Works matching Human chromosome abnormalities

Results: 100

Chromosome abnormalities in human epithelial ovarian malignancies.

Published in:

International Journal of Gynecology & Obstetrics, 1991, v. 36, n. 1, p. 79, doi. 10.1016/0020-7292(91)90191-7

By:

Gallion, HH;
Powell, DE;
Smith, LW;
Morrow, JK;
Martin, AW;
Van Nagell, JR;
Donaldson, ES

Publication type:

Article

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).

Published in:

Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 201, doi. 10.1002/gcc.1136

By:

Cohen, Ninette;
Betts, David R.;
Trakhtenbrot, Luba;
Niggli, Felix K.;
Amariglio, Ninette;
Brok-Simoni, Frida;
Rechavi, Gideon;
Meitar, Dafna

Publication type:

Article

Identification of multiple chromosome 12 abnormalities in human testicular germ cell tumors by two-color fluorescence in situ hybridization (FISH).

Published in:

Genes, Chromosomes & Cancer, 1995, v. 14, n. 4, p. 252, doi. 10.1002/gcc.2870140403

By:

Smolarek, Teresa A.;
Blough, Ruthann I.;
Foster, Richard S.;
Ulbright, Thomas M.;
Palmer, Catherine G.;
Heerema, Nyla A.

Publication type:

Article

Clonal chromosome abnormalities in human breast carcinomas I. Twenty-eight cases with primary disease.

Published in:

Genes, Chromosomes & Cancer, 1993, v. 7, n. 4, p. 185, doi. 10.1002/gcc.2870070402

By:

Thompson, Floyd;
Emerson, Julia;
Dalton, William;
Yang, Jin-Ming;
McGee, Daniel;
Villar, Hugo;
Knox, Sally;
Massey, Kathy;
Weinstein, Ronald;
Bhattacharyya, Achyut;
Trent, Jeffrey

Publication type:

Article

Clonal chromosome abnormalities in human breast carcinomas II. Thirty-four cases with metastatic disease.

Published in:

Genes, Chromosomes & Cancer, 1993, v. 7, n. 4, p. 194, doi. 10.1002/gcc.2870070403

By:

Trent, Jeffrey;
Yang, Jin-Ming;
Emerson, Julia;
Dalton, William;
McGee, Daniel;
Massey, Kathy;
Thompson, Floyd;
Villar, Hugo

Publication type:

Article

Abnormalities of chromosomes 7 and 22 in human malignant pleural mesothelioma: Correlation between southern blot and cytogenetic analyses.

Published in:

Genes, Chromosomes & Cancer, 1992, v. 4, n. 2, p. 176, doi. 10.1002/gcc.2870040212

By:

Tiainen, Marianne;
Kere, Juha;
Knuutila, Sakari;
Tammilehto, Lauri;
Mattson, Kann

Publication type:

Article

Cytogenetic and molecular analysis of human male germ cell tumors: Chromosome 12 abnormalities and gene amplification.

Published in:

Genes, Chromosomes & Cancer, 1990, v. 1, n. 4, p. 289, doi. 10.1002/gcc.2870010406

By:

Samaniego, Felipe;
Rodriguez, Eduardo;
Houldsworth, Jane;
Murty, Vundavalli V. V. S.;
Ladanyi, Marc;
Lele, Kusum P.;
Chen, Quanguang;
Dmitrovsky, Ethan;
Geller, Nancy L.;
Reuter, Victor;
Jhanwar, Suresh C.;
Bosl, George J.;
Chaganti, R. S. K.

Publication type:

Article

Increased incidence of numerical chromosome abnormalities in spermatozoa injected into human oocytes by ICSI.

Published in:

2001

By:

Macas, Ervin;
Imthurn, Bruno;
Keller, Paul J.;
Macas, E;
Imthurn, B;
Keller, P J

Publication type:

journal article

Treatment-related chromosome abnormalities in human embryos.

Published in:

Human Reproduction, 1997, v. 12, n. 4, p. 780, doi. 10.1093/humrep/12.4.780

By:

Munne, S;
Magli, C;
Adler, A;
Wright, G;
de Boer, K;
Mortimer, D;
Tucker, M;
Cohen, J;
Gianaroli, L

Publication type:

Article

Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitation.

Published in:

1991

By:

Benet, J.;
Navarro, J.;
Genescà, A.;
Egozcue, J.;
Templado, C.

