|
"mcgrath j a"的相关文件
显示项目 1-10 / 22 (共3页)
1 2 3 > >>
每页显示[10|25|50]项目
| 國立成功大學 |
2023 |
Atrichia with papular lesions in a 1-year-old girl resulting from a new homozygous nonsense pathogenic variant in the hairless gene
|
Segovia, J.-C.;Lin, Y.-C.;Aala, W.;Dolendo, M.C.J.;McGrath, J.A.;Hsu, C.-K.;Guevara, B.E.K. |
| 國立成功大學 |
2023 |
Loss of RhoE Function in Dermatofibroma Promotes Disorganized Dermal Fibroblast Extracellular Matrix and Increased Integrin Activation
|
Endzhievskaya, S.;Hsu, C.-K.;Yang, H.-S.;Huang, Huang H.-Y.;Lin, Y.-C.;Hong, Y.-K.;Lee, J.Y.W.;Onoufriadis, A.;Takeichi, Takeichi T.;Yu-Yun, Lee J.;Shaw, T.J.;McGrath, J.A.;Parsons, M. |
| 國立成功大學 |
2022 |
Transcriptomic Analysis of Blaschko-Linear Psoriasis Reveals Shared and Distinct Features with Psoriasis Vulgaris
|
Onoufriadis, A.;Niazi, U.;Dimitrakopoulou, K.;Reich, J.;Ainali, C.;Papanikolaou, M.;Kesidou, E.;Hsu, C.-K.;Saqi, M.;McGrath, J.A.;Reich, K. |
| 國立成功大學 |
2022 |
Plasma metabolomic and lipidomic profiling highlights metabolic changes in keloid-prone individuals
|
Onoufriadis, A.;Hsu, C.-K.;Hong, Y.-K.;Lin, Y.-C.;McGrath, J.A. |
| 臺大學術典藏 |
2021-07-06T02:04:17Z |
Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
|
PEI-LUNG CHEN; Avramopoulos D.; Lasseter V.K.; McGrath J.A.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Feng N.; Steel G.; Cutting A.S.; Wolyniec P.; Pulver A.E.; Valle D. |
| 臺大學術典藏 |
2021-07-06T02:04:17Z |
Familiality of novel factorial dimensions of schizophrenia
|
McGrath J.A.; Avramopoulos D.; Lasseter V.K.; Wolyniec P.S.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Thornquist M.H.; Luke J.R.; PEI-LUNG CHEN; Valle D.; Pulver A.E. |
| 臺大學術典藏 |
2021-07-06T02:04:10Z |
Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling
|
Liu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D. |
| 國立成功大學 |
2021 |
Current topics in Epidermolysis bullosa: Pathophysiology and therapeutic challenges
|
Natsuga, K.;Shinkuma, Shinkuma S.;Hsu, C.-K.;Fujita, Y.;Ishiko, A.;Tamai, K.;McGrath, J.A. |
| 國立成功大學 |
2021 |
A germline mutation in the platelet-derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosis
|
Onoufriadis, A.;Boulouadnine, Boulouadnine B.;Dachy, G.;Higashino, T.;Huang, Huang H.Y.;Hsu, C.K.;Simpson, M.A.;Bork, K.;Demoulin, J.B.;McGrath, J.A. |
| 國立成功大學 |
2020 |
Plectin missense mutation p.Leu319pro in the pathogenesis of autosomal recessive epidermolysis bullosa simplex
|
Tu, W.-T.;Chen, P.-C.;Hou, P.-C.;Huang, Huang H.-Y.;Wang, J.-Y.;Chao, S.-C.;Lee, J.Y.-Y.;McGrath, J.A.;Natsuga, K.;Hsu, C.-K. |
显示项目 1-10 / 22 (共3页)
1 2 3 > >>
每页显示[10|25|50]项目
|
