like growth factor receptor (IGF-1R) deficiency is a rare form of short stature, and is difficult to clinically diagnose. Targeted next-generation sequencing (NGS) allows for the rapid and inexpensive assessment of short stature. We identified mutations in the pedigree of a Chinese boy with severe short statur...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Yang Y,Huang H,Chen K,Yang L,Xie LL,Xiong T,Wu X

    更新日期:2019-03-01 00:00:00

  • MiR-27b promotes sheep skeletal muscle satellite cell proliferation by targeting myostatin gene.

    abstract::To investigate the role of miR-27b in sheep skeletal muscle development, here we first cloned the sequence of sheep pre-miR-27b, then further investigated its expression pattern in sheep skeletal muscle in vivo, the relationship of miR-27b expression and sheep skeletal muscle satellite cell proliferation and different...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Zhang W,Wang SY,Deng SY,Gao L,Yang LW,Liu XN,Shi GQ

    更新日期:2018-12-01 00:00:00

  • Genetic analysis of signal peptides in amphibian antimicrobial secretions.

    abstract::Amphibian secretion is an important source of bioactive molecules that naturally protect the skin against noxious microorganisms. Collectively called antimicrobial peptides (AMPs), these molecules have a wide spectrum of action, targeting viruses, bacteria and fungi. Like many membrane and secreted proteins, AMPs have...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Pérez LO,Cancelarich NL,Aguilar S,Basso NG,Marani MM

    更新日期:2018-12-01 00:00:00

  • Analysis of novel domain-specific mutations in the zebrafish ndr2/cyclops gene generated using CRISPR-Cas9 RNPs.

    abstract::Nodal-related protein (ndr2) is amember of the transforming growth factor type β superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene encoding nodal cause holoprosencephaly and heterotaxy. Mutations in the ndr2 gene...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Turner AN,Andersen RS,Bookout IE,Brashear LN,Davis JC,Gahan DM,Davis JC,Gotham JP,Hijaz BA,Kaushik AS,Mcgill JB,Miller VL,Moseley ZP,Nowell CL,Patel RK,Rodgers MC,Patel RK,Shihab YA,Walker AP,Glover SR,Foster SD,

    更新日期:2018-12-01 00:00:00

  • A genetic system on chromosome arm 1BL of wild emmer causes distorted segregation in common wheat.

    abstract::Nonrandom segregation ratios of alleles 'segregation distortion' can have a striking impact on transmission genetics, and with widespread availability of genetic markers has been shown to be a frequent phenomenon. To investigate the possible effect of genetic interaction on segregation distortion and genetic map const...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Miao Y,Yang S,Jiang Y,Rong J,Yu J

    更新日期:2018-12-01 00:00:00

  • Genetics of ulcerative colitis: putting into perspective the incremental gains from Indian studies.

    abstract::Ulcerative colitis (UC), one of the two clinical subtypes of inflammatory bowel disease is perceived as a potential 'sleeping giant' in the Indian subcontinent. Clinical manifestation is overall believed to be the same across ethnic groups but overwhelming genetics from large European and fewer non-European studies ha...

    journal_title:Journal of genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Juyal G,Sood A,Midha V,Thelma BK

    更新日期:2018-12-01 00:00:00

  • Genomewide association study for economic traits in the large yellow croaker with different numbers of extreme phenotypes.

    abstract::A traditional genomewide association study (GWAS) detects genotype-phenotype associations by the vast number of genotyped individuals. This method requires large-scale samples and considerable sequencing costs. Extreme phenotypic sampling proposes make GWAS more cost-efficient and are applied more widely. With extreme...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Wan L,Dong L,Xiao S,Han Z,Wang X,Wang Z

    更新日期:2018-09-01 00:00:00

  • Novel alternatively spliced isoforms of MEF2A and their mRNA expression patterns in pigs.

    abstract::The present study aimed to identify the alternatively spliced isoforms of pig MEF2A gene and to determine theirmRNA expression patterns. Four alternatively spliced isoforms of pig MEF2A gene (i.e. MEF2A1, MEF2A2, MEF2A3 and MEF2A4) were cloned according to the results of transcriptome sequencing. The fifth to eighth e...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Guo XH,Zhang Q,Li M,Gao PF,Cao GQ,Cheng ZM,Zhang NF,Yu Le B,Liu JF,Liu XJ,Li BG

    更新日期:2018-09-01 00:00:00

  • A minimum requirements method to isolate large quantities of highly purified DNA from one drop of poultry blood.

    abstract::Here, we describe a rapid, efficient and noncomplicated method for extracting poultry genomic DNA. This simple method obtains excellent qualities of molecular biology grade DNA in a matter of only about 15 min. A straightforward protocol is followed in this extraction procedure, in which, when the blood cells are plac...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Al-Shuhaib MBS

    更新日期:2018-08-24 00:00:00

  • Advances in the discovery of genetic risk factors for complex forms of neurodegenerative disorders: contemporary approaches, success, challenges and prospects.

    abstract::Neurodegenerative diseases constitute a large proportion of disorders in elderly, majority being sporadic in occurrence with ∼5-10% familial. A strong genetic component underlies the Mendelian forms but nongenetic factors together with genetic vulnerability contributes to the complex sporadic forms. Several gene disco...

    journal_title:Journal of genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Kumar S,Yadav N,Pandey S,Thelma BK

    更新日期:2018-07-01 00:00:00

  • Shared mechanisms among neurodegenerative diseases: from genetic factors to gene networks.

    abstract::Neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis are pressing health concerns in modern societies for which effective therapies are still lacking. Recent high-throughput genomic technologies have enabled genome-scale, multidimensional investigations to faci...

