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Journal articles on the topic 'Abnormalities, Human'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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1

Winter, Robin M. "Analysing human developmental abnormalities." BioEssays 18, no. 12 (1996): 965–71. http://dx.doi.org/10.1002/bies.950181206.

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2

Benirschke, Kurt. "Abnormalities of the Human Placenta." NeoReviews 6, no. 9 (2005): e414-e423. http://dx.doi.org/10.1542/neo.6-9-e414.

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3

Munne, S. "Chromosome abnormalities in human embryos." Human Reproduction Update 4, no. 6 (1998): 842–55. http://dx.doi.org/10.1093/humupd/4.6.842.

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4

McFadden, Deborah E., and J. M. Friedman. "Chromosome abnormalities in human beings." Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 396, no. 1-2 (1997): 129–40. http://dx.doi.org/10.1016/s0027-5107(97)00179-6.

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5

Ferguson-Smith, M. A. "Abnormalities of human sex determination." Journal of Inherited Metabolic Disease 15, no. 4 (1992): 518–25. http://dx.doi.org/10.1007/bf01799610.

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6

Tsokos, G. C. "Lymphocyte abnormalities in human lupus." Clinical Immunology and Immunopathology 63, no. 1 (1992): 7–9. http://dx.doi.org/10.1016/0090-1229(92)90083-z.

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7

Linker-Israeli, Mariana. "Cytokine abnormalities in human lupus." Clinical Immunology and Immunopathology 63, no. 1 (1992): 10–12. http://dx.doi.org/10.1016/0090-1229(92)90084-2.

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8

Chung, Sung Ik, Sang Heun Baik, and Hong Tage Kim. "Chromosomal Abnormalities in Human Hepatoma." Korean Journal of Physical Anthropology 8, no. 2 (1995): 185. http://dx.doi.org/10.11637/kjpa.1995.8.2.185.

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9

Dadoune, J. P. "Ultrastructural abnormalities of human spermatozoa*." Human Reproduction 3, no. 3 (1988): 311–18. http://dx.doi.org/10.1093/oxfordjournals.humrep.a136701.

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10

Björntorp, Per. "Neuroendocrine abnormalities in human obesity." Metabolism 44 (February 1995): 38–41. http://dx.doi.org/10.1016/0026-0495(95)90208-2.

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11

Stratton, M. R., J. Darling, P. L. Lantos, C. S. Cooper, and B. R. Reeves. "Cytogenetic abnormalities in human ependymomas." International Journal of Cancer 44, no. 4 (1989): 579–81. http://dx.doi.org/10.1002/ijc.2910440403.

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12

Tagliavini, J., S. A. Gandolfi, and G. Maraini. "Cytoskeleton abnormalities in human senile cataract." Current Eye Research 5, no. 12 (1986): 903–10. http://dx.doi.org/10.3109/02713688608995170.

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13

Byrne, Edward. "Mitochondrial DNA abnormalities in human disease." Medical Journal of Australia 154, no. 10 (1991): 646–47. http://dx.doi.org/10.5694/j.1326-5377.1991.tb121246.x.

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14

Villegas, Ana, Fernando A. Gonzalez, and Eduardo Anguita. "Gfi1b Association to Human Hematological Abnormalities." Blood 108, no. 11 (2006): 3748. http://dx.doi.org/10.1182/blood.v108.11.3748.3748.

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Abstract Lineage specific transcription factors play essential roles in regulation of hematopoietic development. Transcription factor abnormalities have been frequently described in acute leukemia, mostly through cytogenetic changes. Nevertheless, point mutations can be easily missed. Recently, mutations in the erythroid and megakaryocyte specific transcription factor GATA1 have been discovered in patients with dyserythropoietic anemia and acute megakaryoblastic leukemia (AML-M7) with Down syndrome. Besides GATA-1, located on the X-chromosome, point mutations have been described in biallelic g

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15

Cryns, V. L. "p53 abnormalities in human parathyroid carcinoma." Journal of Clinical Endocrinology & Metabolism 78, no. 6 (1994): 1320–24. http://dx.doi.org/10.1210/jc.78.6.1320.

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16

Martin, Renée H. "Meiotic chromosome abnormalities in human spermatogenesis." Reproductive Toxicology 22, no. 2 (2006): 142–47. http://dx.doi.org/10.1016/j.reprotox.2006.03.013.

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17

Quigley, Anita, Robert Kapsa, Edward Byrne, and George Hale. "Mitochondrial abnormalities in human dilated cardiomyopathy." Journal of Cardiac Failure 4, no. 3 (1998): 15. http://dx.doi.org/10.1016/s1071-9164(98)90055-0.

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18

Migeon, Claude J., and Amy B. Wisniewski. "Human sex differentiation and its abnormalities." Best Practice & Research Clinical Obstetrics & Gynaecology 17, no. 1 (2003): 1–18. http://dx.doi.org/10.1053/ybeog.2003.0354.

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19

Cryns, V. L., M. P. Rubio, A. D. Thor, D. N. Louis, and A. Arnold. "p53 abnormalities in human parathyroid carcinoma." Journal of Clinical Endocrinology & Metabolism 78, no. 6 (1994): 1320–24. http://dx.doi.org/10.1210/jcem.78.6.8200932.

