Works matching DE "X chromosome"
Results: 3842
Satellitome analysis on Microtus thomasi (Arvicolinae) genome, a mammal species with high karyotype and sex chromosome variations.
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- Genome, 2025, v. 68, p. 1, doi. 10.1139/gen-2024-0141
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- Publication type:
- Article
X-chromosome-linked miR-542-5p as a key regulator of sex disparity in rats with adjuvant-induced arthritis by promoting Th17 differentiation.
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- Biomarker Research, 2025, v. 13, n. 1, p. 1, doi. 10.1186/s40364-025-00741-x
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- Article
Hearing Loss and Turner Syndrome: A Scoping Review.
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- Journal of International Advanced Otology, 2025, v. 21, n. 1, p. 1, doi. 10.5152/iao.2025.241723
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- Article
Severe aplastic anemia with acquired X chromosome clonality as a sole abnormality.
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- Annals of Hematology, 2025, v. 104, n. 1, p. 815, doi. 10.1007/s00277-024-06166-0
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- Article
Investigation of a hemophilia family with one female hemophilia A patient and 12 male hemophilia A patients.
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- Annals of Hematology, 2025, v. 104, n. 1, p. 163, doi. 10.1007/s00277-024-06158-0
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- Article
Androgen receptor dynamics in prostate cancer: from disease progression to treatment resistance.
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- Frontiers in Oncology, 2025, p. 1, doi. 10.3389/fonc.2025.1542811
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- Article
Circadian Rhythms and the Transcriptional Feedback Loop (Nobel Lecture)**.
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 8732, doi. 10.1002/ange.202015199
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- Article
Condition dependence and the nature of genetic variation for male sex comb bristle number in Drosophila melanogaster.
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- Genetica, 2011, v. 139, n. 4, p. 505, doi. 10.1007/s10709-011-9572-2
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- Article
Karyotype analysis of the Russian wheat aphid, Diuraphis noxia (Kurdjumov) (Hemiptera: Aphididae) reveals a large X chromosome with rRNA and histone gene families.
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- Genetica, 2011, v. 139, n. 3, p. 281, doi. 10.1007/s10709-011-9546-4
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- Article
Evidence based on studies of the mus309 mutant, deficient in DNA double-strand break repair, that meiotic crossing over in Drosophila melanogaster is a two-phase process.
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- Genetica, 2010, v. 138, n. 9/10, p. 1033, doi. 10.1007/s10709-010-9489-1
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- Article
High genetic differentiation between an African and a non-African strain of Drosophila simulans revealed by segregation distortion and reduced crossover frequency.
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- Genetica, 2009, v. 137, n. 2, p. 165, doi. 10.1007/s10709-009-9381-z
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- Article
Sequence signatures of a recent chromosomal rearrangement in Drosophila mojavensis.
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- Genetica, 2009, v. 136, n. 1, p. 5, doi. 10.1007/s10709-008-9296-0
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- Publication type:
- Article
Recent duplication and positive selection of the GAGE gene family.
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- Genetica, 2008, v. 133, n. 1, p. 31, doi. 10.1007/s10709-007-9179-9
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- Publication type:
- Article
Identification of putative genetic regions for watermelon rind hardness and related traits by BSA-seq and QTL mapping.
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- Euphytica, 2021, v. 217, n. 2, p. 1, doi. 10.1007/s10681-020-02758-9
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- Article
Loss of function of male‐specific lethal 3 (Msl3) does not affect spermatogenesis in rodents.
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- Developmental Dynamics, 2024, v. 253, n. 5, p. 453, doi. 10.1002/dvdy.669
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- Article
Coexistence of a Choriocarcinoma and a Gonadoblastoma in the Gonad of a 46,XY Female: A Single Nucleotide Polymorphism Array Analysis.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 1, p. 66, doi. 10.2350/09-02-0606-CR.1
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- Article
Regulatory mechanism and biological function of UHRF1–DNMT1-mediated DNA methylation.
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- Functional & Integrative Genomics, 2022, v. 22, n. 6, p. 1113, doi. 10.1007/s10142-022-00918-9
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- Publication type:
- Article
Transcriptome-wide identification and characterization of microRNAs responsive to phosphate starvation in Populus tomentosa.
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- Functional & Integrative Genomics, 2019, v. 19, n. 6, p. 953, doi. 10.1007/s10142-019-00692-1
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- Article
Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome.
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- Functional & Integrative Genomics, 2013, v. 13, n. 3, p. 285, doi. 10.1007/s10142-013-0323-6
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- Article
Small RNA sequencing analysis reveals regulation of microRNA expression in Madin–Darby canine kidney epithelial cells infected with Canid alphaherpesvirus 1.
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- Virus Genes, 2024, v. 60, n. 5, p. 537, doi. 10.1007/s11262-024-02091-6
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- Publication type:
- Article
A Case of 46,X,der(X)t(X;X)(q22.1;p11) Xq22.1→Xqter in a 12-Year-Old Girl with Premature Ovarian Failure.
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- Gynecologic & Obstetric Investigation, 2007, v. 63, n. 3, p. 137, doi. 10.1159/000096436
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- Article
Involvement of the Streptococcus mutans PgfE and GalE 4-epimerases in protein glycosylation, carbon metabolism, and cell division.
