Works matching Human abnormalities
Results: 5000
Deep Maxout Network for human action and abnormality detection using Chronological Poor and Rich Optimization.
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- Computer Methods in Biomechanics & Biomedical Engineering: Imaging & Visualisation, 2023, v. 11, n. 3, p. 758, doi. 10.1080/21681163.2022.2111720
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- Article
S-WD-EEMD: A hybrid framework for imbalanced sEMG signal analysis in diagnosis of human knee abnormality.
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- PLoS ONE, 2024, v. 19, n. 5, p. 1, doi. 10.1371/journal.pone.0301263
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- Article
CASA derived human sperm abnormalities: correlation with chromatin packing and DNA fragmentation.
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- Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 12, p. 1327, doi. 10.1007/s10815-012-9885-9
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- Article
Analysing human developmental abnormalities.
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- BioEssays, 1996, v. 18, n. 12, p. 965, doi. 10.1002/bies.950181206
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- Article
Imperfecta: Her brother's disease leads a writer to challenge how we conceive of human abnormality in the emerging era of gene editing.
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- American Scholar, 2024, v. 93, n. 3, p. 27
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- Article
In Silico Analysis of Collagens Missense SNPs and Human Abnormalities.
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- Biochemical Genetics, 2022, v. 60, n. 5, p. 1630, doi. 10.1007/s10528-021-10172-6
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- Article
Rheological Abnormalities in Human Erythrocytes Subjected to Oxidative Inflammation.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.837926
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- Article
Developmental Origins of Limb Developmental Instability in Human Fetuses: Many Abnormalities Make the Difference.
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- Symmetry (20738994), 2017, v. 9, n. 4, p. 51, doi. 10.3390/sym9040051
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- Article
Supplementary Pharmacotherapy for the Behavioral Abnormalities Caused by Stressors in Humans, Focused on Post-Traumatic Stress Disorder (PTSD).
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- Journal of Clinical Medicine, 2023, v. 12, n. 4, p. 1680, doi. 10.3390/jcm12041680
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- Article
Structural abnormalities in the human diaphragm in drowning and hanging deaths: preliminary results.
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- Forensic Science, Medicine & Pathology, 2020, v. 16, n. 2, p. 265, doi. 10.1007/s12024-020-00235-2
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- Article
Chromosome Abnormalities in the Human Oocyte.
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- Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 107, doi. 10.1159/000323801
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- Article
C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome.
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- Cytogenetic & Genome Research, 2006, v. 112, n. 1/2, p. 16, doi. 10.1159/000087509
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- Article
Frequency and distribution of chromosome abnormalities in human oocytes.
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- Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 193, doi. 10.1159/000086889
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- Publication type:
- Article
Frequency and distribution of chromosome abnormalities in human spermatozoa.
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- Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 199, doi. 10.1159/000086890
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- Article
The Impact of Acquired Genetic Abnormalities on the Clinical Translation of Human Pluripotent Stem Cells.
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- Cells (2073-4409), 2021, v. 10, n. 11, p. 3246, doi. 10.3390/cells10113246
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- Article
Chromosome Structural Alteration an Unusual Abnormality Characterizing Human Neoplasia.
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- Novelty in Biomedicine, 2016, n. 2, p. 77
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- Article
INSIGHT INTO HUMAN CONGENITAL ABNORMALITY.
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- Reproductive Sciences, 2007, v. 14, n. 4, p. 295, doi. 10.1177/1933719107304304
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- Article
Detection of Abnormalities in COVID-19 Infected Human Respiratory System using Accelerometer with the aid of Machine Learning.
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- International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 4, p. 3399, doi. 10.31838/ijpr/2020.12.04.464
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- Article
Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.
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- Clinical Genetics, 2019, v. 96, n. 5, p. 385, doi. 10.1111/cge.13602
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- Article
Advanced age increases chromosome structural abnormalities in human spermatozoa.
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- European Journal of Human Genetics, 2011, v. 19, n. 2, p. 145, doi. 10.1038/ejhg.2010.166
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- Publication type:
- Article
Behavioral and neural network abnormalities in human APP transgenic mice resemble those of App knock-in mice and are modulated by familial Alzheimer's disease mutations but not by inhibition of BACE1.
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- Molecular Neurodegeneration, 2020, v. 15, n. 1, p. N.PAG, doi. 10.1186/s13024-020-00393-5
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- Article
Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.
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- Neuropathology, 2014, v. 34, n. 3, p. 219, doi. 10.1111/neup.12081
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- Article
Natural Polyphenols May Normalize Hypochlorous Acid-Evoked Hemostatic Abnormalities in Human Blood.
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- Antioxidants, 2022, v. 11, n. 4, p. N.PAG, doi. 10.3390/antiox11040779
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- Article
Novel variants in TUBB8 gene cause multiple phenotypic abnormalities in human oocytes and early embryos.
