Хайлтын үр дүнгүүд - Chen, Ke‐Lian

Nucleocytoplasmic transport defect in a North American patient with ALS8 -н Guber, Robert D., Schindler, Alice B., Budron, Maher S., Chen, Ke‐lian, Li, Yuebing, Fischbeck, Kenneth H., Grunseich, Christopher

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Systemic Delivery of MicroRNA Using Recombinant Adeno-associated Virus Serotype 9 to Treat Neuromuscular Diseases in Rodents -н Pourshafie, Naemeh, Lee, Philip R., Chen, Ke-lian, Harmison, George G., Bott, Laura C., Fischbeck, Kenneth H., Rinaldi, Carlo

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Insulinlike Growth Factor (IGF)-1 Administration Ameliorates Disease Manifestations in a Mouse Model of Spinal and Bulbar Muscular Atrophy -н Rinaldi, Carlo, Bott, Laura C, Chen, Ke-lian, Harmison, George G, Katsuno, Masahisa, Sobue, Gen, Pennuto, Maria, Fischbeck, Kenneth H

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

MiR-298 Counteracts Mutant Androgen Receptor Toxicity in Spinal and Bulbar Muscular Atrophy -н Pourshafie, Naemeh, Lee, Philip R, Chen, Ke-lian, Harmison, George G, Bott, Laura C, Katsuno, Masahisa, Sobue, Gen, Burnett, Barrington G, Fischbeck, Kenneth H, Rinaldi, Carlo

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Stem cell-derived motor neurons from spinal and bulbar muscular atrophy patients -н Grunseich, Christopher, Zukosky, Kristen, Kats, Ilona R., Ghosh, Laboni, Harmison, George G., Bott, Laura C., Rinaldi, Carlo, Chen, Ke-lian, Chen, Guibin, Boehm, Manfred, Fischbeck, Kenneth H.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Peripheral neuropathy in a family with Sandhoff disease and SH3TC2 deficiency -н Grunseich, Christopher, Schindler, Alice B., Chen, Ke-lian, Bakar, Dara, Mankodi, Ami, Traslavina, Ryan, Ray-Chaudhury, Abhik, Lehky, Tanya J., Baker, Eva H., Maragakis, Nicholas J., Tifft, Cynthia J., Fischbeck, Kenneth H.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy -н Bott, Laura C., Badders, Nisha M., Chen, Ke-lian, Harmison, George G., Bautista, Elaine, Shih, Charles C.-Y., Katsuno, Masahisa, Sobue, Gen, Taylor, J. Paul, Dantuma, Nico P., Fischbeck, Kenneth H., Rinaldi, Carlo

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss -н Guinto, Cheick O., Diarra, Salimata, Diallo, Salimata, Cissé, Lassana, Coulibaly, Thomas, Diallo, Seybou H., Taméga, Abdoulaye, Chen, Ke‐Lian, Schindler, Alice B., Bagayoko, Koumba, Simaga, Assiatou, Blackstone, Craig, Fischbeck, Kenneth H., Landouré, Guida

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat -н Grunseich, Christopher, Kats, Ilona R., Bott, Laura C., Rinaldi, Carlo, Kokkinis, Angela, Fox, Derrick, Chen, Ke-lian, Schindler, Alice B., Mankodi, Ami K., Shrader, Joseph A., Schwartz, Daniel P., Lehky, Tanya J., Liu, Chia-Ying, Fischbeck, Kenneth H.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia -н Rinaldi, Carlo, Schmidt, Thomas, Situ, Alan J., Johnson, Janel O., Lee, Philip R., Chen, Ke-lian, Bott, Laura C., Fadó, Rut, Harmison, George H., Parodi, Sara, Grunseich, Christopher, Renvoisé, Benoît, Biesecker, Leslie G., De Michele, Giuseppe, Santorelli, Filippo M., Filla, Alessandro, Stevanin, Giovanni, Dürr, Alexandra, Brice, Alexis, Casals, Núria, Traynor, Bryan J., Blackstone, Craig, Ulmer, Tobias S., Fischbeck, Kenneth H.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах