Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tala Shahlavi"'
Autor:
Edythe Wiggs, Carl C. Baker, Deborah Tamura, Kenneth H. Kraemer, Chris Zalewski, Tala Shahlavi, Steffen Emmert, John J. DiGiovanna, Kyu-Seon Oh, Raphael Schiffmann, Marcy Neuburg, Carmen C. Brewer, Kyoko Imoto, Najealicka Armstrong, Sikandar G. Khan
Publikováno v:
DNA Repair. 8:114-125
Two unrelated xeroderma pigmentosum (XP) patients, with and without neurological abnormalities, respectively, had identical defects in the XPC DNA nucleotide excision repair (NER) gene. Patient XP21BE, a 27-year-old woman, had developmental delay and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10468735caad1c8aa402f65f2fd617b4
https://doi.org/10.1016/j.dnarep.2008.09.007
https://doi.org/10.1016/j.dnarep.2008.09.007
Autor:
Myung-Moo Lee, Steffen Emmert, Roberta Bliss Albert, John J. DiGiovanna, David B. Busch, Jill Crollick, Bassam Abu-Libdeh, Sikandar G. Khan, Hanoch Slor, Takahiro Ueda, Sima Batko, Donna M. Coleman, Bari B. Cunningham, Lawrence Grossman, Kenneth H. Kraemer, Mohammad Hedayati, James E. Cleaver, Hiroki Inui, Tala Shahlavi
Publikováno v:
Journal of Investigative Dermatology. 118:972-982
We studied three newly diagnosed xeroderma pigmentosum complementation group G patients with markedly different clinical features. An Israeli-Palestinian girl (XP96TA) had severe abnormalities suggestive of the xeroderma pigmentosum/Cockayne syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a0a803677abd6c18e1e20e274a26537
https://doi.org/10.1046/j.1523-1747.2002.01782.x
https://doi.org/10.1046/j.1523-1747.2002.01782.x
Autor:
Alain Sarasin, Ahmet Metin, Kyoko Imoto, Hiroki Inui, Carl C. Baker, David B. Busch, Kenneth H. Kraemer, Arash Khadavi, Steffen Emmert, Tala Shahlavi, Hanoch Slor, John J. DiGiovanna, Deborah Schmidt, Engin M. Gozukara, Sikandar G. Khan, Takahiro Ueda, Vanessa Muniz-Medina, Kyu-Seon Oh
Publikováno v:
Carcinogenesis. 27(1)
Xeroderma pigmentosum group C (XP-C) is a rare autosomal recessive disorder. Patients with two mutant alleles of the XPC DNA repair gene have sun sensitivity and a 1000-fold increase in skin cancers. Clinically normal parents of XP-C patients have on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c906449794a369c873a7fd3457071f4c
https://pubmed.ncbi.nlm.nih.gov/16081512
https://pubmed.ncbi.nlm.nih.gov/16081512
Autor:
Sikandar G. Khan, Ahmet Metin, Thomas D. Schneider, Kenneth H. Kraemer, Engin M. Gozukara, Tala Shahlavi, Takahiro Ueda, Vanessa Muniz-Medina, Hiroki Inui, Juliet R. Aiken, Carl C. Baker
The lariat branch point sequence (BPS) is crucial for splicing of human nuclear pre-mRNA yet BPS mutations have infrequently been reported to cause human disease. Using an inverse RT-PCR technique we mapped two BPS to the adenosine residues at positi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02167f3c52b8e3bbef5a8fe1b6600ed
https://avesis.yyu.edu.tr/publication/details/80f24934-deeb-4f49-96f0-663896953198/oai
https://avesis.yyu.edu.tr/publication/details/80f24934-deeb-4f49-96f0-663896953198/oai
Autor:
Sikandar G. Khan, Kyu-Seon Oh, Tala Shahlavi, Takahiro Ueda, David B. Busch, Hiroki Inui, Steffen Emmert, Kyoko Imoto, Vanessa Muniz-Medina, Carl C. Baker, John J. DiGiovanna, Deborah Schmidt, Arash Khadavi, Ahmet Metin, Engin Gozukara, Hanoch Slor, Alain Sarasin, Kenneth H. Kraemer
Publikováno v:
Carcinogenesis; Jan2006, Vol. 27 Issue 1, p84-94, 11p
Autor:
David B. Busch, Ahmet Metin, Donna M. Coleman, Mark Steven Miller, Engin M. Gozukara, Steffen Emmert, Nonglux Chinsomboon, Kenneth H. Kraemer, Tala Shahlavi, Sikandar G. Khan, Miria Stefanini
Publikováno v:
Journal of Investigative Dermatology. (2):197-204
Xeroderma pigmentosum family G from Van, Turkey had two severely affected children: a son with multiple skin cancers who died at age 10 (XP67TMA), and an 8 y old daughter who began developing skin cancer before 3 y of age (XP68TMA). XP67TMA and XP68T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21a88c1a12779dcc67c9aab233a08dc7