Compounds > proline

proline and Chromosome Deletion

proline has been researched along with Chromosome Deletion in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (31.25)	18.7374
1990's	5 (31.25)	18.2507
2000's	4 (25.00)	29.6817
2010's	2 (12.50)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chen, HJ; Chen, ZZ; Wu, SQ; Xiong, DL; Xu, ZS; Zhan, R; Zhang, JS; Zhang, JY	1
Dornhoffer, J; Hartzell, LD; McKelvey, KD; Van Hemert, RL	1
Baggish, JS; Berger, M; Hagan, JB; Lohrmann, E; Shashi, V; Spycher, MO; Sullivan, KE; Wasserman, RL	1
Berthelot, J; Bonneau, D; Bonnemains, C; Campion, D; Frebourg, T; Jacquet, H; Raux, G; Saugier-Veber, P; Simard, G	1
Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J	1
Arst, HN; Bailey, CR; Jones, SA	1
Appel, LF; Cai, J; Lan, Y; Weir, M	1
Ferrell, RE; Gass, JD; Gorin, MB; Jackson, KE; Jacobson, SG; Mitchell, E; Sheffield, VC; Stone, EM	1
Abdollahi, A; Godwin, AK; Hamilton, TC; Roberts, D; Schultz, DC; Sonoda, G; Testa, JR	1
Goodman, BK; Lin, WW; Pulver, AE; Rutberg, J; Thomas, GH	1
Brennan, SO; George, PM; Higuchi, R; Myles, T; Symmans, WA; Williamson, D	1
Maloy, S; O'Brien, K; Ostrovsky de Spicer, P	1
Arst, HN; Green, PM; Hull, EP; Scazzocchio, C	1
Brandriss, MC; Siddiqui, AH	1
Dila, DK; Maloy, SR	1
Arst, HN; Sharma, KK	1

Reviews

1 review(s) available for proline and Chromosome Deletion

Article	Year
Safety of L-proline as a stabilizer for immunoglobulin products. Expert review of clinical immunology, 2012, Volume: 8, Issue:2 Topics: Animals; Chromosome Deletion; Chromosomes, Human, Pair 22; Drug Stability; Drug-Related Side Effects and Adverse Reactions; Excipients; Genetic Diseases, Inborn; Humans; Immunoglobulin G; Immunoglobulins, Intravenous; Proline	2012

