Zoekresultaten - "phenotyping"

A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal) door Joana Rosa, Patrícia Gaspar-Silva, Paula Pacheco, Conceição Silva, Cláudia C. Branco, Barbara S. Vieira, Alexandra Carreiro, Juan Gonçalves, Luisa Mota-Vieira

Connect to this object online.

NOX1 and NOX2: Two enzymes that promote endothelial-to-mesenchymal transition induced by melanoma conditioned media door Valentin Platel, Diane Lechevalier, Clara Bourreau, Sarah Renault, Ivana Šoborová, Caroline Jeannière, Ludovic Martin, Olivier Hérault, Isabelle Corre, Nicolas Clere

Connect to this object online.

CARDIORENAL INTERACTION IN DECOMPENSATED CHRONIC HEART FAILURE door Zh. D. Kobalava, S. V. Villevalde, M. A. Efremovtseva

Connect to this object online.

Host genetic variability and pneumococcal disease: a systematic review and meta-analysis door Anne T. Kloek, Matthijs C. Brouwer, Diederik van de Beek

Connect to this object online.

Pathway-targeted pharmacogenomics of CYP1A2 in human liver door Kathrin eKlein, Stefan eWinter, Miia eTurpeinen, Matthias eSchwab, Matthias eSchwab, Ulrich M Zanger

Connect to this object online.

LGR5 expression and clinicopathological features of the invasive front in the fat infiltration area of pancreatic cancer door Masato Kamakura, Takeshi Uehara, Mai Iwaya, Shiho Asaka, Shota Kobayashi, Tomoyuki Nakajima, Yasuhiro Kinugawa, Tadanobu Nagaya, Takahiro Yoshizawa, Akira Shimizu, Hiroyoshi Ota, Takeji Umemura

Connect to this object online.

Impaired remodeling phase of fracture repair in the absence of matrix metalloproteinase-2 door Shirley Lieu, Erik Hansen, Russell Dedini, Danielle Behonick, Zena Werb, Theodore Miclau, Ralph Marcucio, Céline Colnot

Connect to this object online.

GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation door Roozbeh Manshaei, Sean DeLong, Veronica Andric, Esha Joshi, John B. A. Okello, Priya Dhir, Cherith Somerville, Kirsten M. Farncombe, Kelsey Kalbfleisch, Rebekah K. Jobling, Stephen W. Scherer, Raymond H. Kim, S. Mohsen Hosseini

Connect to this object online.

Vitamin D status contributes to the antimicrobial activity of macrophages against Mycobacterium leprae. door Elliot W Kim, Rosane M B Teles, Salem Haile, Philip T Liu, Robert L Modlin

Connect to this object online.

Clinical and Genetic Spectrum of Encephalopathy in the Korean Pediatric Population door Woo Joong Kim, Young Kyu Shim, Young Jun Ko, Soo Yeon Kim, Hunmin Kim, Byung Chan Lim, Hee Hwang, Jieun Choi, Ki Joong Kim, Jong-Hee Chae

Connect to this object online.

HYPERTRIGLYCERIDEMIC WAIST AND ASSOCIATED FACTORS IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS door Lílian Caroline de Souza e Silva, Skalyt Lee Barbosa e Silva, Ávilla Monalisa Silva de Oliveira, Jacqueline Rosangela de Araujo, Ilma Kruze Grande de Arruda, Regiane Maio, Maria da Conceição Chaves de Lemos

Connect to this object online.

Long-term treatment for endometriosis with dienogest: efficacy, side effects and tolerability door Francesco La Torre, Silvia Vannuccini, Federico Toscano, Ernesto Gallucci, Gretha Orlandi, Virginia Manzi, Felice Petraglia

Connect to this object online.

The genetic and molecular basis of O-antigenic diversity in Burkholderia pseudomallei lipopolysaccharide. door Apichai Tuanyok, Joshua K Stone, Mark Mayo, Mirjam Kaestli, Jeffrey Gruendike, Shalamar Georgia, Stephanie Warrington, Travis Mullins, Christopher J Allender, David M Wagner, Narisara Chantratita, Sharon J Peacock, Bart J Currie, Paul Keim

Connect to this object online.

A novel nonsense ATP2C1 mutation causes Hailey-Hailey disease in a Tunisian family door Marwa Chourabi, Dorra H'mida-Ben Brahim, Carine Bonnard, Amina Aounallah, Alvin Yu Ng, Sumanty Tohari, Byrappa Venkatesh, Ali Saad, Lobna Boussofara, Bruno Reversade, Mohamed Denguezli

Connect to this object online.

Preclinical research in Rett syndrome: setting the foundation for translational success door David M. Katz, Joanne E. Berger-Sweeney, James H. Eubanks, Monica J. Justice, Jeffrey L. Neul, Lucas Pozzo-Miller, Mary E. Blue, Diana Christian, Jacqueline N. Crawley, Maurizio Giustetto, Jacky Guy, C. James Howell, Miriam Kron, Sacha B. Nelson, Rodney C. Samaco, Laura R. Schaevitz, Coryse St. Hillaire-Clarke, Juan L. Young, Huda Y. Zoghbi, Laura A. Mamounas

Connect to this object online.

Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction door Barrett J. Burger, Shannon Rose, Shannon Rose, Sirish C. Bennuri, Sirish C. Bennuri, Pritmohinder S. Gill, Marie L. Tippett, Marie L. Tippett, Leanna Delhey, Leanna Delhey, Stepan Melnyk, Stepan Melnyk, Richard E. Frye, Richard E. Frye

Connect to this object online.

A Pathogenic Missense Variant (c.1617G>A, p.Met539Ile) in UBA1 Causing Infantile X-Linked Spinal Muscular Atrophy (SMAX2) door Xin Hua Wang, Lin Mei Zhang, Xue Yang, Shui Zhen Zhou

Connect to this object online.

Features of Cellular Link of Immune Response in School-Age Children with Late-Onset Asthma Depending on Acetylation Polymorphism door U.I. Marusyk, I.U. Bezrukov

Connect to this object online.

The role of Staphylococcus aureus quorum sensing in cutaneous and systemic infections door Yuriko Yamazaki, Tomoka Ito, Masakazu Tamai, Seitaro Nakagawa, Yuumi Nakamura

Connect to this object online.

Intrauterine IPEX door Magda Carneiro-Sampaio, Carlos Alberto Moreira-Filho, Silvia Yumi Bando, Jocelyne Demengeot, Antonio Coutinho

Connect to this object online.