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2-propanol and Abnormalities, Urogenital

2-propanol has been researched along with Abnormalities, Urogenital in 18 studies

2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.

Research Excerpts

ExcerptRelevanceReference
"The biologic peculiarities of tumors of early life are elucidated."2.35Neoplasia of early life and its relationships to teratogenesis. ( Bolande, RP, 1976)
"Gene dosage effects for catalase (CAT) were studied in two unrelated patients with an interstitial deletion involving 11p13 to determine precisely the sites of the genes for CAT and the Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad (WAGR) in the 11p13 band."1.27Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306. ( Hamawaki, M; Kasai, R; Kikkawa, K; Kimira, S; Kimoto, H; Matsuoka, K; Narahara, K; Ogata, M, 1984)
"An association of ocular colobomata and congenital heart disease was observed in seven patients."1.25Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs. ( Ho, CK; Kaufman, RL; Podos, SM, 1975)

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-199016 (88.89)18.7374
1990's2 (11.11)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Narahara, K1
Kikkawa, K1
Kimira, S1
Kimoto, H1
Ogata, M1
Kasai, R1
Hamawaki, M1
Matsuoka, K1
Niikawa, N1
Fukushima, Y1
Taniguchi, N1
Iizuka, S1
Kajii, T1
Li, FP1
Breslow, NE1
Morgan, JM1
Ghahremani, M1
Miller, GA1
Grundy, PE1
Green, DM1
Diller, LR1
Pelletier, J1
Huff, V1
Bolande, RP1
Ho, CK1
Kaufman, RL1
Podos, SM1
Couillin, P3
Azoulay, M2
Metezeau, P1
Grisard, MC1
Junien, C3
Gessler, M3
Thomas, GH1
McGillivray, BC1
Hayden, M1
Jaschek, G1
Bruns, GA3
Simola, KO2
Lavedan, C1
Barichard, F1
Molina Gomez, D1
Nicolas, H1
Quack, B1
Rethoré, MO1
Noel, B1
Seawright, A2
Fletcher, JM2
Fantes, JA1
Morrison, H1
Porteous, DJ2
Li, SS1
Hastie, ND1
Van Heyningen, V1
Bickmore, W1
Christie, S1
Boyd, PA1
Cranston, G1
Gosden, JR1
Rout, D1
DiGeorge, AM1
Harley, RD1
Knudson, AG1
Strong, LC1
De Andres Basauri, L1
Martínez, C1
Petersen, RA1
Boatman, DL1
Kölln, CP1
Flocks, RH1

Reviews

2 reviews available for 2-propanol and Abnormalities, Urogenital

ArticleYear
Neoplasia of early life and its relationships to teratogenesis.
    Perspectives in pediatric pathology, 1976, Volume: 3

    Topics: Abnormalities, Drug-Induced; Carcinoma, Basal Cell; Chromosome Aberrations; Chromosome Disorders; Co

1976
[Wilms' tumor and congenital malformations].
    Revista clinica espanola, 1973, Sep-15, Volume: 130, Issue:5

    Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Di

1973

Other Studies

16 other studies available for 2-propanol and Abnormalities, Urogenital

ArticleYear
Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.
    Human genetics, 1984, Volume: 66, Issue:2-3

    Topics: Abnormalities, Multiple; Adolescent; Catalase; Child, Preschool; Chromosome Banding; Chromosome Dele

1984
Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity.
    Human genetics, 1982, Volume: 60, Issue:4

    Topics: Catalase; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chrom

1982
Germline WT1 mutations in Wilms' tumor patients: preliminary results.
    Medical and pediatric oncology, 1996, Volume: 27, Issue:5

    Topics: Base Sequence; Exons; Genes, Wilms Tumor; Humans; Iris; Kidney Neoplasms; Mutation; Neoplasms, Multi

1996
Genotype/phenotype correlations in Wilms' tumor.
    Medical and pediatric oncology, 1996, Volume: 27, Issue:5

    Topics: Alleles; Amino Acid Sequence; Antisense Elements (Genetics); Child; Consensus Sequence; DNA Transpos

1996
Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs.
    Journal of medical genetics, 1975, Volume: 12, Issue:3

    Topics: Abnormalities, Multiple; Bone and Bones; Central Nervous System; Coloboma; Female; Heart Defects, Co

1975
The gene for catalase is assigned between the antigen loci MIC4 and MIC11.
    Genomics, 1989, Volume: 4, Issue:1

    Topics: Antigens; Catalase; Child; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Fem

1989
A deletion map of the WAGR region on chromosome 11.
    American journal of human genetics, 1989, Volume: 44, Issue:4

    Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA P

1989
Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.
    Science (New York, N.Y.), 1989, Jun-30, Volume: 244, Issue:4912

    Topics: Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 4; Cl

1989
Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.
    Cytogenetics and cell genetics, 1989, Volume: 50, Issue:2-3

    Topics: Adult; Blotting, Southern; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Ch

1989
Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
    Somatic cell and molecular genetics, 1988, Volume: 14, Issue:1

    Topics: Animals; Cell Separation; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; DNA;

1988
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
    Genomics, 1988, Volume: 3, Issue:2

    Topics: Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 11; Cloning, Molecular; DNA; Electrophoresi

1988
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
    Proceedings of the National Academy of Sciences of the United States of America, 1987, Volume: 84, Issue:15

    Topics: Animals; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; Cloning, Molecular; D

1987
The association of aniridia, Wilms' tumor, and genital abnormalities.
    Archives of ophthalmology (Chicago, Ill. : 1960), 1966, Volume: 75, Issue:6

    Topics: Child, Preschool; Female; Humans; Infant; Iris; Male; Urogenital Abnormalities; Wilms Tumor

1966
Mutation and cancer: a model for Wilms' tumor of the kidney.
    Journal of the National Cancer Institute, 1972, Volume: 48, Issue:2

    Topics: Child, Preschool; Chromosomes; Diseases in Twins; Eye Neoplasms; Factor Analysis, Statistical; Femal

1972
Schmid-Fraccaro syndrome ("cat's eye" syndrome).
    Archives of ophthalmology (Chicago, Ill. : 1960), 1973, Volume: 90, Issue:4

    Topics: Abnormalities, Multiple; Adolescent; Anus, Imperforate; Cataract; Child; Choroid; Coloboma; Craniofa

1973
Congenital anomalies associated with horseshoe kidney.
    The Journal of urology, 1972, Volume: 107, Issue:2

    Topics: Abnormalities, Multiple; Adolescent; Cardiovascular Abnormalities; Central Nervous System; Chromosom

1972