Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemia

Por Thomas, Ellen R A, Atanur, Santosh S, Norsworthy, Penny J, Encheva, Vesela, Snijders, Ambrosius P, Game, Laurence, Vandrovcova, Jana, Siddiq, Afshan, Seed, Mary, Soutar, Anne K, Aitman, Timothy J
Publicado em 2013

Clinically relevant fluoroquinolone resistance due to constitutive overexpression of the PatAB ABC...

Por Baylay, Alison J., Piddock, Laura J. V.
Publicado no J Antimicrob Chemother (2015)

Novel Device to Trend Impedance and Fluorescence of the Cervix for Preterm Birth Detection

Por Etemadi, Mozziyar, Chung, Philip, Heller, J. Alex, Liu, Jonathan, Grossman-Kahn, Rebecca, Rand, Larry, Roy, Shuvo
Publicado no Conf Proc IEEE Eng Med Biol Soc (2013)

The molecular basis of homocystinuria due to cystathionine beta-synthase deficiency in Italian families, and report of four novel mutations.

Por Sebastio, G, Sperandeo, M P, Panico, M, de Franchis, R, Kraus, J P, Andria, G
Publicado em 1995

Defining the Etiology of Diarrhea: Novel Approaches

Por Operario, Darwin J., Houpt, Eric
Publicado em 2011

A Novel Rat Model of Hereditary Hemochromatosis Due to a Mutation in Transferrin Receptor 2

Por Bartnikas, Thomas B, Wildt, Sheryl J, Wineinger, Amy E, Schmitz-Abe, Klaus, Markianos, Kyriacos, Cooper, Dale M, Fleming, Mark D
Publicado em 2013

A novel, species-specific, real-time PCR assay for the detection of the emerging zoonotic parasite Ancylostoma ceylanicum in human stool

Por Papaiakovou, Marina, Pilotte, Nils, Grant, Jessica R., Traub, Rebecca J., Llewellyn, Stacey, McCarthy, James S., Krolewiecki, Alejandro J., Cimino, Rubén, Mejia, Rojelio, Williams, Steven A.
Publicado no PLoS Negl Trop Dis (2017)

Identification and Characterization of 40 Novel Hydroxymethylbilane Synthase Mutations that Cause Acute Intermittent Porphyria

Por Chen, Brenden, Solis-Villa, Constanza, Erwin, Angelika L., Balwani, Manisha, Nazrenko, Irina, Phillips, John D., Desnick, Robert J., Yasuda, Makiko
Publicado no J Inherit Metab Dis (2019)

Hippocampal Evoked Potentials in Novel Environments: A Behavioral Clamping Method

Por Wu, Ying, Sutherland, Robert J.
Publicado em 2006

A novel molecular toolkit for rapid detection of the pathogen and primary vector of thousand cankers disease

Por Oren, Emel, Klingeman, William, Gazis, Romina, Moulton, John, Lambdin, Paris, Coggeshall, Mark, Hulcr, Jiri, Seybold, Steven J., Hadziabdic, Denita
Publicado no PLoS One (2018)

Rapid detection of haemotropic mycoplasma infection of feline erythrocytes using a novel flow cytometric approach

Por Sánchez-Pérez, Angeles, Brown, Graeme, Malik, Richard, Assinder, Stephen J, Cantlon, Katherine, Gotsis, Christine, Dunbar, Samantha, Fraser, Stuart T
Publicado em 2013

Human RNA “Rumor” Viruses: the Search for Novel Human Retroviruses in Chronic Disease

Por Voisset, Cécile, Weiss, Robin A., Griffiths, David J.
Publicado em 2008

Identification of Novel Compounds That Increase SMN Protein Levels Using an Improved SMN2 Reporter Cell Assay

Por Cherry, Jonathan J., Evans, Matthew C., Ni, Jake, Cuny, Gregory D., Glicksman, Marcie A., Androphy, Elliot J.
Publicado em 2012

A novel multiplex PCR for detection of Pseudomonas aeruginosa: A major cause of wound infections

Por Salman, Muhammad, Ali, Aamir, Haque, Abdul
Publicado em 2013

Tracking type specific prevalence of human Papillomavirus in cervical pre-cancer: a novel sampling strategy

Por Waters, Edward K, Kaldor, John, Hamilton, Andrew J, Smith, Anthony MA, Philp, David J, Donovan, Basil, Regan, David G
Publicado em 2012

ABO exon and intron analysis in individuals with the A(weak)B phenotype reveals a novel O(1v)-A(2...

Por Hosseini-Maaf, Bahram, Hellberg, Åsa, Rodrigues, Maria J, Chester, M Alan, Olsson, Martin L
Publicado em 2003

Novel Syntrophic Populations Dominate an Ammonia-Tolerant Methanogenic Microbiome

Por Frank, J. A., Arntzen, M. Ø., Sun, L., Hagen, L. H., McHardy, A. C., Horn, S. J., Eijsink, V. G. H., Schnürer, A., Pope, P. B.
Publicado no mSystems (2016)

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Por Paulussen, Aimee D C, Steyls, Anja, Vanoevelen, Jo, van Tienen, Florence HJ, Krapels, Ingrid P C, Claes, Godelieve RF, Chocron, Sonja, Velter, Crool, Tan-Sindhunata, Gita M, Lundin, Catarina, Valenzuela, Irene, Nagy, Balint, Bache, Iben, Maroun, Lisa Leth, Avela, Kristiina, Brunner, Han G, Smeets, Hubert J M, Bakkers, Jeroen, van den Wijngaard, Arthur
Publicado no Eur J Hum Genet (2016)

Novel tailoring algorithm for abrupt motion artifact removal in photoplethysmogram signals

Por Pu, Limeng, Chacon, Pedro J., Wu, Hsiao-Chun, Choi, Jin-Woo
Publicado no Biomed Eng Lett (2017)

Clinical validation of a next-generation sequencing-based multi-cancer early detection "liquid...

Por Andi Flory, Kristina M Kruglyak, John A Tynan, Lisa M McLennan, Jill M Rafalko, Patrick Christian Fiaux, Gilberto E Hernandez, Francesco Marass, Prachi Nakashe, Carlos A Ruiz-Perez, Donna M Fath, Thuy Jennings, Rita Motalli-Pepio, Kate Wotrang, Angela L McCleary-Wheeler, Susan Lana, Brenda Phillips, Brian K Flesner, Nicole F Leibman, Tracy LaDue, Chelsea D Tripp, Brenda L Coomber, J Paul Woods, Mairin Miller, Sean W Aiken, Amber Wolf-Ringwall, Antonella Borgatti, Kathleen Kraska, Christopher B Thomson, Alane Kosanovich Cahalane, Rebecca L Murray, William C Kisseberth, Maria A Camps-Palau, Franck Floch, Claire Beaudu-Lange, Aurélia Klajer-Peres, Olivier Keravel, Luc-André Fribourg-Blanc, Pascale Chicha Mazetier, Angelo Marco, Molly B McLeod, Erin Portillo, Terry S Clark, Scott Judd, C Kirk Feinberg, Marie Benitez, Candace Runyan, Lindsey Hackett, Scott Lafey, Danielle Richardson, Sarah Vineyard, Mary Tefend Campbell, Nilesh Dharajiya, Taylor J Jensen, Dirk van den Boom, Luis A Diaz, Daniel S Grosu, Arthur Polk, Kalle Marsal, Susan Cho Hicks, Katherine M Lytle, Lauren Holtvoigt, Jason Chibuk, Ilya Chorny, Dana W Y Tsui
Publicado em 2022-01-01