Resultados da busca - Kara E. Boodhansingh
- Mostrando 1 - 6 resultados de 6
-
1
Pharmacological Correction of Trafficking Defects in ATP-sensitive Potassium Channels Caused by Sulfonylurea Receptor 1 Mutations por Gregory Martin, Emily A. Rex, Prasanna K. Devaraneni, Jerod S. Denton, Kara E. Boodhansingh, Diva D. De León, Charles A. Stanley, Show‐Ling Shyng
Publicado em 2016Artigo -
2
Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2 por Christine T. Ferrara, Kara E. Boodhansingh, Eleonora Paradies, Giuseppe Fiermonte, Linda Steinkrauss, Lisa Swartz Topor, Jose Bernardo Quintos, Arupa Ganguly, Diva D. De León, Ferdinando Palmieri, Charles A. Stanley
Publicado em 2016Artigo -
3
Congenital Hyperinsulinism in Infants with Turner Syndrome: Possible Association with Monosomy X and <b><i>KDM6A</i></b> Haploinsufficiency por C. E. Gibson, Kara E. Boodhansingh, Changhong Li, Laura K. Conlin, Pan Chen, Susan Becker, Tricia R. Bhatti, Vaneeta Bamba, N. Scott Adzick, Diva D. De León, Arupa Ganguly, Charles A. Stanley
Publicado em 2018Artigo -
4
Dominant Form of Congenital Hyperinsulinism Maps to HK1 Region on 10q por Sara E. Pinney, Karthik Ganapathy, Jonathan P. Bradfield, David Stokes, Ariella Sasson, Katarzyna Mackiewicz, Kara E. Boodhansingh, Nkecha Hughes, Susan Becker, Stephanie Givler, Courtney MacMullen, Dimitrios Monos, Arupa Ganguly, Hákon Hákonarson, Charles A. Stanley
Publicado em 2013Artigo -
5
Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome por Jennifer M. Kalish, Kara E. Boodhansingh, Tricia R. Bhatti, Arupa Ganguly, Laura K. Conlin, Susan Becker, Stephanie Givler, Lindsey Mighion, Andrew Palladino, N. Scott Adzick, Diva D. De León, Charles A. Stanley, Matthew A. Deardorff
Publicado em 2015Artigo -
6
Functional and Metabolomic Consequences of KATP Channel Inactivation in Human Islets por Changhong Li, Amanda M. Ackermann, Kara E. Boodhansingh, Tricia R. Bhatti, Chengyang Liu, Jonathan Schug, Nicolai M. Doliba, Bing Han, Karen E. Cosgrove, Indraneel Banerjee, Franz M. Matschinsky, Itzhak Nissim, Klaus H. Kaestner, Ali Naji, N. Scott Adzick, Mark J. Dunne, Charles A. Stanley, Diva D. De León
Publicado em 2017Artigo
Ferramentas de busca:
Assuntos relacionados
Biology
Hyperinsulinism
Insulin resistance
Congenital hyperinsulinism
Diazoxide
Endocrinology
Gene
Insulin
Genetics
Internal medicine
Medicine
Phenotype
Biochemistry
Chromosome
Hypoglycemia
Karyotype
Missense mutation
Mutation
ATP-sensitive potassium channel
Alanine
Amino acid
Beckwith–Wiedemann syndrome
Biophysics
CHOP
Candidate gene
Carbohydrate metabolism
Cell biology
Chemistry
Chemotherapy
DNA methylation