Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Abirami Chidambaram"'
Autor:
Bruce Budowle, Abirami Chidambaram, Jianye Ge, Ranajit Chakraborty, Orin Dym, Arthur J. Eisenberg, Meredith Turnbough, Michelle Collins, Jonathan L. King, Carey Davis
Publikováno v:
International Journal of Legal Medicine. 125:559-563
Y chromosome short tandem repeat (Y-STR) loci are important genetic markers for forensic biological evidence analyses. However, paternal inheritance, reduced effective population size, and lack of independence between loci can reduce Y-STR diversity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7939efde1cea58a523f63765ecc323cd
https://doi.org/10.1007/s00414-011-0568-3
https://doi.org/10.1007/s00414-011-0568-3
Publikováno v:
Cytogenetic and Genome Research. 81:213-216
Gene specific PCR primers were constructed for five mouse and three bovine CXC chemokine genes. The mouse genes were assigned using SSCP analyses of the Jackson BSS backcross panel to two groups on chromosome 5. One group containing Gro1 and Mip2 cos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93568135b04d0cc9e0ee8c9c2ce36913
https://doi.org/10.1159/000015033
https://doi.org/10.1159/000015033
Autor:
Abirami Chidambaram, Mae R. Gailani, Allen E. Bale, Bernard Gerrard, Michael Dean, Claudia Stewart, Alisa M. Goldstein, Ilya Chumakov
Publikováno v:
Genes, Chromosomes and Cancer. 18:212-218
Gorlin's syndrome or nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by a familial or hereditary predisposition to basal cell carcinomas (generally multiple and of early onset), odontogenic keratocysts (ja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dbdeb6ca99a09feb36a4f05a753085d
https://doi.org/10.1002/(sici)1098-2264(199703)18:3<212::aid-gcc7>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199703)18:3<212::aid-gcc7>3.0.co
Autor:
Abirami Chidambaram, Patrick D. Storto, Susanne M. Gollin, Janice A. Washington, Partrick S. Malone, Leon Barnes, Ivo P. Janecka
Publikováno v:
Genes, Chromosomes and Cancer. 4:146-152
Cytogenetic analysis of a cemento-ossifying fibroma from a patient with nonfamilial bilateral multicentric retinoblastoma revealed three reciprocal translocations with the karyotype 46,XY,t(1;18)(q21;q21.3),t(3;10)(p13;q22),t(6;11)(p22;p15). Routine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::300d27f0648ea36264fca983055e956b
https://doi.org/10.1002/gcc.2870040208
https://doi.org/10.1002/gcc.2870040208
Autor:
Bruce Budowle, Leanne Strickland, Abirami Chidambaram, Ranajit Chakraborty, Chris W Beheim, George M Taft
Publikováno v:
Forensic science international. 129(1)
Allele distributions for 13 short tandem repeat (STR) loci D3S1358, vWA, FGA, D8S1179, D21S11, D18S51, D5S818, D13S317, D7S820, TH01, TPOX, CSF1PO and D16S539 were determined for three Native Alaskan population groups—Athabaskans, Inupiats, and Yup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65022631195283e8c9f61dbcafb7d18d
https://pubmed.ncbi.nlm.nih.gov/12230997
https://pubmed.ncbi.nlm.nih.gov/12230997
Autor:
Abirami Chidambaram, Jeffery P. Struewing, Mary C. Fraser, Alisa M. Goldstein, Margaret A. Tucker
Publikováno v:
Journal of the National Cancer Institute. 92(12)
Background Two genes have been implicated in the development of cutaneous malignant melanoma (CMM). CDK4 (the gene encoding cyclin-dependent kinase 4, an oncogene) has exhibited germline mutations found in only three melanoma-prone families to date.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd1b053651665a72a79ee1c37f4d9c75
https://pubmed.ncbi.nlm.nih.gov/10861313
https://pubmed.ncbi.nlm.nih.gov/10861313
Autor:
Bernard Gerrard, Abirami Chidambaram, Siradanahalli C. Guru, Rando Allikmets, S. Chandrasekarappa, Michael Dean, William S. Modi
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 8(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427714f8e717f26902968dfc736b855d
https://pubmed.ncbi.nlm.nih.gov/9383297
https://pubmed.ncbi.nlm.nih.gov/9383297
Autor:
J. T. Feltis, Hiltrud Brauch, Gladys Glenn, C. Casadevall, McClellan M. Walther, Stefan Storkel, Thomas Stackhouse, Irina A. Lubensky, Ulf S.R. Bergerheim, C. J. M. Lips, Abirami Chidambaram, L. Slife, Peter L. Choyke, Rando Allikmets, B. Zbar, Holger Moch, Stéphane Richard, Lap-Chee Tsui, W.M. Linehan, Laura S. Schmidt, Zhengping Zhuang, Michael Dean, Jochen Decker, J. Lipan, M. Bernues, Fuh Mei Duh, Michael I. Lerman, A. Zamarron, Laura Geil, G. Niehans, Mary Lou Orcutt, Takeshi Kishida, Stephen W. Scherer, M. D. Hughson, F. Chen
Publikováno v:
Nature genetics. 16(1)
Hereditary papillary renal carcinoma (HPRC) is a recently recognized form of inherited kidney cancer characterized by a predisposition to develop multiple, bilateral papillary renal tumours. The pattern of inheritance of HPRC is consistent with autos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ef07a943329c273cbab5ba5bd4649a8
https://pubmed.ncbi.nlm.nih.gov/9140397
https://pubmed.ncbi.nlm.nih.gov/9140397
Autor:
Kent L. Anderson, Amy Hutchinson, Jeremy Nathans, Noah F. Shroyer, Amir Rattner, Mark Leppert, Bernard Gerrard, Abirami Chidambaram, James R. Lupski, Dora Stauffer, Yixin Li, Lisa Baird, Hui Sun, Philip M. Smallwood, Rando Allikmets, Richard A. Lewis, Michael Dean, Nanda A. Singh, Andy Peiffer
Publikováno v:
Nature genetics. 15(3)
Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2186b3ed42d96a86d1a632381b6c26eb
https://pubmed.ncbi.nlm.nih.gov/9425888
https://pubmed.ncbi.nlm.nih.gov/9425888