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- Glycobiology, 2023, v. 33, n. 3, p. 245, doi. 10.1093/glycob/cwad004
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- Article
Dynamic Patterns of Sex Chromosome Evolution in Neognath Birds: Many Independent Barriers to Recombination at the ATP5F1A Locus.
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- Birds (2673-6004), 2022, v. 3, n. 1, p. 51, doi. 10.3390/birds3010004
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- Article
Fragile-X-associated Tremor/Ataxia Syndrome (FXTAS) in a Female with FMR1 Premutation: Case Report.
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- 2022
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- Publication type:
- Case Study
A roadmap for comparative primate coloration research: a response to comments on Caro et al.
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- Behavioral Ecology, 2021, v. 32, n. 4, p. 572, doi. 10.1093/beheco/arab075
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- Article
What is primate color vision for? a comment on Caro et al.
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- Behavioral Ecology, 2021, v. 32, n. 4, p. 571, doi. 10.1093/beheco/arab050
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- Article
Effect of color vision phenotype on the foraging of wild white-faced capuchins, Cebus capucinus.
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- Behavioral Ecology, 2007, v. 18, n. 2, p. 292, doi. 10.1093/beheco/arl082
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- Article
Clinical spectrum and Cytogenetic characterization of patients with Turner Syndrome – Twin case report.
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- 2022
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- Publication type:
- Case Study
The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development.
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- Communications Biology, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s42003-025-07699-4
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- Article
Circulating DNA reveals a specific and higher fragmentation of the Y chromosome.
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- Human Genetics, 2023, v. 142, n. 11, p. 1603, doi. 10.1007/s00439-023-02600-x
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- Article
CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome.
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- Human Genetics, 2023, v. 142, n. 4, p. 523, doi. 10.1007/s00439-023-02538-0
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- Article
Hemizygosity can reveal variant pathogenicity on the X-chromosome.
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- Human Genetics, 2023, v. 142, n. 1, p. 11, doi. 10.1007/s00439-022-02478-1
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- Article
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation.
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- Human Genetics, 2022, v. 141, n. 7, p. 1279, doi. 10.1007/s00439-021-02400-1
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- Article
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier.
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- Human Genetics, 2021, v. 140, n. 5, p. 775, doi. 10.1007/s00439-020-02242-3
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- Article
Editorial for the special issue on the molecular genetics of male infertility.
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- 2021
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- Publication type:
- Editorial
The X chromosome and male infertility.
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- Human Genetics, 2021, v. 140, n. 1, p. 203, doi. 10.1007/s00439-019-02101-w
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- Publication type:
- Article
Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD).
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- Human Genetics, 2019, v. 138, n. 11/12, p. 1409, doi. 10.1007/s00439-019-02077-7
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- Publication type:
- Article
Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair.
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- Human Genetics, 2019, v. 138, n. 11/12, p. 1313, doi. 10.1007/s00439-019-02075-9
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- Publication type:
- Article
Expanding the phenotype of the X-linked BCOR microphthalmia syndromes.
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- Human Genetics, 2019, v. 138, n. 8/9, p. 1051, doi. 10.1007/s00439-018-1896-x
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- Article
Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.
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- Human Genetics, 2017, v. 136, n. 11/12, p. 1395, doi. 10.1007/s00439-017-1838-z
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- Publication type:
- Article
Slower-X: reduced efficiency of selection in the early stages of X chromosome evolution.
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- Evolution Letters, 2023, v. 7, n. 1, p. 4, doi. 10.1093/evlett/qrac004
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- Article
Divergence and introgression among the virilis group of Drosophila.
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- Evolution Letters, 2022, v. 6, n. 6, p. 537, doi. 10.1002/evl3.301
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- Publication type:
- Article
How much does the unguarded X contribute to sex differences in life span?
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- Evolution Letters, 2022, v. 6, n. 4, p. 319, doi. 10.1002/evl3.292
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- Article
Experimental evolution reveals sex‐specific dominance for surviving bacterial infection in laboratory populations of Drosophila melanogaster.
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- Evolution Letters, 2021, v. 5, n. 6, p. 657, doi. 10.1002/evl3.259
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- Article
Experimental evolution supports signatures of sexual selection in genomic divergence.
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- Evolution Letters, 2021, v. 5, n. 3, p. 214, doi. 10.1002/evl3.220
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- Article
Field cricket genome reveals the footprint of recent, abrupt adaptation in the wild.
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- Evolution Letters, 2020, v. 4, n. 1, p. 19, doi. 10.1002/evl3.148
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- Article
Tightly linked antagonistic‐effect loci underlie polygenic phenotypic variation in C. elegans.
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- Evolution Letters, 2019, v. 3, n. 5, p. 462, doi. 10.1002/evl3.139
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- Publication type:
- Article
Worse than nothing at all: the inequality of fusions joining autosomes to the PAR and non-PAR portions of sex chromosomes.
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- PeerJ, 2024, p. 1, doi. 10.7717/peerj.17740
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- Article
Exploring the roles of ZmARM gene family in maize development and abiotic stress response.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.16254
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- Article
Sex differences in gene expression and alternative splicing in the Chinese horseshoe bat.
- Published in:
- PeerJ, 2023, p. 1, doi. 10.7717/peerj.15231
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- Publication type:
- Article