Works matching Human abnormalities

Results: 5000

Deep Maxout Network for human action and abnormality detection using Chronological Poor and Rich Optimization.

Published in:

Computer Methods in Biomechanics & Biomedical Engineering: Imaging & Visualisation, 2023, v. 11, n. 3, p. 758, doi. 10.1080/21681163.2022.2111720

By:

K L, Bhagya Jyothi;
V, Vasudeva

Publication type:

Article

S-WD-EEMD: A hybrid framework for imbalanced sEMG signal analysis in diagnosis of human knee abnormality.

Published in:

PLoS ONE, 2024, v. 19, n. 5, p. 1, doi. 10.1371/journal.pone.0301263

By:

Vijayvargiya, Ankit;
Sinha, Aparna;
Gehlot, Naveen;
Jena, Ashutosh;
Kumar, Rajesh;
Moran, Kieran

Publication type:

Article

Analysing human developmental abnormalities.

Published in:

BioEssays, 1996, v. 18, n. 12, p. 965, doi. 10.1002/bies.950181206

By:

Winter, Robin M.,

Publication type:

Article

CASA derived human sperm abnormalities: correlation with chromatin packing and DNA fragmentation.

Published in:

Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 12, p. 1327, doi. 10.1007/s10815-012-9885-9

By:

Sivanarayana, T.;
Krishna, Ch.;
Prakash, G.;
Krishna, K.;
Madan, K.;
Rani, B.;
Sudhakar, G.;
Raju, G.

Publication type:

Article

In Silico Analysis of Collagens Missense SNPs and Human Abnormalities.

Published in:

Biochemical Genetics, 2022, v. 60, n. 5, p. 1630, doi. 10.1007/s10528-021-10172-6

By:

Kalmari, Amin;
Heydari, Mohammadkazem;
Hosseinzadeh Colagar, Abasalt;
Arash, Valiollah

Publication type:

Article

Imperfecta: Her brother's disease leads a writer to challenge how we conceive of human abnormality in the emerging era of gene editing.

Published in:

American Scholar, 2024, v. 93, n. 3, p. 27

By:

HAAG, PAMELA

Publication type:

Article

Developmental Origins of Limb Developmental Instability in Human Fetuses: Many Abnormalities Make the Difference.

Published in:

Symmetry (20738994), 2017, v. 9, n. 4, p. 51, doi. 10.3390/sym9040051

By:

ten Broek, Clara M. A.;
Bots, Jessica;
Bugiani, Marianna;
Galis, Frietson;
van Dongen, Stefan

Publication type:

Article

Rheological Abnormalities in Human Erythrocytes Subjected to Oxidative Inflammation.

Published in:

Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.837926

By:

Maruyama, Toru;
Hieda, Michinari;
Mawatari, Shiro;
Fujino, Takehiko

Publication type:

Article

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.

Published in:

Neuropathology, 2014, v. 34, n. 3, p. 219, doi. 10.1111/neup.12081

By:

Miyata, Hajime;
Miyata, Mio;
Ohama, Eisaku

Publication type:

Article

Advanced age increases chromosome structural abnormalities in human spermatozoa.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 2, p. 145, doi. 10.1038/ejhg.2010.166

By:

Templado, Cristina;
Donate, Anna;
Giraldo, Jesús;
Bosch, Mercè;
Estop, Anna

Publication type:

Article

INSIGHT INTO HUMAN CONGENITAL ABNORMALITY.

Published in:

Reproductive Sciences, 2007, v. 14, n. 4, p. 295, doi. 10.1177/1933719107304304

By:

Maduro, Maria Rosa

Publication type:

Article

A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S24, doi. 10.1016/S1472-6483(10)62320-6

By:

Iourov, I. Y.;
Vorsanova, S. G.;
Liehr, T.;
Soloviev, I. V.;
Yurov, Y. B.

Publication type:

Article

Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.

Published in:

Clinical Genetics, 2019, v. 96, n. 5, p. 385, doi. 10.1111/cge.13602

By:

Sha, Yanwei;
Liu, Wensheng;
Wei, Xiaoli;
Zhu, Xingshen;
Luo, Xiangmin;
Liang, Lei;
Guo, Tonghang

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.

