Y deletion
Sexual Dimorphism in White Campion: Deletion on the Y Chromosome Results in a Floral Asexual Phenotype
... is supported by indirect evidence, such as higher rates of bsx mutations as compared with asx mutations ob- tained at low g-ray dosages (Lardon et al. 1999, this issue), together with higher incidences of single vs. dou- ...
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1p36 deletion syndrome: an update
... Since deletion of two or more 1p36-related genes or genomic regions could result in similar phenotypes, it would be unwise to automatically assume that the gene responsible for a specific phenotype must reside ...
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R1 and R2 Retrotransposition and Deletion in the rDNA Loci on the X and Y Chromosomes of Drosophila melanogaster
... the Y in one line were consistently associated with that chromosome across all ...the Y locus in the absence of the X locus, our approach scored all movement of elements from the Y chromosome to the ...
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A New Deletion of the Mouse Y Chromosome Long Arm Associated With the Loss of Ssty Expression, Abnormal Sperm Development and Sterility
... mouse Y chromosome carries 10 distinct genes or gene families that have open reading frames suggestive of retained functionality; it has been assumed that many of these function in ...two Y genes, the ...
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Heterogeneity of DNA deletion in gamma delta beta thalassemia
... The deletion removes the linked epsilon, gamma-, and delta-globin structural genes and terminates within the coding portion of the beta-globin ...DNA deletion in this family differs from that reported in ...
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Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
... promoter deletion variant-transfected cells (less than ...promoter deletion were shown to secrete viral particles by immunoprecipitation and Southern blotting analysis of the culture supernatants ...
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The relationship between hormones level and body mass index with insertion and deletion (D/I) polymorphism of ACE gene in infertile patients with polycystic ovary syndrome
... (ID), Deletion-Deletion (DD)) at three groups: PCOS, infertile patients and control as well as their relationship with hormones level and Body Mass Index (BMI) were ...
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Sentence Compression by Deletion with LSTMs
... The problem formulation we adopt in this paper is very simple: for every token in the input sen- tence we ask whether it should be kept or dropped, which translates into a sequence labeling problem with just two labels: ...
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Identification of the Sex-Determining Region of the Ceratitis capitata Y Chromosome by Deletion Mapping
... The translocation strains have been analyzed geneti- cally and cytogenetically using C-banding of mitotic chromosomes and polytene chromosome analysis to map the au[r] ...
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Apparent uncoupling of oncogenicity from fibroblast transformation and apoptosis in a mutant myc gene transduced by feline leukemia virus.
... The T17 v-myc oncogene was transduced by feline leukemia virus in a spontaneous feline T-cell lymphosar- coma. Molecular cloning and sequencing of the v-myc gene revealed several unique mutations, including a large ...
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Mutational Analysis of the Hypervariable Region of Hepatitis E Virus Reveals Its Involvement in the Efficiency of Viral RNA Replication
... HVR deletion mutants were markedly reduced in Huh7 cells, suggesting a role of the HVR in viral replication ...HVR deletion mutants by using a genetically divergent, nonmam- malian avian HEV, and similar ...
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Functional Interaction of CCR4-NOT Proteins With TATAA-Binding Protein (TBP) and Its Associated Factors in Yeast
... spt3 deletion suppressed the caffeine sensitivity and cold sen- transcription from certain specific nonconsensus TATA sitivity of a ccr4 deletion or a caf1 deletion but did not elements, the not4 and ...
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Statistical Analysis of Fuzzy Linear Regression Model Based on Centroid Method
... By transforming fuzzy data into clear data, the fuzzy linear regression model is transformed into traditional li- near regression model. We study the parameter estimation and impact analysis of the case-deletion ...
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Deletion 22q13.3 syndrome
... karyotyping. Deletion 22q13 has been shown to be one of the common chromosome defects associated with autism ...22q13 deletion syndrome was cited as an example of a genetic disorder characterized by ...
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RadB acts in homologous recombination in the archaeon Haloferax volcanii, consistent with a role as recombination mediator
... also play a role in stabilising nucleoprotein filaments. Deletion of mediator genes leads to defects in recombination and DNA repair. Examples of bacterial recombination mediators include Rec(F)OR, a complex that ...
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Phonological Impairments In The Speech Of Cerebral Palsy Learners Of English As A Second Language
... In the first syllable, the output violates the constraint IDENT PLACE in terms of place of articulation since /r/ is labiodental while /w/ is a bilabial. The output also violated the consonant MAX in the second syllable ...
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Central role of manganese in regulation of stress responses, physiology, and metabolism in streptococcus pneumoniae
... a deletion mutant lacking the solute binding protein of the high-affinity Mn 2 ⴙ transporter, pneumococcal surface antigen A (PsaA), with its isogenic wild-type ...
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A selective EP4 PGE2 receptor agonist alleviates disease in a new mouse model of X linked nephrogenic diabetes insipidus
... X-linked nephrogenic diabetes insipidus (XNDI) is a severe kidney disease caused by inactivating mutations in the V2 vasopressin receptor (V2R) gene that result in the loss of renal urine-concentrating ability. At pres- ...
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Activity of Bdellovibrio Hit Locus Proteins, Bd0108 and Bd0109, Links Type IVa Pilus Extrusion/Retraction Status to Prey-Independent Growth Signalling
... Interestingly, deletion of the adjacent gene, bd0109, was not possible under HI or HD growth conditions; this is discussed later in the results section 2 ∆bd0108 isolates were obtained (∆bd0108#1 and ∆bd0108#2) ...
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Characterization of the 5′-flanking region of the mouse asparagine-linked glycosylation 12 homolog gene
... We characterized each of the Ets family consensus sequences by preparing mutated ALG12 promoter reporter constructs. As shown in Fig. 5C, individual mutations of each Ets-family consensus sequence in the ALG12 promoter ...
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