Compounds > proline

proline and Multiple Primary Neoplasms

proline has been researched along with Multiple Primary Neoplasms in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Alam, MS; Calhoun, B; Haldar, K; Liu, F; Lu, X; Sun, M; Wang, X; Zhang, C1
Dornhoffer, J; Hartzell, LD; McKelvey, KD; Van Hemert, RL1
Bouzourene, H; Gugerli, O; Halkic, N; Hutter, P; Monnerat, C; Vernez, M1
Blennow, E; Brauch, H; Brookwell, R; Giraud, S; Hii, SI; Larsson, C; Nicol, D; Nordenskjöld, M; Sahlén, S; Teh, BT1

Other Studies

4 other study(ies) available for proline and Multiple Primary Neoplasms

ArticleYear
Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing.
    BMC medical genetics, 2020, 02-27, Volume: 21, Issue:1

    Topics: Adrenal Gland Neoplasms; Cerebellar Neoplasms; Child; Child, Preschool; Family; Female; Frameshift Mutation; Germ-Line Mutation; Hemangioblastoma; Humans; Male; Middle Aged; Neoplasms, Multiple Primary; Pedigree; Pheochromocytoma; Proline; Retinal Neoplasms; RNA Splicing; Silent Mutation; Spinal Neoplasms; von Hippel-Lindau Disease; Von Hippel-Lindau Tumor Suppressor Protein

2020
Cerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation.
    The international tinnitus journal, 2008, Volume: 14, Issue:2

    Topics: Alleles; Amino Acid Substitution; Base Sequence; Cerebellar Neoplasms; Cerebellopontine Angle; Chromosome Deletion; Codon; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Neoplasms, Multiple Primary; Neuroma, Acoustic; Paraganglioma; Proline; Radiography; Radiosurgery; Succinate Dehydrogenase

2008
A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene.
    Familial cancer, 2007, Volume: 6, Issue:1

    Topics: Adenocarcinoma, Mucinous; Adenoma; Adult; Brain Neoplasms; Carcinoma; Cholangiocarcinoma; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Mutational Analysis; DNA Probes; DNA-Binding Proteins; Endometrial Neoplasms; Female; Germ-Line Mutation; Humans; Liver Neoplasms; Microsatellite Instability; Mutation, Missense; MutS Homolog 2 Protein; Neoplasms, Multiple Primary; Neoplastic Syndromes, Hereditary; Polyps; Proline; Sebaceous Gland Neoplasms; Serine; Skin Neoplasms; Syndrome

2007
Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution.
    Genes, chromosomes & cancer, 1998, Volume: 21, Issue:3

    Topics: Adenoma, Oxyphilic; Amino Acid Substitution; Arginine; Chromosomes, Human, Pair 8; Chromosomes, Human, Pair 9; Genes, Tumor Suppressor; Humans; Kidney Diseases, Cystic; Ligases; Male; Middle Aged; Neoplasms, Multiple Primary; Proline; Proteins; Translocation, Genetic; Tumor Suppressor Proteins; Ubiquitin-Protein Ligases; Von Hippel-Lindau Tumor Suppressor Protein

1998