Published in:

Molecular Neurodegeneration, 2020, v. 15, n. 1, p. N.PAG, doi. 10.1186/s13024-020-00393-5

By:

Johnson, Erik C. B.;
Ho, Kaitlyn;
Yu, Gui-Qiu;
Das, Melanie;
Sanchez, Pascal E.;
Djukic, Biljana;
Lopez, Isabel;
Yu, Xinxing;
Gill, Michael;
Zhang, Weiping;
Paz, Jeanne T.;
Palop, Jorge J.;
Mucke, Lennart

Publication type:

Article

Comparison of unstimulated and stimulated behaviour in human fetuses with congenital abnormalities.

Published in:

1999

By:

Vindla, Srini;
James, David;
Sahota, Daljit;
Vindla, S;
James, D;
Sahota, D

Publication type:

journal article

Supplementary Pharmacotherapy for the Behavioral Abnormalities Caused by Stressors in Humans, Focused on Post-Traumatic Stress Disorder (PTSD).

Published in:

Journal of Clinical Medicine, 2023, v. 12, n. 4, p. 1680, doi. 10.3390/jcm12041680

By:

Fessel, Jeffrey

Publication type:

Article

Novel variants in TUBB8 gene cause multiple phenotypic abnormalities in human oocytes and early embryos.

Published in:

Journal of Ovarian Research, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13048-023-01274-3

By:

Hu, Tingwenyi;
Li, Chong;
Qiao, Sen;
Liu, Weiwei;
Han, Wei;
Li, Wei;
Shi, Rong;
Xue, Xia;
Shi, Juanzi;
Huang, Guoning;
Lin, Tingting

Publication type:

Article

Chromosome Abnormalities in the Human Oocyte.

Published in:

Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 107, doi. 10.1159/000323801

By:

Fragouli, E.;
Wells, D.;
Delhanty, J. D. A.

Publication type:

Article

C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome.

Published in:

Cytogenetic & Genome Research, 2006, v. 112, n. 1/2, p. 16, doi. 10.1159/000087509

By:

Rachidi, M.;
Lopes, C.;
Delezoide, A.-L.;
Delabar, J. M.

Publication type:

Article

Frequency and distribution of chromosome abnormalities in human oocytes.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 193, doi. 10.1159/000086889

By:

Kuliev, A.;
Cieslak, J.;
Verlinsky, Y.

Publication type:

Article

Frequency and distribution of chromosome abnormalities in human spermatozoa.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 199, doi. 10.1159/000086890

By:

Templado, C.;
Bosch, M.;
Benet, J.

Publication type:

Article

Natural Polyphenols May Normalize Hypochlorous Acid-Evoked Hemostatic Abnormalities in Human Blood.

Published in:

Antioxidants, 2022, v. 11, n. 4, p. N.PAG, doi. 10.3390/antiox11040779

By:

Misztal, Tomasz;
Golaszewska, Agata;
Marcińczyk, Natalia;
Tomasiak-Łozowska, Maria;
Szymanowska, Małgorzata;
Chabielska, Ewa;
Rusak, Tomasz

Publication type:

Article

Hyperglycemia-Induced Abnormalities in Rat and Human Corneas: The Potential of Second Harmonic Generation Microscopy.

Published in:

PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048388

By:

Latour, Gaël;
Kowalczuk, Laura;
Savoldelli, Michèle;
Bourges, Jean-Louis;
Plamann, Karsten;
Behar-Cohen, Francine;
Schanne-Klein, Marie-Claire

Publication type:

Article

Structural abnormalities in the human diaphragm in drowning and hanging deaths: preliminary results.

Published in:

Forensic Science, Medicine & Pathology, 2020, v. 16, n. 2, p. 265, doi. 10.1007/s12024-020-00235-2

By:

Girela-López, Eloy;
Beltran-Aroca, Cristina M;
Jimena, Ignacio;
Pérez-Jorge, Pablo;
Ramos-Medina, Valentin;
Ruz-Caracuel, Ignacio;
Gill, James R;
Peña-Amaro, Jose

Publication type:

Article

Chromosome Structural Alteration an Unusual Abnormality Characterizing Human Neoplasia.

Published in:

Novelty in Biomedicine, 2016, n. 2, p. 77

By:

Movafagh, Abolfazl;
Zare-Abdollahi, Davood;
Emamalizadeh, Babak;
Shahvaisizadeh, Farhad;
Mansouri, Neda;
Hashemi, Mehrdad;
Pour, Atefeh Heidary;
Heidari, Mohammad Hassan;
Tonekaboni, Seyed Hassan

Publication type:

Article

Chia (Salvia hispanica)-supplemented diet ameliorates non-alcoholic fatty liver disease and its metabolic abnormalities in humans.

