proline and Abnormalities, Autosome

proline has been researched along with Abnormalities, Autosome in 20 studies

Research

Studies (20)

Timeframe	Studies, this research(%)	All Research%
pre-1990	13 (65.00)	18.7374
1990's	4 (20.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (10.00)	24.3611
2020's	1 (5.00)	2.80

Authors

Authors	Studies
Gupta, P; Kharwar, RN; Prajapati, P; Seth, CS	1
Singh, A; Singh, AK; Srivastava, AK	1
Akbaş, H; Akkus, Z; Atay, AE; Budak, T; Isi, H; Tekes, S; Yalcin, K	1
RUKAVISHNIKOV, IM	1
Creel, DJ; Richards, SC	1
Abrahamson, M; Andréasson, S; Ehinger, B; Fex, G; Polland, W; Ponjavic, V	1
Justice, P; Kanwar, YS; Krakower, CA; Manaligod, JR; Wong, PW	1
Chang, LT; Tuveson, RW	1
Berson, EL; Dryja, TP; Rosner, B; Sandberg, MA; Weigel-DiFranco, C	1
Fujie, K; Maeda, S; Nishi, J; Sugiyama, T; Wada, M	1
Fujita, S; Itakura, Y; Nakao, T; Oyanagi, K; Shiono, H; Tamura, Y; Tsuchiyama, A	1
Douglas, EP	1
Komrower, GM	1
Mullenbach, E; Rae, ME; Stodolsky, M	1
Hartman, PE; Roth, JR	1
Maniscalco, RM; Powell, GF; Rasco, MA	1
Anderson, CW	1
Kao, FT; Puck, TT	1
Durant, JL; Elsas, LJ; Rosenberg, LE	1
Beatty, AV; Beatty, JW	1

Reviews

1 review(s) available for proline and Abnormalities, Autosome

Article	Year
Mechanisms of suppression. Advances in genetics, 1973, Volume: 17 Topics: Arginine; Bacteriophages; Chromosome Aberrations; Escherichia coli; Fungi; Mutation; Peptide Chain Initiation, Translational; Peptide Chain Termination, Translational; Proline; Proteins; Recombination, Genetic; RNA, Transfer; Salmonella; Suppression, Genetic; Terminology as Topic	1973