Publication type:

journal article

Chromosome abnormality rates in human embryos obtained from in-vitro maturation and IVF treatment cycles.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 4, p. 552, doi. 10.1016/j.rbmo.2010.05.002

By:

Xiao Yun Zhang;
Ata, Baris;
Weon-Young Son;
Buckett, William M.;
Seang-Lin Tan;
Asangla Ao

Publication type:

Article

A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S24, doi. 10.1016/S1472-6483(10)62320-6

By:

Iourov, I. Y.;
Vorsanova, S. G.;
Liehr, T.;
Soloviev, I. V.;
Yurov, Y. B.

Publication type:

Article

Advanced age increases chromosome structural abnormalities in human spermatozoa.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 2, p. 145, doi. 10.1038/ejhg.2010.166

By:

Templado, Cristina;
Donate, Anna;
Giraldo, Jesús;
Bosch, Mercè;
Estop, Anna

Publication type:

Article

Linear increase of structural and numerical chromosome 9 abnormalities in human sperm regarding age.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 10, p. 754, doi. 10.1038/sj.ejhg.5201049

By:

Bosch, Merce;
Rajmil, Osvaldo;
Egozcue, Josep;
Templado, Cristina

Publication type:

Article

Temporal changes in chromosome abnormalities in human spontaneous abortions: Results of 40 years of analysis.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 10, p. 2671, doi. 10.1002/ajmg.a.37795

By:

Hardy, Kathy;
Hardy, Philip J.;
Jacobs, Patricia A.;
Lewallen, Kevin;
Hassold, Terry J.

Publication type:

Article

Effect of culture conditions and media on the frequency of chromosomal abnormalities in human sperm chromosome complements.

Published in:

Molecular Reproduction & Development, 1990, v. 26, n. 2, p. 101, doi. 10.1002/mrd.1080260202

By:

Martin, Renee H.;
Templado, Cristina;
Ko, Evelyn;
Rademaker, Alfred

Publication type:

Article

Molecular analysis of chromosome 1,10 and 19 abnormalities in human oligodendroglial tumors: relationship between frequency of LOH grade, age and gender.

Published in:

Clinical Neuropathology, 2006, v. 25, n. 1, p. 18

By:

Gresner, S. M.;
Rieske, P.;
Wozniak, K.;
Piaskowski, S.;
Jaskolski, D. J.;
Skowronski, W.;
Golanska, E.;
Sikorska, B.;
Liberski, P. P.

Publication type:

Article

Chromosome abnormalities in human cancer. Report of a patient with chronic myelocytic leukemia and his nonleukemic monozygotic twin.

Published in:

Cancer (0008543X), 1966, v. 19, n. 6, p. 869, doi. 10.1002/1097-0142(196606)19:6<869::AID-CNCR2820190620>3.0.CO;2-O

By:

Jacobs, Edwin M.;
Luce, James K.;
Cailleau, Relda

Publication type:

Article

Paternal Age and Numerical Chromosome Abnormalities in Human Spermatozoa.

Published in:

Cytogenetic & Genome Research, 2016, v. 148, n. 4, p. 241, doi. 10.1159/000446724

By:

Donate, anna;
Estop, anna M.;
Giraldo, Jesús;
Templado, Cristina

Publication type:

Article

Chromosome Abnormalities in the Human Oocyte.

Published in:

Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 107, doi. 10.1159/000323801

By:

Fragouli, E.;
Wells, D.;
Delhanty, J. D. A.

Publication type:

Article

Frequency and distribution of chromosome abnormalities in human oocytes.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 193, doi. 10.1159/000086889

By:

Kuliev, A.;
Cieslak, J.;
Verlinsky, Y.

Publication type:

Article

Frequency and distribution of chromosome abnormalities in human spermatozoa.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 199, doi. 10.1159/000086890

By:

Templado, C.;
Bosch, M.;
Benet, J.

Publication type:

Article

Abnormalities of chromosome no. 1 in human solid malignant tumours.

Published in:

International Journal of Cancer, 1978, v. 21, n. 6, p. 688, doi. 10.1002/ijc.2910210604

By:

Kovacs, G. Y.

Publication type:

Article

Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific dna probes.

Published in:

Journal of Pathology, 1994, v. 172, n. 4, p. 325, doi. 10.1002/path.1711720407

By:

Zitzelsberger, Horst;
Szücs, Sandor;
Weier, Heinz-Ulrich;
Lehmann, Lars;
Braselmann, Herbert;
Enders, Susanne;
Schilling, Albrecht;
Breul, Jürgen;
Höfler, Heinz;
Bauchinger, Manfred

Publication type:

Article

Meiotic abnormalities in metaphase I human spermatocytes from infertile males: frequencies, chromosomes involved, and relationship with polymorphic karyotype and seminal parameters.

