Works about HUMAN chromosomes
Results: 2308
Cortex-Specific Tmem169 Deficiency Induces Defects in Cortical Neuron Development and Autism-Like Behaviors in Mice.
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- Journal of Neuroscience, 2025, v. 45, n. 9, p. 1, doi. 10.1523/JNEUROSCI.1072-24.2024
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- Article
DOES CYPRUS NEED A TRUTH AND RECONCILIATION COMMISSION?
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- Cyprus Review, 2007, v. 19, n. 1, p. 71
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- Article
Regions of Unusually High Flexibility Occur Frequently in Human Genomic DNA.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 3, p. 612, doi. 10.1271/bbb.120850
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- Article
Perilobar Nephrogenic Rests and Chromosome 22.
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- Pediatric & Developmental Pathology, 2011, v. 14, n. 6, p. 485, doi. 10.2350/10-01-0781-CR.1
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- Article
Differential Detection of Deletion 22q11.2 Syndrome by Specialty and Indication.
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- Pediatric & Developmental Pathology, 2005, v. 8, n. 5, p. 557, doi. 10.1007/s10024-005-0056-1
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- Article
Overexpression of YAP1 induces immortalization of normal human keratinocytes by blocking clonal evolution.
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- Histochemistry & Cell Biology, 2010, v. 134, n. 3, p. 265, doi. 10.1007/s00418-010-0728-4
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- Article
Histone lysine methylation patterns in human cell types are arranged in distinct three-dimensional nuclear zones.
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- Histochemistry & Cell Biology, 2006, v. 125, n. 1/2, p. 3, doi. 10.1007/s00418-005-0049-1
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- Article
Illuminating the human genome.
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- Histochemistry & Cell Biology, 2001, v. 115, n. 1, p. 23, doi. 10.1007/s004180000236
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- Article
Looking through genomics-from the editors.
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- Functional & Integrative Genomics, 2005, v. 5, n. 1, p. 1, doi. 10.1007/s10142-004-0129-7
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- Article
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
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- Archives of Dermatological Research, 2006, v. 298, n. 3, p. 135, doi. 10.1007/s00403-006-0671-3
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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
HP1-Driven Micro-Phase Separation of Heterochromatin-Like Domains/Complexes.
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- Epigenetics Insights, 2022, p. 1, doi. 10.1177/25168657221109766
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- Article
HP1-Driven Micro-Phase Separation of Heterochromatin-Like Domains/Complexes.
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- Epigenetics Insights, 2022, v. 15, p. 1, doi. 10.1177/25168657221109766
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- Article
Inter-3' ends CpG islands are enriched in human chromosome 19p13.3 region: A genomic signature of metabolism-associated genes.
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- Environmental Disease, 2021, v. 6, n. 1, p. 24, doi. 10.4103/ed.ed_4_21
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- Article
A Southeast Asian origin for present-day non-African human Y chromosomes.
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- Human Genetics, 2021, v. 140, n. 2, p. 299, doi. 10.1007/s00439-020-02204-9
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- Article
Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome.
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- Human Genetics, 2020, v. 139, n. 12, p. 1555, doi. 10.1007/s00439-020-02196-6
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- Article
Mosaic loss of human Y chromosome: what, how and why.
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- Human Genetics, 2020, v. 139, n. 4, p. 421, doi. 10.1007/s00439-020-02114-w
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- Article
Characterization of Orphan Human Cytochromes P450.
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- Drug Metabolism Reviews, 2007, v. 39, n. 2/3, p. 627, doi. 10.1080/03602530701467708
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- Article
Polymorphic Cytochrome P450 2D6: Humanized Mouse Model and Endogenous Substrates.
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- Drug Metabolism Reviews, 2004, v. 36, n. 2, p. 243, doi. 10.1081/DMR-120034000
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- Article
403. DISCOVERY P450 INHIBITION SCREENING: HOW DOES A 5-IN-1 LC-MS/MS ASSAY COMPARE TO COMMONLY USED FLUOROMETRIC ASSAYS?
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- 2002
- Publication type:
- Abstract
Comprehensive analyses of genetic diversities and population structure of the Guizhou Dong group based on 44 Y-markers.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.16183
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- Article
Integrated bioinformatics analysis for the identification of hub genes and signaling pathways related to circANRIL.
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- PeerJ, 2022, p. 1, doi. 10.7717/peerj.13135
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- Article
Leroy Hood Looks Forward to P4 Medicine: Predictive, Personalized, Preventive, and Participatory.
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- JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 12, p. 1, doi. 10.1093/jnci/dju416
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- Article
Association Between Two Unlinked Loci at 8q24 and Prostate Cancer Risk Among European Americans.
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- JNCI: Journal of the National Cancer Institute, 2007, v. 99, n. 20, p. 1525, doi. 10.1093/jnci/djm169
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- Article
Mapping QTL for osteoarthritis in dogs.
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- Journal of Animal Science, 2006, v. 84, p. 162
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- Article
Structural insights into human CCAN complex assembled onto DNA.
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- Cell Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41421-022-00439-6
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- Article
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset.
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- Neurological Sciences, 2021, v. 42, n. 11, p. 4759, doi. 10.1007/s10072-021-05480-z
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- Article
General Designs Reveal a Purine-Pyrimidine Structural Code in Human DNA.