Other Studies

19 other study(ies) available for proline and Abnormalities, Autosome

Article	Year
Nitric oxide mediated regulation of ascorbate-glutathione pathway alleviates mitotic aberrations and DNA damage in International journal of phytoremediation, 2023, Volume: 25, Issue:4 Topics: Antioxidants; Ascorbic Acid; Biodegradation, Environmental; Chromosome Aberrations; DNA Damage; Glutathione; Nitric Oxide; Onions; Oxidative Stress; Proline; Salt Stress; Seedlings; Sodium Chloride	2023
Exogenous application of salicylic acid to alleviate the toxic effects of insecticides in Vicia faba L. Environmental toxicology, 2013, Volume: 28, Issue:12 Topics: Carotenoids; Chromosome Aberrations; Chromosomes, Plant; Endosulfan; Insecticides; Mitosis; Plant Leaves; Plant Roots; Proline; Pyrethrins; Salicylic Acid; Seeds; Vicia faba	2013
Role of p53 codon 72 polymorphism in chromosomal aberrations and mitotic index in patients with chronic hepatitis B. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2012, Volume: 45, Issue:11 Topics: Adult; Arginine; Case-Control Studies; Chromosome Aberrations; Codon; Female; Genetic Predisposition to Disease; Genotype; Hepatitis B, Chronic; Humans; Male; Mitotic Index; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53	2012
[ON THE RADIATION-PROTECTIVE EFFECT OF ALANINE AND PROLINE ON HEREDITARY STRUCTURES OF MAMMALIAN BONE MARROW CELLS]. Radiobiologiia, 1963, Volume: 3 Topics: Alanine; Animals; Bone Marrow; Bone Marrow Cells; Cell Nucleus; Chromosome Aberrations; Chromosome Disorders; Mice; Proline; Radiation-Protective Agents; Research	1963
Pattern dystrophy and retinitis pigmentosa caused by a peripherin/RDS mutation. Retina (Philadelphia, Pa.), 1995, Volume: 15, Issue:1 Topics: Adult; Aged; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 6; Eye Proteins; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Mutation; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Proline; Retina; Retinal Degeneration; Retinitis Pigmentosa; Serine	1995
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu. Ophthalmic genetics, 1997, Volume: 18, Issue:2 Topics: Adult; Chromosome Aberrations; Chromosome Disorders; Electroretinography; Exons; Eye Diseases, Hereditary; Family Health; Female; Genes, Dominant; Genetic Testing; Heterozygote; Humans; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Proline; Retinitis Pigmentosa; Rhodopsin; Sequence Analysis, DNA; Sweden; Visual Acuity	1997
Biochemical, morphological and hybrid studies in hyperprolinemic mice. Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1975, Volume: 22, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Animals; Chromosome Aberrations; Chromosome Disorders; Genes, Recessive; Glycine; Humans; Hybridization, Genetic; Hydrogen-Ion Concentration; Hydroxyproline; Kidney; Liver; Mice; Mice, Inbred Strains; Mitochondria, Liver; Pedigree; Proline	1975
An unstable strain of Aspergillus foetidus segregating proline auxotrophs. Applied microbiology, 1975, Volume: 30, Issue:1 Topics: Aspergillus; Cell Nucleus; Centrifugation, Density Gradient; Chromosome Aberrations; Culture Media; Genetic Variation; Glucosidases; Hot Temperature; Inclusion Bodies, Viral; Methylnitronitrosoguanidine; Microscopy, Electron; Mutagens; Mutation; Proline; Spores, Fungal; Ultraviolet Rays	1975
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine. American journal of ophthalmology, 1991, May-15, Volume: 111, Issue:5 Topics: Adolescent; Adult; Amino Acid Sequence; Chromosome Aberrations; Chromosome Disorders; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Humans; Leucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Night Blindness; Pedigree; Proline; Retinitis Pigmentosa; Rhodopsin; Visual Fields	1991
Acute cytogenetic effects of tyramine, MTCAs, NaCl and soy sauce on rat bone marrow cells in vivo. Mutation research, 1990, Volume: 240, Issue:4 Topics: Animals; Bone Marrow; Carbolines; Chromosome Aberrations; Female; Glycine max; Mutagens; Proline; Rats; Sodium Chloride; Sodium Nitrite; Tyramine	1990
Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality. The Tohoku journal of experimental medicine, 1987, Volume: 151, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosomes, Human, Pair 10; Female; Humans; Infant, Newborn; Karyotyping; Liver; Proline; Proline Oxidase	1987
Hyperprolinaemia and gyrate atrophy of the choroid and retina in members of the same family. The British journal of ophthalmology, 1985, Volume: 69, Issue:8 Topics: Adult; Atrophy; Child; Choroid; Chromosome Aberrations; Chromosome Disorders; Female; Fundus Oculi; Humans; Hydroxyproline; Male; Myopia; Ornithine; Oxidoreductases Acting on CH-NH Group Donors; Proline; Proline Oxidase; Retina; Visual Acuity	1985
The philosophy and practice of screening for inherited diseases. Pediatrics, 1974, Volume: 53, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Child; Child, Preschool; Chromatography, Paper; Chromosome Aberrations; Clinical Enzyme Tests; Costs and Cost Analysis; Down Syndrome; Female; Genetic Counseling; Genetic Diseases, Inborn; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Karyotyping; Male; Mass Screening; Phenylketonurias; Philosophy, Medical; Pregnancy; Prenatal Diagnosis; Proline; Sex Determination Analysis	1974
The addition of lac+ chromosome fragments to the E. coli proA-proB-lac deletion 13 chromosome. Genetics, 1972, Volume: 70, Issue:4 Topics: Chromosome Aberrations; Chromosomes, Bacterial; Coliphages; Conjugation, Genetic; Crossing Over, Genetic; Escherichia coli; Genetic Linkage; Heterozygote; Lactose; Lysogeny; Models, Biological; Proline; Radiation Effects; Recombination, Genetic; Transduction, Genetic; Ultraviolet Rays	1972
A prolidase deficiency in man with iminopeptiduria. Metabolism: clinical and experimental, 1974, Volume: 23, Issue:6 Topics: Biological Assay; Child; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Dansyl Compounds; Diagnosis, Differential; Dipeptidases; Erythrocytes; Humans; Lathyrism; Leukocytes; Male; Metabolism, Inborn Errors; Peptides; Proline; Proteinuria; Renal Aminoacidurias; Syndrome; Time Factors	1974
Spontaneous deletion formation in several classes of Escherichia coli mutants deficient in recombination ability. Mutation research, 1970, Volume: 9, Issue:2 Topics: Alleles; Chromosome Aberrations; Chromosome Mapping; Colicins; Coliphages; Drug Resistance, Microbial; Escherichia coli; Mutation; Proline; Radiation Effects; Recombination, Genetic; Transduction, Genetic; Ultraviolet Rays	1970
Genetics of somatic mammalian cells. V. Treatment with 5-bromodeoxyuridine and visible light for isolation of nutritionally deficient mutants. Proceedings of the National Academy of Sciences of the United States of America, 1967, Volume: 58, Issue:3 Topics: Animals; Bromodeoxyuridine; Cell Division; Chromosome Aberrations; Cricetinae; Culture Techniques; DNA; Female; Light; Lung; Mutation; Ovary; Proline	1967
Familial iminoglycinuria. An inborn error of renal tubular transport. The New England journal of medicine, 1968, Jun-27, Volume: 278, Issue:26 Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Heterozygote; Homozygote; Humans; Hydroxyproline; Intellectual Disability; Intestinal Absorption; Kidney Function Tests; Male; Proline; Renal Tubular Transport, Inborn Errors	1968
Reduction of radiation damage to Tradescantia chromosomes by adenosine triphosphate, proline, and histidine. Genetics, 1966, Volume: 53, Issue:1 Topics: Adenosine Triphosphate; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Histidine; In Vitro Techniques; Plant Cells; Proline; Radiation Genetics	1966