Published in:

Asian Journal of Andrology, 2014, v. 16, n. 6, p. 838, doi. 10.4103/1008-682X.135126

By:

Sarrate, Zaida;
Vidal, Francesca;
Blanco, Joan

Publication type:

Article

Human Chromosome Abnormalities as Related to Physical and Mental Dysfunction.

Published in:

Journal of Heredity, 1969, v. 60, n. 5, p. 239

By:

HELLER, JOHN H.

Publication type:

Article

Human Chromosome Abnormalities to be Subject of 1969 Key Lecture.

Published in:: Journal of Heredity, 1969, v. 60, n. 2, p. 70
Publication type:: Article

A Possible Specific Chromosome Abnormality in Human Chronic Myeloid Leukæmia.

Published in:

Nature, 1960, v. 188, n. 4757, p. 1165, doi. 10.1038/1881165a0

By:

BAIKIE, A. G.;
COURT-BROWN, W. M.;
BUCKTON, KARIN E.;
HARNDEN, D. G.;
JACOBS, PATRICIA A.;
TOUGH, ISHBEL M.

Publication type:

Article

Chromosome abnormalities in human embryos.

Published in:

1998

By:

Munné, S;
Cohen, J

Publication type:

journal article

Abnormalities of human sex chromosomes. V. A unifying concept in relation to the gonadal dysgeneses.

Published in:

Clinical Genetics, 1970, v. 1, n. 1, p. 15, doi. 10.1111/j.1399-0004.1970.tb01964.x

By:

German, James

Publication type:

Article

Detection of Numerical Chromosome Abnormalities in Human Spermatozoa by Three-Color Fluorescence in situ Hybridization.

Published in:

Journal of Obstetrics & Gynaecology Research, 1998, v. 24, n. 6, p. 385, doi. 10.1111/j.1447-0756.1998.tb00113.x

By:

Li, Ping;
Hoshiai, Hiroshi

Publication type:

Article

Chromosomal abnormalities in human glioblastomas: Gain in chromosome 7p correlating with loss in chromosome 10q.

Published in:

Molecular Carcinogenesis, 2003, v. 36, n. 1, p. 6, doi. 10.1002/mc.10085

By:

del Mar Inda, María;
Fan, Xing;
Muñoz, Jorge;
Perot, Christine;
Fauvet, Didier;
Danglot, Giselle;
Palacio, Ana;
Madero, Pilar;
Zazpe, Idoya;
Portillo, Eduardo;
Tuñón, Teresa;
Martínez-Peñuela, José María;
Alfaro, Jorge;
Eiras, José;
Bernheim, Alain;
Castresana, Javier S.

Publication type:

Article

Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

Published in:

Molecular Human Reproduction, 2008, v. 14, n. 2, p. 117

By:

Daphnis, D.D.;
Fragouli, E.;
Economou, K.;
Jerkovic, S.;
Craft, I.L.;
Delhanty, J.D.A.;
Harper, J.C.

Publication type:

Article

In vitro study of lymphocyte antiproliferation and cytogenetic effect by occupational formaldehyde exposure.

Published in:

Toxicology & Industrial Health, 2011, v. 27, n. 8, p. 719, doi. 10.1177/0748233710395991

By:

Pongsavee, M.

Publication type:

Article

Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals.

Published in:

PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005462

By:

Cloutier, Jeffrey M.;
Mahadevaiah, Shantha K.;
ElInati, Elias;
Nussenzweig, André;
Tóth, Attila;
Turner, James M. A.

Publication type:

Article

Euploidy rates in donor egg cycles significantly differ between fertility centers.

Published in:

2017

By:

Munné, S.;
Alikani, M.;
Ribustello, L.;
Colls, P.;
Martínez-Ortiz, Pedro A.;
McCulloh, D. H.;
Referring Physician Group

Publication type:

journal article

Use of microgenomic technology for analysis of alterations in DNA copy number and gene expression in malignant melanoma.

Published in:

Clinical & Experimental Immunology, 1997, v. 107, p. 33

By:

Trent, J. M.;
Bittner, M.;
Zhang, J.;
Wiltshire, R.;
Ray, M.;
Su, Y.;
Gracia, E.;
Meltzer, P.;
de Risi, J.;
Penland, L.;
Brown, P.

Publication type:

Article

CYTOGENETIC FINDINGS IN SERBIAN PATIENTS WITH KLINEFELTER SYNDROME.