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- Journal of Ovarian Research, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13048-023-01274-3
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- Article
The prevalence of liver abnormalities in humans due to Schistosoma japonicum by ultrasonography in China: a meta-analysis.
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- 2022
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- Publication type:
- journal article
Comparison of unstimulated and stimulated behaviour in human fetuses with congenital abnormalities.
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- 1999
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- Publication type:
- journal article
A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S24, doi. 10.1016/S1472-6483(10)62320-6
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- Publication type:
- Article
Hyperglycemia-Induced Abnormalities in Rat and Human Corneas: The Potential of Second Harmonic Generation Microscopy.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048388
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- Publication type:
- Article
Chia (Salvia hispanica)-supplemented diet ameliorates non-alcoholic fatty liver disease and its metabolic abnormalities in humans.
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- Lipids in Health & Disease, 2020, v. 19, n. 1, p. 1, doi. 10.1186/s12944-020-01283-x
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- Article
Meiotic errors in human oogenesis and spermatogenesis.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, n. 4, p. 523, doi. 10.1016/S1472-6483(10)60459-2
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- Publication type:
- Article
Trichorhinophalangeal syndrome type II associated with aplasia cutis congenita in a neonate.
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- Pediatric Dermatology, 2022, v. 39, n. 3, p. 481, doi. 10.1111/pde.14934
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- Article
Human Papillomavirus Infections in Women With and Without Squamous Cell Abnormalities of the Uterine Cervix.
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- Scripta Medica, 2019, v. 50, n. 3, p. 69, doi. 10.5937/scriptamed50-21910
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- Article
ABNORMAL APPEARANCES : INSPECTION, DISPLAY AND THE CLINIC.
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- Medicina nei Secoli: Arte e Scienza, 2014, v. 26, n. 1, p. 333
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- Article
Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes.
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- Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 206, doi. 10.1159/000086891
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- Article
The Electrogenic Na<sup>+</sup>/K<sup>+</sup> Pump Is a Key Determinant of Repolarization Abnormality Susceptibility in Human Ventricular Cardiomyocytes: A Population-Based Simulation Study.
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- Frontiers in Physiology, 2017, v. 8, p. 1, doi. 10.3389/fphys.2017.00278
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- Article
Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals.
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- PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005462
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- Article
Piezo2 expressed in proprioceptive neurons is essential for skeletal integrity.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16971-6
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- Article
Application of low‐wavenumber Raman spectroscopy to the analysis of human teeth.
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- Journal of Raman Spectroscopy, 2019, v. 50, n. 10, p. 1375, doi. 10.1002/jrs.5648
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- Article
A Survey of the Diagnosis of Peripheral Neuropathy Using Intelligent and Wearable Systems.
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- Technologies (2227-7080), 2023, v. 11, n. 6, p. 163, doi. 10.3390/technologies11060163
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- Article
Sperm Abnormality Detection Using Sequential Deep Neural Network.
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- Mathematics (2227-7390), 2023, v. 11, n. 3, p. 515, doi. 10.3390/math11030515
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- Article
Identification of the Mitf gene mutation causing congenital deafness and pigmentation disorders in porcupines using BSA-Seq.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-82975-7
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- Article
Unobtrusive measurement of gait parameters using seismographs: An observational study.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-64508-4
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- Publication type:
- Article
Gaussian Aquila optimizer based dual convolutional neural networks for identification and grading of osteoarthritis using knee joint images.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-57002-4
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- Publication type:
- Article
EP04.13: Parental origin of autosomal trisomies and triploidies prenatally diagnosed by QF‐PCR.
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- Ultrasound in Obstetrics & Gynecology, 2019, v. 54, p. 252, doi. 10.1002/uog.21168
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- Article
OC24.03: Impaired cerebral cortex development in human fetuses with posterior brain abnormalities and diagnosed open neural tube defects at 11-13 weeks.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 56, doi. 10.1002/uog.13621
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- Publication type:
- Article
De novo and inherited micro-CNV at 16p13.11 in 21 Chinese patients with defective cardiac left-right patterning.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1458953
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- Publication type:
- Article
HIGH GLUCOSE EXPOSURE INDUCES ABNORMALITIES IN HUMAN ENDOTHELIAL CELL GROWTH AND DEATH.
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- 2002
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- Abstract
Best laboratory practices and therapeutic interventions to reduce sperm DNA damage.
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- Andrologia, 2021, v. 53, n. 2, p. 1, doi. 10.1111/and.13736
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- Article
Influence of variation in global sperm DNA methylation level on the expression level of protamine genes and human semen parameters.
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- Andrologia, 2020, v. 52, n. 1, p. N.PAG, doi. 10.1111/and.13484
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- Publication type:
- Article
Identification of Copy Number Variation Among Nonsyndromic Cleft Lip and or Without Cleft Palate With Hypodontia: A Genome-Wide Association Study.
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- Frontiers in Physiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphys.2021.637306
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- Publication type:
- Article