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Search Results - Matsell, Eli
Search Results - Matsell, Eli
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Outcomes of solitary functioning kidneys—renal agenesis is different than multicystic dysplastic kidney disease
by
Matsell, Douglas G.
,
Bao, Carol
,
Po White, Teagan
,
Chan, Ella
,
Matsell, Eli
,
Cojocaru, Dan
,
Catapang, Marisa
Published in
Pediatric nephrology (Berlin, West)
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Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases
by
Matsell, Eli
,
Andersen, Jens Peter
,
Molday, Robert S
Published in
Disease models & mechanisms
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First person – Eli Matsell
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Disease models & mechanisms
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The impact of small kidneys
by
Matsell, Douglas G.
,
Cojocaru, Dan
,
Matsell, Eli W.
,
Eddy, Allison A.
Published in
Pediatric nephrology (Berlin, West)
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Kidney length standardized to body length predicts outcome in infants with a solitary functioning kidney
by
Matsell, Douglas G.
,
Bao, Carol
,
White, Teagan Po
,
Chan, Ella
,
Matsell, Eli
,
Cojocaru, Dan
,
Bajno, Lydia
,
Catapang, Marisa
Published in
Pediatric nephrology (Berlin, West)
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Structural and functional properties of the N and C terminal segments of the P4-ATPase phospholipid flippase ATP8A2
by
Matsell, Eli
,
Mazaheri, Moloud
,
Andersen, Jens Peter
,
Molday, Robert S
Published in
The Journal of biological chemistry
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On the track of the lipid transport pathway of the phospholipid flippase ATP8A2 - Mutation analysis of residues of the transmembrane segments M1, M2, M3 and M4
by
Mogensen, Louise S.
,
Mikkelsen, Stine A.
,
Tadini-Buoninsegni, Francesco
,
Holm, Rikke
,
Matsell, Eli
,
Vilsen, Bente
,
Molday, Robert S.
,
Andersen, Jens Peter
Published in
Biochimica et biophysica acta. Molecular cell research
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A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
by
Flannery, Kyle P.
,
Safwat, Sylvia
,
Matsell, Eli
,
Battula, Namarata
,
Hamed, Ahlam A. A.
,
Mohamed, Inaam N.
,
Elseed, Maha A.
,
Koko, Mahmoud
,
Abubaker, Rayan
,
Abozar, Fatima
,
Elsayed, Liena E. O.
,
Bhise, Vikram
,
Molday, Robert S.
,
Salih, Mustafa A.
,
Yahia, Ashraf
,
Manzini, M. Chiara
Published in
Neurogenetics
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