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20

Fragouli, E., D. Wells, and J. D. A. Delhanty. "Chromosome Abnormalities in the Human Oocyte." Cytogenetic and Genome Research 133, no. 2-4 (2011): 107–18. http://dx.doi.org/10.1159/000323801.

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21

Hassold, Terry J. "Chromosome abnormalities in human reproductive wastage." Trends in Genetics 2 (January 1986): 105–10. http://dx.doi.org/10.1016/0168-9525(86)90194-0.

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22

Lo Presti, Rosalia, Eugenia Hopps, and Gregorio Caimi. "Hemorheological abnormalities in human arterial hypertension." Korea-Australia Rheology Journal 26, no. 2 (2014): 199–204. http://dx.doi.org/10.1007/s13367-014-0021-5.

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23

Otsuki, Junko. "Intracytoplasmic Morphological Abnormalities in Human Oocytes." Journal of Mammalian Ova Research 26, no. 1 (2009): 26–31. http://dx.doi.org/10.1274/jmor.26.26.

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24

Bigner, Sandra H., Joachim Mark, Henry S. Friedman, Jaclyn A. Biegel, and Darell D. Bigner. "Structural chromosomal abnormalities in human medulloblastoma." Cancer Genetics and Cytogenetics 30, no. 1 (1988): 91–101. http://dx.doi.org/10.1016/0165-4608(88)90096-9.

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25

Mars, Wendy M., and Grady F. Saunders. "Chromosomal abnormalities in human breast cancer." CANCER AND METASTASIS REVIEW 9, no. 1 (1990): 35–43. http://dx.doi.org/10.1007/bf00047587.

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26

CHATENOUD, LUCIENNE. "Immunoregulatory Abnormalities in Primary Human Glomerulonephritis." Clinics in Immunology and Allergy 6, no. 2 (1986): 395–409. http://dx.doi.org/10.1016/s0260-4639(22)00084-6.

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27

George, Varghese, Sethu Babu, Sahoo RS, and Jha RK. "Lipid profile abnormalities in human immunodeficiency virus infected patients- a hospital based study." Asian Pacific Journal of Health Sciences 2, no. 1 (2015): 76–81. http://dx.doi.org/10.21276/apjhs.2015.2.1.13.

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28

Little, Karley Y., Lian Zhang, Timothy Desmond, Kirk A. Frey, Gregory W. Dalack, and Bader J. Cassin. "Striatal Dopaminergic Abnormalities in Human Cocaine Users." American Journal of Psychiatry 156, no. 2 (1999): 238–45. http://dx.doi.org/10.1176/ajp.156.2.238.

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29

Handyside, AH. "Abnormalities of human preimplantation development in vitro." Reproduction, Fertility and Development 4, no. 5 (1992): 481. http://dx.doi.org/10.1071/rd9920481.

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30

Munne, S., C. Magli, A. Adler, et al. "Treatment-related chromosome abnormalities in human embryos." Human Reproduction 12, no. 4 (1997): 780–84. http://dx.doi.org/10.1093/humrep/12.4.780.

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31

Abdul-Latif, Hussein, Milton R. Brown, and John S. Parks. "Abnormalities of the Human Growth Hormone Gene." Endocrinologist 3, no. 6 (1993): 409–14. http://dx.doi.org/10.1097/00019616-199311000-00009.

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32

Steinberger, E., and E. Weidman. "Abnormalities of Spermatogenesis in the Human Testes." Seminars in Reproductive Medicine 6, no. 04 (1988): 309–21. http://dx.doi.org/10.1055/s-2007-1021367.

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33

CLERICI, MARIO, MASSIMO GALLI, SIMONA BOSIS, CRISTINA GERVASONI, MAURO MORONI, and GUIDO NORBIATO. "Immunoendocrinologic Abnormalities in Human Immunodeficiency Virus Infection." Annals of the New York Academy of Sciences 917, no. 1 (2006): 956–61. http://dx.doi.org/10.1111/j.1749-6632.2000.tb05462.x.

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34

Pope, F. M., and A. C. Nicholls. "Molecular abnormalities of collagen in human disease." Archives of Disease in Childhood 62, no. 5 (1987): 523–28. http://dx.doi.org/10.1136/adc.62.5.523.

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35

Lambert-Messerlian, G. M., H. Pinar, E. Laprade, U. Tantravahi, A. Schneyer, and J. A. Canick. "Inhibins and activins in human fetal abnormalities." Molecular and Cellular Endocrinology 225, no. 1-2 (2004): 101–8. http://dx.doi.org/10.1016/j.mce.2004.02.019.

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36

Krakoff, Irwin H., and M. Earl Balis. "ABNORMALITIES OF PURINE METABOLISM IN HUMAN LEUKEMIA*." Annals of the New York Academy of Sciences 113, no. 2 (2006): 1043–52. http://dx.doi.org/10.1111/j.1749-6632.1964.tb40722.x.

