Search Results - "microarray"

Antibody repertoire profiling with mimotope arrays by Shina Pashova, Christoph Schneider, Stephan von Gunten, Anastas Pashov

Connect to this object online.

An Indole-2-Carboxamide Derivative, LG4, Alleviates Diabetic Kidney Disease Through Inhibiting MAPK-Mediated Inflammatory Responses by Qian J, Yin S, Ye L, Wang Z, Shu S, Mou Z, Xu M, Chattipakorn N, Liu Z, Liang G

Connect to this object online.

Up-Regulated Expression of ICAM1, MT1A, PTGS2, LCE3D, PPARD, and GM-CSF2 Following Solar Skincare Protection and Repair Strategies in a 3-Dimensional Reconstructed Human Skin Model by Tanaka Y, Parker R, Aganahi A

Connect to this object online.

MiR-132 controls pancreatic beta cell proliferation and survival through Pten/Akt/Foxo3 signaling by Hassan Mziaut, Georg Henniger, Katharina Ganss, Sebastian Hempel, Steffen Wolk, Johanna McChord, Kamal Chowdhury, Philippe Ravassard, Klaus-Peter Knoch, Christian Krautz, Jürgen Weitz, Robert Grützmann, Christian Pilarsky, Michele Solimena, Stephan Kersting

Connect to this object online.

A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women by Yoo HY, Lee KC, Woo JE, Park SH, Lee S, Joo J, Bae JS, Kwon HJ, Park BJ

Connect to this object online.

INVESTIGATING UNIVERSITY STUDENT'S ACCEPTANCE OF VIRTUAL AND REMOTE LABS IN THEIR LEARNING by Nanda Eska Anugrah Nasution, Chairany Rizka

Connect to this object online.

A Novel 2.3 Mb Microduplication of 9q34.3 Inserted into 19q13.4 in a Patient with Learning Disabilities by Shalinder Singh, Fern Ashton, Renate Marquis-Nicholson, Jennifer M. Love, Chuan-Ching Lan, Salim Aftimos, Alice M. George, Donald R. Love

Connect to this object online.

"Idiopathic" mental retardation and new chromosomal abnormalities by El-Malhany Nadia, Lo-Castro Adriana, Galasso Cinzia, Curatolo Paolo

Connect to this object online.

A Rare Interstitial Duplication of 8q22.1-8q24.3 Associated with Syndromic Bilateral Cleft Lip/Palate by Regina Ferreira Rezek, Ana Angélica Rodrigues Abbas, Juliana Forte Mazzeu, Siliana Maria Duarte Miranda, Cibele Velloso-Rodrigues

Connect to this object online.

Involved and Uninvolved Psoriatic Keratinocytes Display a Resistance to Apoptosis that may Contribute to Epidermal Thickness by Cecilia Bivik Eding, Charlotta Enerbäck

Connect to this object online.

Autism spectrum disorder with microdeletion 10q26 by subtelomere FISH by Tonk VS, Wilson GN

Connect to this object online.

Genomic expression in non syndromic cleft lip and palate patients: A review by D. Mehrotra

Connect to this object online.

Polymer Delivery Systems for Long-Acting Antiretroviral Drugs by Mohammad Ullah Nayan, Sudipta Panja, Ashrafi Sultana, Lubaba A. Zaman, Lalitkumar K. Vora, Brady Sillman, Howard E. Gendelman, Benson Edagwa

Connect to this object online.

Dissolving Microneedles Developed in Association with Nanosystems: A Scoping Review on the Quality Parameters of These Emerging Systems for Drug or Protein Transdermal Delivery by Patrícia Weimer, Rochele Cassanta Rossi, Letícia Scherer Koester

Connect to this object online.

Integration of Transcriptomics and Metabolomics to Reveal the Molecular Mechanisms Underlying Rhodium Nanoparticles-Based Photodynamic Cancer Therapy by Andres Machuca, Estefania Garcia-Calvo, Daniela S. Anunciação, Jose L. Luque-Garcia

Connect to this object online.

GENETIC APPROACH IN THE DIAGNOSIS OF CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT by Katja Jarc Georgiev, Matjaž Kopač, Sara Bertok

Connect to this object online.

Prenatally diagnosed microdeletion in the TCOF1 gene in fetal congenital primary Treacher Collins Syndrome by Wei Shin Chou, Jia Shing Chen, Yu Ming Shiao, Ju Chin Tsauer, Yi Fen Chang, Ching Hua Hsiao

Connect to this object online.

OMICS Approaches Evaluating Keloid and Hypertrophic Scars by Nazihah Bakhtyar, Saeid Amini-Nik, Marc G. Jeschke

Connect to this object online.

Congenital second-degree heart block and total anomalous pulmonary venous return associated with microduplication of 1q32.2 by Surasak Puvabanditsin, Vidya Puthenpura, Seyni Gueye-Ndiaye, Michele Takyi, Adaora Madubuko, Lauren Walzer, Rajeev Mehta

Connect to this object online.

Monosomy 3pter-p25.3 and Trisomy 1q42.13-qter in a Boy With Profound Growth and Developmental Restriction, Multiple Congenital Anomalies, and Early Death by Chumei Li, Vikas Mahajan, Jia-Chi Wang, Bosco Paes

Connect to this object online.