Published in:

Lipids in Health & Disease, 2020, v. 19, n. 1, p. 1, doi. 10.1186/s12944-020-01283-x

By:

Medina-Urrutia, Aida;
Lopez-Uribe, Angel R.;
El Hafidi, Mohamed;
González-Salazar, Maria del Carmen;
Posadas-Sánchez, Rosalinda;
Jorge-Galarza, Esteban;
del Valle-Mondragón, Leonardo;
Juárez-Rojas, Juan G.

Publication type:

Article

The Impact of Acquired Genetic Abnormalities on the Clinical Translation of Human Pluripotent Stem Cells.

Published in:

Cells (2073-4409), 2021, v. 10, n. 11, p. 3246, doi. 10.3390/cells10113246

By:

Keller, Alexander;
Spits, Claudia

Publication type:

Article

The prevalence of liver abnormalities in humans due to Schistosoma japonicum by ultrasonography in China: a meta-analysis.

Published in:

2022

By:

Gu, Man-Man;
Sun, Meng-Tao;
Zhang, Jie-Ying;
Yu, Qiu-Fu;
Lu, Da-Bing

Publication type:

journal article

Meiotic errors in human oogenesis and spermatogenesis.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, n. 4, p. 523, doi. 10.1016/S1472-6483(10)60459-2

By:

Martin, Renée H.

Publication type:

Article

Trichorhinophalangeal syndrome type II associated with aplasia cutis congenita in a neonate.

Published in:

Pediatric Dermatology, 2022, v. 39, n. 3, p. 481, doi. 10.1111/pde.14934

By:

Tripodi, Giuseppe Daniele;
Dickerman, Deanna I.;
LeMosy, Ellen K.;
Davis, Loretta S.

Publication type:

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.

Published in:

Frontiers in Physiology, 2017, v. 8, p. 1, doi. 10.3389/fphys.2017.00278

By:

Britton, Oliver J.;
Bueno-Orovio, Alfonso;
Virág, László;
Varró, András

Publication type:

Article

Human Papillomavirus Infections in Women With and Without Squamous Cell Abnormalities of the Uterine Cervix.

Published in:

Scripta Medica, 2019, v. 50, n. 3, p. 69, doi. 10.5937/scriptamed50-21910

By:

Dabeski, Drage;
Dabeski, Ana;
Antovska, Vesna;
Trajanova, Milka;
Todorovska, Irena;
Sima, Aneta

Publication type:

Article

ABNORMAL APPEARANCES : INSPECTION, DISPLAY AND THE CLINIC.

Published in:

Medicina nei Secoli: Arte e Scienza, 2014, v. 26, n. 1, p. 333

By:

FEATHERSTONE, KATIE;
ATKINSON, PAUL

Publication type:

Article

Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 206, doi. 10.1159/000086891

By:

Pellestor, F.;
Anahory, T.;
Hamamah, S.

Publication type:

Article

Piezo2 expressed in proprioceptive neurons is essential for skeletal integrity.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16971-6

By:

Assaraf, Eran;
Blecher, Ronen;
Heinemann-Yerushalmi, Lia;
Krief, Sharon;
Carmel Vinestock, Ron;
Biton, Inbal E.;
Brumfeld, Vlad;
Rotkopf, Ron;
Avisar, Erez;
Agar, Gabriel;
Zelzer, Elazar

Publication type:

Article

Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals.

Published in:

PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005462

By:

Cloutier, Jeffrey M.;
Mahadevaiah, Shantha K.;
ElInati, Elias;
Nussenzweig, André;
Tóth, Attila;
Turner, James M. A.

Publication type:

Article

Research highlights.

Published in:

Nature Structural & Molecular Biology, 2008, v. 15, n. 10, p. 1006, doi. 10.1038/nsmb1008-1006

By:

Lall, Sabbi;
Montoya, Michelle;
Chen, Inês

Publication type:

Article

A review of computer vision-based approaches for physical rehabilitation and assessment.

Published in:

Multimedia Systems, 2022, v. 28, n. 1, p. 209, doi. 10.1007/s00530-021-00815-4

By:

Debnath, Bappaditya;
O'Brien, Mary;
Yamaguchi, Motonori;
Behera, Ardhendu

Publication type:

Article

Pedunculated Chiari 3 malformation with proatlas defect.

Published in:

2023

By:

Acharya, Abhijit;
Panigrahi, Souvagya;
Deo, Rama Chandra;
Senapati, Satya Bhusan;
Mahapatra, Ashok Kumar;
Samal, Rajiba Lochan

Publication type:

Case Study

Motion Sequence-Based Human Abnormality Detection Scheme for Smart Spaces.