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37

Gallion, H. H., D. E. Powell, L. W. Smith, et al. "Chromosome abnormalities in human epithelial ovarian malignancies." Gynecologic Oncology 38, no. 3 (1990): 473–77. http://dx.doi.org/10.1016/0090-8258(90)90094-2.

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38

Gallion, HH, DE Powell, LW Smith, et al. "Chromosome abnormalities in human epithelial ovarian malignancies." International Journal of Gynecology & Obstetrics 36, no. 1 (1991): 79. http://dx.doi.org/10.1016/0020-7292(91)90191-7.

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39

Edvard Smith, C. I., and Lennart Hammarström. "Gene abnormalities in human immunoglobulin deficiency disorders." Clinical Immunology Newsletter 7, no. 10 (1986): 145–49. http://dx.doi.org/10.1016/0197-1859(86)90060-9.

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40

Yawata, Yoshihito. "Band 4.2 Abnormalities in Human Red Cells." American Journal of the Medical Sciences 307, no. 3 (1994): 190–203. http://dx.doi.org/10.1097/00000441-199403000-00006.

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41

WEISBERG, LEON A. "Neurologic Abnormalities in Human Immunodeficiency Virus Infection." Southern Medical Journal 94, no. 3 (2001): 266–75. http://dx.doi.org/10.1097/00007611-200103000-00001.

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42

WEISBERG, LEON A. "Neurologic Abnormalities in Human Immunodeficiency Virus Infection." Southern Medical Journal 94, no. 3 (2001): 266–75. http://dx.doi.org/10.1097/00007611-200194030-00001.

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43

Pastakia, K. B., N. E. Brownson, D. A. Terle, and B. J. Poindexter. "Amphotericin B induced abnormalities in human platelets." Molecular Pathology 49, no. 5 (1996): M301—M307. http://dx.doi.org/10.1136/mp.49.5.m301.

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44

Plachot, M., and N. Crozet. "Fertilization abnormalities in human in-vitro fertilization." Human Reproduction 7, suppl 1 (1992): 89–94. http://dx.doi.org/10.1093/humrep/7.suppl_1.89.

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45

Sandberg, Avery A. "Chromosome abnormalities in human cancer and leukemia." Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 247, no. 2 (1991): 231–40. http://dx.doi.org/10.1016/0027-5107(91)90019-k.

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46

Grammatico, P., M. L. Lo Re, S. Scarpa, A. Modesti, and G. Del Porto. "Human malignant melanoma significance of chromosomal abnormalities." Cancer Genetics and Cytogenetics 48, no. 2 (1990): 237–42. http://dx.doi.org/10.1016/0165-4608(90)90126-u.

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47

Sebag, J. "Abnormalities of human vitreous structure in diabetes." Graefe's Archive for Clinical and Experimental Ophthalmology 231, no. 5 (1993): 257–60. http://dx.doi.org/10.1007/bf00919101.

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48

Potluri, Venkateswara R., Lawrence Helson, Robert M. Ellsworth, Theodore Reid, and Fred Gilbert. "Chromosomal abnormalities in human retinoblastoma a review." Cancer 58, no. 3 (1986): 663–71. http://dx.doi.org/10.1002/1097-0142(19860801)58:3<663::aid-cncr2820580311>3.0.co;2-g.

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49

Uckun, FM, KJ Gajl-Peczalska, AJ Provisor, and NA Heerema. "Immunophenotype-karyotype associations in human acute lymphoblastic leukemia." Blood 73, no. 1 (1989): 271–80. http://dx.doi.org/10.1182/blood.v73.1.271.271.

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Abstract The present study is a detailed analysis of the cytogenetic features of leukemic cells from 104 immunologically classified acute lymphoblastic leukemia (ALL) (78 B lineage and 26 T lineage) cases. Clonal chromosomal abnormalities were found in marrow blasts from 77 of 104 (74%) cases. Hyperdiploidy was much more frequent in B-lineage ALL cases, whereas normal diploidy was more common in T-lineage ALL cases. Fifty-nine of 104 cases (46 of 78 B-lineage ALL and 13 of 26 T-lineage ALL cases) had structural chromosomal abnormalities. Structural abnormalities involving 2p11, 7p13, 7p22, pro

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50

Uckun, FM, KJ Gajl-Peczalska, AJ Provisor, and NA Heerema. "Immunophenotype-karyotype associations in human acute lymphoblastic leukemia." Blood 73, no. 1 (1989): 271–80. http://dx.doi.org/10.1182/blood.v73.1.271.bloodjournal731271.

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The present study is a detailed analysis of the cytogenetic features of leukemic cells from 104 immunologically classified acute lymphoblastic leukemia (ALL) (78 B lineage and 26 T lineage) cases. Clonal chromosomal abnormalities were found in marrow blasts from 77 of 104 (74%) cases. Hyperdiploidy was much more frequent in B-lineage ALL cases, whereas normal diploidy was more common in T-lineage ALL cases. Fifty-nine of 104 cases (46 of 78 B-lineage ALL and 13 of 26 T-lineage ALL cases) had structural chromosomal abnormalities. Structural abnormalities involving 2p11, 7p13, 7p22, proximal q a

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