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- Mathematics (2227-7390), 2022, v. 10, n. 15, p. 2723, doi. 10.3390/math10152723
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- Article
Comparative mapping of anchor loci from HSA19 to cattle chromosomes 7 and 18.
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- Journal of Heredity, 1997, v. 88, n. 6, p. 524, doi. 10.1093/oxfordjournals.jhered.a023149
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- Article
Inheritance of Dermatoglyphic Asymmetry and Diversity Traits in Twins Based on Factor: Variance Decomposition Analysis.
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- Collegium Antropologicum, 2013, v. 37, n. 2, p. 537
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- Article
Expression Profiling of Genes Involved in the Development and Function of Skeletal Muscles in Ts1Cje Mouse Model of Down Syndrome.
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- Malaysian Journal of Medicine & Health Sciences, 2018, v. 14, n. SP1, p. 12
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- Article
Prediction of Centromere Location in Human Chromosome Using Convolutional Neural Networks.
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- TEM Journal, 2023, v. 12, n. 3, p. 1242, doi. 10.18421/TEM123-02
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- Article
Extrarenal rhabdoid tumors of soft tissue: Clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features.
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- Pathology International, 2006, v. 56, n. 6, p. 287, doi. 10.1111/j.1440-1827.2006.01962.x
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- Article
Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12.
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- Experimental Dermatology, 2001, v. 10, n. 2, p. 90, doi. 10.1034/j.1600-0625.2001.010002090.x
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- Article
Polymorphic Rearrangements of Human Chromosome 9 and Male Infertility: New Evidence and Impact on Spermatogenesis.
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- Biomolecules (2218-273X), 2023, v. 13, n. 5, p. 729, doi. 10.3390/biom13050729
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- Article
Matrix Metalloproteinases Contribute to the Calcification Phenotype in Pseudoxanthoma Elasticum.
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- Biomolecules (2218-273X), 2023, v. 13, n. 4, p. 672, doi. 10.3390/biom13040672
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- Article
The Regulatory Mechanism of miR-574-5p Expression in Cancer.
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- Biomolecules (2218-273X), 2023, v. 13, n. 1, p. 40, doi. 10.3390/biom13010040
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- Article
Role of 3-Mercaptopyruvate Sulfurtransferase in the Regulation of Proliferation and Cellular Bioenergetics in Human Down Syndrome Fibroblasts.
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- Biomolecules (2218-273X), 2020, v. 10, n. 4, p. 653, doi. 10.3390/biom10040653
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- Article
Paraoxonase 3: Structure and Its Role in Pathophysiology of Coronary Artery Disease.
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- Biomolecules (2218-273X), 2019, v. 9, n. 12, p. 817, doi. 10.3390/biom9120817
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- Article
Impaired CENP-E Function Renders Large Chromosomes More Vulnerable to Congression Failure.
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- Biomolecules (2218-273X), 2019, v. 9, n. 2, p. 44, doi. 10.3390/biom9020044
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- Article
Re: Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis. S. C. Hillman, D. J. McMullan, G. Hall, F. S. Togneri, N. James, E. J. Maher, C. H. Meller, D. Williams, R. J. Wapner, E. R. Maher and M. D. Kilby. Ultrasound Obstet Gynecol 2013; 41: 610-620
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- Ultrasound in Obstetrics & Gynecology, 2013, v. 41, n. 6, p. 608, doi. 10.1002/uog.12500
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- Article
Congenital combined deficiency of coagulation factors VII and X - different genetic mechanisms.
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- Haemophilia, 2015, v. 21, n. 3, p. 386, doi. 10.1111/hae.12604
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- Article
Sth1, the Key Subunit of the RSC Chromatin Remodeling Complex, Is Essential in Maintaining Chromosomal Integrity and Mediating High Fidelity Chromosome Segregation in the Human Fungal Pathogen Candida albicans.
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- Frontiers in Microbiology, 2019, p. N.PAG, doi. 10.3389/fmicb.2019.01303
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- Article
Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 7.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1498978
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- Article
Higher-Order Chromatin Structures of Chromosomally Integrated HHV-6A Predict Integration Sites.
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- Frontiers in Cellular & Infection Microbiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fcimb.2021.612656
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- Article
Evidence for Tethering of Human Cytomegalovirus Genomes to Host Chromosomes.
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- Frontiers in Cellular & Infection Microbiology, 2020, v. 10, p. N.PAG, doi. 10.3389/fcimb.2020.577428
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- Article
External validation of karyotype nomogram to predict karyotype abnormalities in oligospermic men.
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- Andrologia, 2022, v. 54, n. 7, p. 1, doi. 10.1111/and.14446
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- Article
Presence of HHV-6 genome in spermatozoa in a context of couples with low fertility: what type of infection?
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- Andrologia, 2015, v. 47, n. 5, p. 531, doi. 10.1111/and.12299
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- Article
Complex Variant of Philadelphia Translocation Involving Chromosomes 9, 12, and 22 in a Case with Chronic Myeloid Leukaemia.
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- 2014
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- Publication type:
- Case Study
Monosomy 21 Seen in Live Born Is Unlikely to Represent True Monosomy 21: A Case Report and Review of the Literature.
- Published in:
- 2014
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- Publication type:
- Case Study