    journal_title:Journal of genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Arneson D,Zhang Y,Yang X,Narayanan M

    更新日期:2018-07-01 00:00:00

  • Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population.

    abstract::Recurrent spontaneous abortions (RSA) is defined as three or more consecutive pregnancy losses before 20 weeks of gestation. Various causes of RSA have been identified, still 50% cases remain unexplained after evaluation. One of the causes of unexplained recurrent spontaneous abortions (URSA) is supposed to be the dis...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Mishra S,Srivastava A,Mandal K,Phadke SR

    更新日期:2018-06-01 00:00:00

  • A genome scan for quantitative trait loci affecting average daily gain and Kleiber ratio in Baluchi Sheep.

    abstract::Genomewide association study (GWAS) is an efficient tool for the detection of SNPs and candidate genes in quantitative traits. Growth rate is an important trait for increasing the meat production in sheep. A total of 96 Baluchi sheep were genotyped using Illumina Ovine SNP50 BeadChip to run a GWAS for an average daily...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Pasandideh M,Rahimi-Mianji G,Gholizadeh M

    更新日期:2018-06-01 00:00:00

  • Y-chromosome polymorphisms of the domestic Bactrian camel in China.

    abstract::Single-nucleotide polymorphisms (SNPs), microsatellites and copy number variation (CNV) were studied on the Y chromosome to understand the paternal origin and phylogenetic relationships for resource protection, rational development and utilization of the domestic Bactrian camel in China. Our sample set consisted of 94...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Chen H,Ren Z,Zhao J,Zhang C,Yang X

    更新日期:2018-03-01 00:00:00

  • Whitefly and aphid inducible promoters of Arabidopsis thaliana L.

    abstract::Lack of regulated expression and tissue specificity are the major drawbacks of plant and virus-derived constitutive promoters. A precise tissue or site-specific expression, facilitate regulated expression of proteins at the targeted time and site. Publically available microarray data on whitefly and aphid infested Ara...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Dubey NK,Mishra DK,Idris A,Nigam D,Singh PK,Sawant SV

    更新日期:2018-03-01 00:00:00

  • Genetic variants of FOXP1 and FOXF1 are associated with the susceptibility of oesophageal adenocarcinoma in Chinese population.

    abstract::This study aimed to investigate whether the genetic variants of CRTC1, BARX1, FOXP1 and FOXF1 are associated with the development of oesophageal adenocarcinoma (OA) in Chinese population. A total of 744 OA patients and 1138 controls were included in this study. Here we genotyped four SNPs, rs10419226 of CRTC1, rs11789...

    journal_title:Journal of genetics

    pub_type: 杂志文章,多中心研究

    doi:

    authors: Zhang J,Chen J,Ma T,Guo H,Yang B

    更新日期:2018-03-01 00:00:00

  • Case report of newborn with de novo partial trisomy 2q31.2-37.3 and monosomy 9p24.3.

    abstract::We describe a newborn female with a de novo duplication of chromosomes 2q31.2 and 2q37.3, and a de novo monosomy 9p24.3. The clinical findings of this patient include congenital heart defects, dysmorphic facial features, hypotonia, feeding difficulties and microcephaly. Ultrasonographic prenatal findings were negative...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Colangelo M,Alfonsi M,Palka C,Zio EZ,Renzo SD,Guanciali-Franchi P,Palka G

    更新日期:2018-03-01 00:00:00

  • Neuro-fuzzy model of homocysteine metabolism.

    abstract::In view of well-documented association of hyperhomocysteinaemia with a wide spectrum of diseases and higher incidence of vitamin deficiencies in Indians, we proposed a mathematical model to forecast the role of demographic and genetic variables in influencing homocysteinemetabolism and investigated the influence of li...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0856-x

    authors: Naushad SM,Rama Devi AR,Nivetha S,Lakshmitha G,Stanley AB,Hussain T,Kutala VK

    更新日期:2017-12-01 00:00:00

  • Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.

    abstract::Ellis-van Creveld syndrome is an autosomal recessive skeletal dysplasia primarily characterized by the features such as disproportionate dwarfism, short ribs, short limbs, dysplastic nails, cardiovascular malformations, post-axial polydactyly (PAP) (bilateral) of hands and feet. EVC/EVC2 located in head-to-head arrang...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0868-6

    authors: Umair M,Seidel H,Ahmed I,Ullah A,Haack TB,Alhaddad B,Jan A,Rafique A,Strom TM,Ahmad F,Meitinger T,Ahmad W

    更新日期:2017-12-01 00:00:00

  • J. B. S. Haldane and the origin of life.

    abstract::In 1929 the British biologist John Burdon Sanderson Haldane published a hypothesis on the origin of life on earth, which was one of the most emblematic of the interwar period. It was a scenario describing the progressive evolution of matter on the primitive earth and the emergence of life. Firstly, this paper presents...

    journal_title:Journal of genetics

    pub_type: 传,历史文章,杂志文章

    doi:10.1007/s12041-017-0831-6

    authors: Tirard S

    更新日期:2017-11-01 00:00:00

  • Fitness differences due to allelic variation at Esterase-4 locus in Drosophila ananassae.

    abstract::Esterases are known to play essential role inmetabolism, reproductive physiology and behaviour of Drosophila. Esterases are highly polymorphic enzymes in Drosophila, but the polymorphism of these enzymes is not well studied in Drosophila ananassae. Recent studies on esterase polymorphism in D. ananassae revealed that ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0814-7

    authors: Krishnamoorti K,Singh AK

    更新日期:2017-09-01 00:00:00

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