Lattice_grid_med
Powered by LatticeGrid

Search Enter term and hit return. Use '*' for as a wildcard.

Publication Listing for the MeSH term abnormalities. Found 21 abstracts

no pagination
Evers K. Are You Dense? [Editorial]. Academic radiology. 2015 Apr 11;22(6):677-8.
Kocher NJ, Tomaszewski JJ, Parsons RB, Cronson BR, Altman H, Kutikov A. Splenogonadal fusion: a rare etiology of solid testicular mass. Urology. 2014 Jan;83(1):e1-2.   PMCID: Editorial
Milone L, Okhunov Z, Gumbs AA. Laparoscopic diagnosis of annular pancreas in a patient with mucinous cystoadenoma of the body of the pancreas. J Gastrointest Cancer. 2012 Jun;43(2):367-9.   PMCID: not NIH funded
Roberts JL, Buckley RH, Luo B, Pei JM, Lapidus A, Peri S, Wei Q, Shin J, Parrott RE, Dunbrack RL, Testa JR, Zhong XP, Wiest DL. CD45-deficient severe combined immunodeficiency caused by uniparental disomy. Proceedings of the National Academy of Sciences of the United States of America. 2012 Jun;109(26):10456-61.   PMCID: PMC3387083
Cortellino S, Wang C, Wang B, Bassi MR, Caretti E, Champeval D, Calmont A, Jarnik M, Burch J, Zaret KS, Larue L, Bellacosa A. Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4. Dev Biol. 2009 Jan;325(1):225-37.   PMCID: PMC2645042
Rhodes J, Amsterdam A, Sanda T, Moreau LA, McKenna K, Heinrichs S, Ganem NJ, Ho KW, Neuberg DS, Johnston A, Ahn Y, Kutok JL, Hromas R, Wray J, Lee C, Murphy C, Radtke I, Downing JR, Fleming MD, MacConaill LE, Amatruda JF, Gutierrez A, Galinsky I, Stone RM, Ross EA, Pellman DS, Kanki JP, Look AT. Emi1 maintains genomic integrity during zebrafish embryogenesis and cooperates with p53 in tumor suppression. Mol Cell Biol. 2009 Nov;29(21):5911-22.   PMCID: PMC2772726
Pulfer SK, Ciccotto SL, Gallo JM. Distribution of small magnetic particles in brain tumor-bearing rats. Journal of Neuro-Oncology. 1999 Jan;41(2):99-105.
Tricoli JV. Y chromosome enumeration in touch preparations from 42 prostate tumors by interphase fluorescence in situ hybridization analysis. Cancer Genetics and Cytogenetics. 1999 May;111(1):1-6.
Bell DW, Jhanwar SC, Testa JR. Multiple regions of allelic loss from chromosome arm 6q in malignant mesothelioma. Cancer Research. 1997 Sep 15;57(18):4057-62.
Fein DA, Hanlon AL, Corn BW, Curran WJ, Coia LR. The influence of lymphangiography on the development of hypothyroidism in patients irradiated for Hodgkin's disease. International Journal of Radiation Oncology Biology Physics. 1996 Aug;36(1):13-8.
Taguchi T, Zhou JY, Feder M, Litwin S, KleinSzanto AJ, Testa JR. Detection of aneuploidy in interphase nuclei from non-small cell lung carcinomas by fluorescence in situ hybridization using chromosome-specific repetitive DNA probes. Cancer Genetics and Cytogenetics. 1996 Jul 15;89(2):120-5.
Knudson A. Asbestos and Mesothelioma - Genetic Lessons from a Tragedy. Proceedings of the National Academy of Sciences of the United States of America. 1995 Nov 21;92(24):10819-20.
Cheng JQ, Jhanwar SC, Klein WM, Bell DW, Lee WC, Altomare DA, Nobori T, Olopade OI, Buckler AJ, Testa JR. P16 Alterations and Deletion Mapping of 9p21-P22 in Malignant Mesothelioma. Cancer Research. 1994 Nov;54(21):5547-51.
Magliocco AM, Brilliant MH. Genome Scanning Detects Genetic Alterations in Human Ovarian- Carcinoma. Human Mutation. 1994 Jan;4(2):141-9.
Testa JR, Siegfried JM, Liu ZM, Hunt JD, Feder MM, Litwin S, Zhou JY, Taguchi T, Keller SM. Cytogenetic Analysis of 63 Nonsmall Cell Lung Carcinomas - Recurrent Chromosome Alterations Amid Frequent and Widespread Genomic Upheaval. Genes Chromosomes & Cancer. 1994 Nov;11(3):178-94.
Knudson AG. Introduction to the Genetics of Primary Renal Tumors in Children. Medical and Pediatric Oncology. 1993 Jan;21(3):193-8.
Taguchi T, Jhanwar SC, Siegfried JM, Keller SM, Testa JR. Recurrent Deletions of Specific Chromosomal Sites in 1p, 3p, 6q, and 9p in Human-Malignant Mesothelioma. Cancer Research. 1993 Sep 15;53(18):4349-55.
Brilliant MH. The Mouse Pink-Eyed Dilution Locus - a Model for Aspects of Prader-Willi Syndrome, Angelman Syndrome, and a Form of Hypomelanosis of Ito. Mammalian Genome. 1992 Jan;3(4):187-91.
Miura I, Graziano SL, Cheng JQ, Doyle LA, Testa JR. Chromosome Alterations in Human Small-Cell Lung-Cancer - Frequent Involvement of 5q. Cancer Research. 1992 Mar;52(5):1322-8.
Nakatsu Y, Gondo Y, Brilliant MH. The P-Locus Is Closely Linked to the Mouse Homolog of a Gene from the Prader-Willi Chromosomal Region. Mammalian Genome. 1992 Jan;2(1):69-71.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term abnormalities

