proline and Muscular Atrophy

proline has been researched along with Muscular Atrophy in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Brown, AEX; Camplese, L; Fets, L; Hirabayashi, S; Kramer, HB; Mokochinski, JB; Newton, H; Wang, YF	1
Drac, H; Hausmanowa-Petrusewicz, I; Kabzińska, D; Kochański, A; Lupski, JR; Rowińska-Marcińska, K; Saifi, GM	1
Kissane, JM	1

Reviews

1 review(s) available for proline and Muscular Atrophy

Article	Year
Hereditary disorders of the kidney. II. Hereditary nephropathies. Perspectives in pediatric pathology, 1973, Volume: 1 Topics: Adolescent; Adult; Aldosterone; Amyloidosis; Bone Resorption; Child; Child, Preschool; Female; Glomerulonephritis; Humans; Infant; Juxtaglomerular Apparatus; Kidney; Kidney Calculi; Kidney Diseases; Kidney Neoplasms; Laurence-Moon Syndrome; Lipodystrophy; Male; Metabolic Diseases; Middle Aged; Muscular Atrophy; Nail-Patella Syndrome; Nephritis; Nephrotic Syndrome; Potassium; Proline; Renal Tubular Transport, Inborn Errors	1973

Article

Year

Hereditary disorders of the kidney. II. Hereditary nephropathies.

Perspectives in pediatric pathology, 1973, Volume: 1

Topics: Adolescent; Adult; Aldosterone; Amyloidosis; Bone Resorption; Child; Child, Preschool; Female; Glomerulonephritis; Humans; Infant; Juxtaglomerular Apparatus; Kidney; Kidney Calculi; Kidney Diseases; Kidney Neoplasms; Laurence-Moon Syndrome; Lipodystrophy; Male; Metabolic Diseases; Middle Aged; Muscular Atrophy; Nail-Patella Syndrome; Nephritis; Nephrotic Syndrome; Potassium; Proline; Renal Tubular Transport, Inborn Errors

1973

Other Studies

2 other study(ies) available for proline and Muscular Atrophy

Article	Year
Systemic muscle wasting and coordinated tumour response drive tumourigenesis. Nature communications, 2020, 09-16, Volume: 11, Issue:1 Topics: Amino Acid Transport Systems; Animals; Animals, Genetically Modified; Carcinogenesis; Dietary Sugars; Drosophila melanogaster; Drosophila Proteins; Fibroblast Growth Factors; Gene Expression Profiling; Hemolymph; Larva; Muscle Weakness; Muscle, Skeletal; Muscular Atrophy; Neoplasms, Experimental; Nuclear Proteins; Proline; ras Proteins; Receptor Protein-Tyrosine Kinases; Trans-Activators; YAP-Signaling Proteins	2020
Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2007, Volume: 26, Issue:2 Topics: Adult; Amino Acid Sequence; Charcot-Marie-Tooth Disease; Genotype; GTP Phosphohydrolases; Humans; Leucine; Male; Membrane Proteins; Membrane Transport Proteins; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Molecular Sequence Data; Muscular Atrophy; Mutation; Nerve Tissue Proteins; Phenotype; Poland; Proline	2007

Article

Year

Systemic muscle wasting and coordinated tumour response drive tumourigenesis.

Nature communications, 2020, 09-16, Volume: 11, Issue:1

Topics: Amino Acid Transport Systems; Animals; Animals, Genetically Modified; Carcinogenesis; Dietary Sugars; Drosophila melanogaster; Drosophila Proteins; Fibroblast Growth Factors; Gene Expression Profiling; Hemolymph; Larva; Muscle Weakness; Muscle, Skeletal; Muscular Atrophy; Neoplasms, Experimental; Nuclear Proteins; Proline; ras Proteins; Receptor Protein-Tyrosine Kinases; Trans-Activators; YAP-Signaling Proteins

2020

Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2007, Volume: 26, Issue:2

Topics: Adult; Amino Acid Sequence; Charcot-Marie-Tooth Disease; Genotype; GTP Phosphohydrolases; Humans; Leucine; Male; Membrane Proteins; Membrane Transport Proteins; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Molecular Sequence Data; Muscular Atrophy; Mutation; Nerve Tissue Proteins; Phenotype; Poland; Proline

2007