Other Studies

15 other study(ies) available for proline and Chromosome Deletion

Article	Year
Constitutive activation of NF-κB signaling by NOTCH1 mutations in chronic lymphocytic leukemia. Oncology reports, 2015, Volume: 33, Issue:4 Topics: Aged; Apoptosis; B-Lymphocytes; Chromosome Deletion; Chromosomes, Human, Pair 12; Chromosomes, Human, Pair 13; DNA, Neoplasm; Female; Frameshift Mutation; Gene Expression Regulation, Leukemic; Humans; Leukemia, Lymphocytic, Chronic, B-Cell; Male; Middle Aged; Neoplasm Proteins; NF-kappa B; Oligopeptides; Proline; Protein Structure, Tertiary; Receptor, Notch1; RNA, Messenger; RNA, Neoplasm; Thiocarbamates; Transcription Factor RelA; Transcription Factor RelB; Trisomy	2015
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
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene. Journal of medical genetics, 2003, Volume: 40, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 22; Consanguinity; Homozygote; Humans; Male; Phenotype; Proline; Proline Oxidase	2003
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human molecular genetics, 2007, Jan-01, Volume: 16, Issue:1 Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors	2007
A method for the selection of deletion mutations in the L-proline catabolism gene cluster of Aspergillus nidulans. Genetical research, 1981, Volume: 38, Issue:2 Topics: Aspergillus nidulans; Chromosome Deletion; Genes; Genetic Techniques; Mutation; Proline	1981
Dissection of the Drosophila paired protein: functional requirements for conserved motifs. Mechanisms of development, 1994, Volume: 47, Issue:2 Topics: Amino Acid Sequence; Animals; Cell Line; Chromosome Deletion; DNA-Binding Proteins; Drosophila; Homeodomain Proteins; Molecular Sequence Data; Multigene Family; Mutation; Proline; Protein Structure, Tertiary; Repetitive Sequences, Nucleic Acid; Transcription, Genetic	1994
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Ophthalmology, 1995, Volume: 102, Issue:2 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Chromosome Deletion; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Macular Degeneration; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Phenotype; Point Mutation; Polymerase Chain Reaction; Proline; Retinal Degeneration; Visual Fields	1995
Identification of a zinc-finger gene at 6q25: a chromosomal region implicated in development of many solid tumors. Oncogene, 1997, Apr-24, Volume: 14, Issue:16 Topics: Amino Acid Sequence; Animals; Cell Cycle Proteins; Cell Line, Transformed; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 6; Cloning, Molecular; DNA-Binding Proteins; DNA, Complementary; Epithelium; Female; Genes, Tumor Suppressor; Glutamine; Humans; In Situ Hybridization, Fluorescence; Molecular Sequence Data; Ovarian Neoplasms; Ovary; Polymerase Chain Reaction; Proline; Rats; Sequence Homology, Amino Acid; Transcription Factors; Tumor Suppressor Proteins; Zinc Fingers	1997
Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome. Journal of inherited metabolic disease, 2000, Volume: 23, Issue:8 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Biomarkers; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 22; Female; Humans; Infant; Infant, Newborn; Male; Proline; Proline Oxidase; Syndrome	2000
A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide level. British journal of haematology, 1992, Volume: 81, Issue:1 Topics: Anemia, Hemolytic; Base Sequence; Blotting, Southern; Chromosome Deletion; Codon; DNA; Female; Globins; Hemoglobins, Abnormal; Humans; Leucine; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Proline; RNA, Messenger	1992
Regulation of proline utilization in Salmonella typhimurium: a membrane-associated dehydrogenase binds DNA in vitro. Journal of bacteriology, 1991, Volume: 173, Issue:1 Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Sequence; Base Sequence; Cell Membrane; Chromosome Deletion; DNA, Bacterial; Gene Amplification; Genes, Bacterial; Models, Molecular; Molecular Sequence Data; Nucleic Acid Conformation; Oxidoreductases Acting on CH-NH Group Donors; Plasmids; Proline; Proline Oxidase; Protein Binding; Restriction Mapping; Salmonella typhimurium; Software	1991
Cloning and physical characterization of the L-proline catabolism gene cluster of Aspergillus nidulans. Molecular microbiology, 1989, Volume: 3, Issue:4 Topics: Aspergillus nidulans; Blotting, Northern; Blotting, Southern; Chromosome Deletion; Cloning, Molecular; Genes; Genes, Fungal; Multigene Family; Mutation; Plasmids; Proline; Recombination, Genetic; Restriction Mapping; RNA, Fungal; RNA, Messenger; Transcription, Genetic; Translocation, Genetic	1989
A regulatory region responsible for proline-specific induction of the yeast PUT2 gene is adjacent to its TATA box. Molecular and cellular biology, 1988, Volume: 8, Issue:11 Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Base Sequence; Chromosome Deletion; DNA, Fungal; Gene Expression Regulation; Genes, Fungal; Molecular Sequence Data; Proline; Promoter Regions, Genetic; Repetitive Sequences, Nucleic Acid; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins	1988
Proline transport in Salmonella typhimurium: putP permease mutants with altered substrate specificity. Journal of bacteriology, 1986, Volume: 168, Issue:2 Topics: Amino Acid Transport Systems, Neutral; Azetidinecarboxylic Acid; Binding Sites; Biological Transport, Active; Chromosome Deletion; Chromosome Mapping; Genes, Bacterial; Kinetics; Membrane Transport Proteins; Mutation; Proline; Salmonella typhimurium; Substrate Specificity	1986
The product of the regulatory gene of the proline catabolism gene cluster of Aspergillus nidulans is a positive-acting protein. Current genetics, 1985, Volume: 9, Issue:4 Topics: Aspergillus nidulans; Chromosome Deletion; Fungal Proteins; Genes; Genes, Fungal; Genes, Regulator; Mutation; Proline	1985