abnormalities cancer gene cytogenetic analysis deletion adenocarcinoma genetics deletions lines tumors hypopigmentation Embryonic Development Phenotype diagnosis amplification embryology involvement Female metabolism melanoma parental origin short arm p53 retinoblastoma carcinoma complications Messenger RNA trisomy-7 tissue distribution Homozygote particle size mutations Hedgehog Proteins Physicians' Practice Patterns oculocutaneous albinism Genome Tumor Suppressor Protein p53 Neoplasms Extremities neck irradiation Attitude of Health Personnel thyroid-dysfunction breast-cancer Male long arm chromosome-11 Hematopoiesis wilms-tumor dna- Radiology drash syndrome imprinting bladder-cancer tumorigenesis tumor-suppressor gene Apoptosis remission isodisomy insitu hybridization homozygous deletions brain Alleles 9p diagnostic imaging lung-cancer database ovarian cancer Spleen karyotypic characterization p-locus Testis Mutation heterozygosity hypothyroidism product Endodeoxyribonucleases angelman syndrome Adult model cell-cycle sequence Embryo Loss barrier transport adriamycin pleural mesothelioma radiation therapy surgery Intracellular Signaling Peptides and Proteins committee lymphography carcinogenesis Breast Neoplasms identification DNA Repair magnetic field pathology Multiple Abnormalities events targeted drug delivery Pancreatectomy carcinomas Developmental Gene Expression Regulation Pancreatic Neoplasms cell lung-cancer tyrosine phosphatase cd45 familial translocation rhabdoid tumor deficiency Myeloid Cells genetic-map copy number wilms tumor children staging laparotomy legislation & jurisprudence etiology Nonmammalian Embryo Gene Silencing ferrofluid congenital cytology wt1 lymphangiogram doxorubicin methods T cell receptor T lymphocyte-signaling Hodgkin's disease statistics & numerical data permeability region Cell Cycle Proteins Pancreas rtvl-h c-myc oncogene consequences computed-tomography adenosquamous carcinomas genome scanning Testicular Diseases 15q expression proximal 6q Splenectomy interferon genes Mammography radiotherapy disease Body Patterning protein
Last updated on Tuesday, August 04, 2020