Published in:

Genetika (0534-0012), 2020, v. 52, n. 1, p. 97, doi. 10.2298/GENSR2001097D

By:

ĐORĐEVIĆ, Vesna;
JEMUOVIĆ, Zvezdana;
PEKIĆ, Sandra;
DJUROVIĆ, Marina

Publication type:

Article

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

Published in:

Cytogenetics & Cell Genetics, 2001, v. 95, n. 3/4, p. 228, doi. 10.1159/000059350

By:

Lear, T. L.;
Houck, M. L.;
Zhang, Y. W.;
Debnar, L. A.;
Sutherland-Smith, M. R.;
Young, L.;
Jones, K. L.;
Benirschke, K.

Publication type:

Article

Aneuploidy in human sperm: a review of the frequency and distribution of aneuploidy, effects of donor age and lifestyle factors.

Published in:

Cytogenetics & Cell Genetics, 2000, v. 90, n. 3/4, p. 219, doi. 10.1159/000056773

By:

Shi, Q.;
Martin, R.H.

Publication type:

Article

The Relationship between Screening Markers in the First Trimester of Pregnancy and Chromosome Aberrations.

Published in:

International Journal of Preventive Medicine, 2022, v. 13, n. 1, p. 1, doi. 10.4103/ijpvm.IJPVM_572_20

By:

Mirsafaie, Maryam;
Moghaddam-Banaem, Lida;
Kheirollahi, Majid

Publication type:

Article

The First Report of a Patient with Trisomy 4p and Monosomy 10q.

Published in:

Archives of Iranian Medicine (AIM), 2019, v. 22, n. 7, p. 414

By:

Sobhani, Maryam;
Tahmasbi, Parisa;
Nasiri, Fatemeh;
Rahnama, Mitra;
Karimi-Nejad, Roxana;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Koller and the dawn of cancer cytogenetics.

Published in:

British Journal of Cancer, 2023, v. 128, n. 3, p. 402, doi. 10.1038/s41416-022-01996-z

By:

Norbury, Chris J.

Publication type:

Article

Quinacrine Fluorescence Patterns of Human D Group Chromosomes.

Published in:

Nature, 1971, v. 232, n. 5305, p. 24, doi. 10.1038/232024a0

By:

MILLER, D. A.;
ALLDERDICE, P. W.;
MILLER, O. J.;
BREG, W. R.

Publication type:

Article

The MAP-kinase ERK2 is a specific substrate of the protein tyrosine phosphatase HePTP.

Published in:

Oncogene, 2000, v. 19, n. 7, p. 858, doi. 10.1038/sj.onc.1203408

By:

Pettiford, Sherrie M;
Herbst, Ronald

Publication type:

Article

RELATIONSHIP BETWEEN GENETIC ANOMALIES OF DIFFERENT LEVELS AND DEVIATION IN DERMATOGLYPHIC TRAITS PART 3b: DERMATOGLYPHIC PECULIARITIES OF MALES WITH THE KLINEFELTER'S SYNDROME. MULTIVARIATE ANALYSIS.

Published in:

Papers on Anthropology, 2004, v. 13, p. 93

By:

Kobyliansky, Eugene;
Bejerano, Michal;
Yakovenko, Konstantin;
Katznelson, Mariassa Bat-Miriam

Publication type:

Article

Human nucleus pulposus cells significantly enhanced biological properties in a coculture system with direct cell-to-cell contact with autologous mesenchymal stem cells.

Published in:

Journal of Orthopaedic Research, 2010, v. 28, n. 5, p. 623, doi. 10.1002/jor.21036

By:

Watanabe, Takuya;
Sakai, Daisuke;
Yamamoto, Yukihiro;
Iwashina, Toru;
Serigano, Kenji;
Tamura, Futoshi;
Mochida, Joji

Publication type:

Article

Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures.

Published in:

BMC Genomics, 2003, v. 4, p. 1

By:

Sutcliffe, James S.;
Han, Michael K.;
Amin, Taneem;
Kesterson, Robert A.;
Nurmi, Erika L.

Publication type:

Article

Deoxyribonucleic Acid Replication of Somatic Cells in the Chinese Hamster.

Published in:

Nature, 1966, v. 210, n. 5040, p. 1074, doi. 10.1038/2101074a0

By:

PFLUEGER, OTTO H.;
YUNIS, JORGE J.

Publication type:

Article

Detection of structural and numerical chromosomal abnormalities by ACM‐FISH analysis in sperm of oligozoospermic infertility patients.

Published in:

Human Reproduction, 2004, v. 19, n. 6, p. 1395, doi. 10.1093/humrep/deh278

By:

T.E. Schmid;
M.H. Brinkworth;
F. Hill;
E. Sloter;
A. Kamischke;
F. Marchetti;
E. Nieschlag;
A.J. Wyrobek

Publication type:

Article