Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa, JF O'Toole… - Nature …, 2007 - nature.com
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …
被引用次数：269 相关文章

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut… - Nature …, 2007 - utsouthwestern.elsevierpure.com
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …
[PDF] researchgate.net

[PDF][PDF] Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa, JF O'Toole… - researchgate.net
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa… - Nature …, 2007 - eprints.ncl.ac.uk
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …

[引用][C] Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa, JF O'Toole… - Nature Genetics, 2007 - cir.nii.ac.jp
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and
fibrosis | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa… - Nature …, 2007 - pubmed.ncbi.nlm.nih.gov
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M Attanasio, NH Uhlenhaut, VH Sousa, JF O'Toole… - Nature …, 2007 - go.gale.com
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.

M Attanasio, NH Uhlenhaut, VH Sousa, JF O'Toole… - Nature …, 2007 - europepmc.org
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …

[引用][C] Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

M ATTANASIO, NH UHLENHAUT, D SEELOW… - Nature …, 2007 - pascal-francis.inist.fr
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and
fibrosis CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.

M Attanasio, NH Uhlenhaut, VH Sousa… - Nature …, 2007 - search.ebscohost.com
Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent
genetic cause of end-stage renal failure in the first three decades of life. Positional cloning of …