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FHL1 Reduces Dystrophy in Transgenic Mice Overexpressing FSHD Muscular Dystrophy Region Gene 1 (FRG1).
Published in:
PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0117665
By:
- Feeney, Sandra J.;
- McGrath, Meagan J.;
- Sriratana, Absorn;
- Gehrig, Stefan M.;
- Lynch, Gordon S.;
- D’Arcy, Colleen E.;
- Price, John T.;
- McLean, Catriona A.;
- Tupler, Rossella;
- Mitchell, Christina A.
Publication type:
Article
Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis.
Published in:
2001
By:
- Feeney, Sandra J.;
- McKelvie, Penelope A.;
- Austin, Lawrence;
- Jean-Francois, M.J. Bernadette;
- Kapsa, Robert;
- Tombs, Stefania M.;
- Byrne, Edward;
- Feeney, S J;
- McKelvie, P A;
- Austin, L;
- Jean-Francois, M J;
- Kapsa, R;
- Tombs, S M;
- Byrne, E
Publication type:
journal article
Evaluation of ICA512As in combination with other islet cell autoantibodies at the onset of IDDM.
Published in:
1997
By:
- Feeney, Sandra J.;
- Myers, Mark A.;
- Mackay, Ian R.;
- Zimmet, Paul Z.;
- Howard, Neville;
- Verge, Charles F.;
- Rowley, Merrill J.;
- Feeney, S J;
- Myers, M A;
- Mackay, I R;
- Zimmet, P Z;
- Howard, N;
- Verge, C F;
- Rowley, M J
Publication type:
journal article
Defective lysosome reformation during autophagy causes skeletal muscle disease.
Published in:
2021
By:
- McGrath, Meagan J.;
- Eramo, Matthew J.;
- Gurung, Rajendra;
- Sriratana, Absorn;
- Gehrig, Stefan M.;
- Lynch, Gordon S.;
- Lourdes, Sonia Raveena;
- Koentgen, Frank;
- Feeney, Sandra J.;
- Lazarou, Michael;
- McLean, Catriona A.;
- Mitchell, Christina A.
Publication type:
journal article
β-catenin ablation exacerbates polycystic kidney disease progression.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 2, p. 230, doi. 10.1093/hmg/ddy309
By:
- Conduit, Sarah E;
- Hakim, Sandra;
- Feeney, Sandra J;
- Ooms, Lisa M;
- Dyson, Jennifer M;
- Abud, Helen E;
- Mitchell, Christina A
Publication type:
Article
Inpp5e suppresses polycystic kidney disease via inhibition of PI3K/Akt-dependent mTORC1 signaling.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 11, p. 2295, doi. 10.1093/hmg/ddw097
By:
- Hakim, Sandra;
- Dyson, Jennifer M.;
- Feeney, Sandra J.;
- Davies, Elizabeth M.;
- Sriratana, Absorn;
- Koenig, Monica N.;
- Plotnikova, Olga V.;
- Smyth, Ian M.;
- Ricardo, Sharon D.;
- Hobbs, Robin M.;
- Mitchell, Christina A.
Publication type:
Article
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 3, p. 618, doi. 10.1093/hmg/ddt449
By:
- D'Arcy, Colleen E.;
- Feeney, Sandra J.;
- McLean, Catriona A.;
- Gehrig, Stefan M.;
- Lynch, Gordon S.;
- Smith, Jaclyn E.;
- Cowling, Belinda S.;
- Mitchell, Christina A.;
- McGrath, Meagan J.
Publication type:
Article

Found: 7

FHL1 Reduces Dystrophy in Transgenic Mice Overexpressing FSHD Muscular Dystrophy Region Gene 1 (FRG1).

Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis.

Evaluation of ICA512As in combination with other islet cell autoantibodies at the onset of IDDM.

Defective lysosome reformation during autophagy causes skeletal muscle disease.

β-catenin ablation exacerbates polycystic kidney disease progression.

Inpp5e suppresses polycystic kidney disease via inhibition of PI3K/Akt-dependent mTORC1 signaling.

Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.