Published in:

Wireless Personal Communications, 2011, v. 60, n. 3, p. 507, doi. 10.1007/s11277-011-0305-8

By:

Tak, Yoon-Sik;
Rho, Seungmin;
Hwang, Eenjun

Publication type:

Article

Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible Pathomechanisms.

Published in:

Antibiotics (2079-6382), 2023, v. 12, n. 6, p. 1029, doi. 10.3390/antibiotics12061029

By:

Ternák, Gábor;
Márovics, Gergely;
Sümegi, Katalin;
Bánfai, Zsolt;
Büki, Gergely;
Magyari, Lili;
Szabó, András;
Melegh, Béla

Publication type:

Article

The Role of Repeat DNA Sequences in Human Evolution and Disease.

Published in:: Journal of the Association of Genetic Technologists, 2022, v. 48, n. 2, p. 54
Publication type:: Article

Histology Atlas of the Developing Mouse Urinary System With Emphasis on Prenatal Days E10.5-E18.5.

Published in:

Toxicologic Pathology, 2019, v. 47, n. 7, p. 865, doi. 10.1177/0192623319873871

By:

Elmore, Susan A.;
Kavari, Sanam L.;
Hoenerhoff, Mark J.;
Mahler, Beth;
Scott, Brittany E.;
Yabe, Koichi;
Seely, John C.

Publication type:

Article

Inflammatory Effects and Regulatory Mechanisms of Chitinase-3-like-1 in Multiple Human Body Systems: A Comprehensive Review.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 24, p. 13437, doi. 10.3390/ijms252413437

By:

Liu, Dong;
Hu, Xin;
Ding, Xiao;
Li, Ming;
Ding, Lei

Publication type:

Article

Overlapping and Distinct Features of Cardiac Pathology in Inherited Human and Murine Ether Lipid Deficiency.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 1884, doi. 10.3390/ijms24031884

By:

Dorninger, Fabian;
Kiss, Attila;
Rothauer, Peter;
Stiglbauer-Tscholakoff, Alexander;
Kummer, Stefan;
Fallatah, Wedad;
Perera-Gonzalez, Mireia;
Hamza, Ouafa;
König, Theresa;
Bober, Michael B.;
Cavallé-Garrido, Tiscar;
Braverman, Nancy E.;
Forss-Petter, Sonja;
Pifl, Christian;
Bauer, Jan;
Bittner, Reginald E.;
Helbich, Thomas H.;
Podesser, Bruno K.;
Todt, Hannes;
Berger, Johannes

Publication type:

Article

Honeycomb sterna: an unusual case of a developmental abnormality in the sternum.

Published in:

Surgical & Radiologic Anatomy, 2020, v. 42, n. 1, p. 91, doi. 10.1007/s00276-019-02350-4

By:

Hirst, Cara Stella;
White, S.;
Siek, T.;
Gasparik, A.

Publication type:

Article

Molecular mechanisms of MHC class I abnormalities and APM components in human tumors.

Published in:

Cancer Immunology, Immunotherapy, 2008, v. 57, n. 11, p. 1719, doi. 10.1007/s00262-008-0515-4

By:

Seliger, Barbara

Publication type:

Article

Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitation.

Published in:

1991

By:

Benet, J.;
Navarro, J.;
Genescà, A.;
Egozcue, J.;
Templado, C.

Publication type:

journal article

Free as a BRD4: Bromodomain Inhibition Ameliorates Disease Phenotypes in a Model of MECP2 Deficiency and Is a Potential Therapy for Rett Syndrome.

Published in:

Epilepsy Currents, 2020, v. 20, n. 6, p. 390, doi. 10.1177/1535759720960469

By:

Lamar, Kay-Marie Joan;
Carvill, Gemma L.

Publication type:

Article

Prevalence of human papillomavirus genotypes in cytologic abnormalities from unvaccinated women living in north-western Spain.

Published in:

APMIS, 2011, v. 119, n. 3, p. 204, doi. 10.1111/j.1600-0463.2010.02711.x

By:

OTERO-MOTTA, ANA PASTORA;
ORDÓÑEZ, JOSÉ LUIS;
GONZÁ'LEZ-CELADOR, RAFAEL;
RIVAS, BELEN;
MACÍAS, MARÍA DEL CARMEN GARCÍA;
BULLON, AGUSTIN;
ABAD, MARÍA DEL MAR

Publication type:

Article