leucine and Progeria

leucine has been researched along with Progeria in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Al-Haggar, M; Barakat, T; Madej-Pilarczyk, A; Puzianowska-Kuznicka, M; Shams, A	1
Abdel-Hadi, D; Ahmad, N; Al-Haggar, M; Bujnicki, JM; Hamed, S; Kozlowski, L; Madej-Pilarczyk, A; Puzianowska-Kuznicka, M; Shams, A; Yahia, S	1

Other Studies

2 other study(ies) available for leucine and Progeria

Article	Year
Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu LMNA mutation and in their asymptomatic heterozygotic mothers. Journal of clinical pathology, 2013, Volume: 66, Issue:11 Topics: Acro-Osteolysis; Adult; Amino Acid Substitution; Arginine; Biopsy; Case-Control Studies; Child; Child, Preschool; Egypt; Female; Heterozygote; Homozygote; Humans; Lamin Type A; Leucine; Lipodystrophy; Male; Mandible; Microscopy, Electron, Transmission; Mothers; Mutation, Missense; Pedigree; Progeria; Skin	2013
A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome. European journal of human genetics : EJHG, 2012, Volume: 20, Issue:11 Topics: Abnormalities, Multiple; Arginine; Child; Child, Preschool; Egypt; Female; Founder Effect; Heterozygote; Humans; Lamin Type A; Leucine; Mandible; Mutation, Missense; Pedigree; Polymorphism, Restriction Fragment Length; Progeria; Protein Stability; Syndrome	2012

Article

Year

Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu LMNA mutation and in their asymptomatic heterozygotic mothers.

Journal of clinical pathology, 2013, Volume: 66, Issue:11

Topics: Acro-Osteolysis; Adult; Amino Acid Substitution; Arginine; Biopsy; Case-Control Studies; Child; Child, Preschool; Egypt; Female; Heterozygote; Homozygote; Humans; Lamin Type A; Leucine; Lipodystrophy; Male; Mandible; Microscopy, Electron, Transmission; Mothers; Mutation, Missense; Pedigree; Progeria; Skin

2013

A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome.

European journal of human genetics : EJHG, 2012, Volume: 20, Issue:11

Topics: Abnormalities, Multiple; Arginine; Child; Child, Preschool; Egypt; Female; Founder Effect; Heterozygote; Humans; Lamin Type A; Leucine; Mandible; Mutation, Missense; Pedigree; Polymorphism, Restriction Fragment Length; Progeria; Protein Stability; Syndrome

2012