T. Ueda

发表

Transcription-coupled nucleotide excision repair as a determinant of cisplatin sensitivity of human cells.

Y. Pommier, A. Sarasin, T. Furuta, 2002, Cancer research.

Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer‐prone xeroderma pigmentosum vs. non‐cancer‐prone trichothiodystrophy

Sikandar G. Khan, J. Jagdeo, T. Ueda, 2008, Human mutation.

Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.

Sikandar G. Khan, H. Inui, A. Sarasin, 2006, Carcinogenesis.

The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function.

T. D. Schneider, Sikandar G. Khan, H. Inui, 2002, Nucleic acids research.

Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum

Sikandar G. Khan, M. Tucker, A. Goldstein, 2012, European Journal of Human Genetics.

Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk.

Hiroki Inui, T. D. Schneider, Juliet R. Aiken, 2003, Human molecular genetics.

Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Sikandar G. Khan, K. Lachlan, A. Lehmann, 2006, Human mutation.

Ocular manifestations of xeroderma pigmentosum: long-term follow-up highlights the role of DNA repair in protection from sun damage.

Sikandar G. Khan, J. Clayton, H. Inui, 2013, Ophthalmology.

Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.

Sikandar G. Khan, H. Inui, L. Grossman, 2002, The Journal of investigative dermatology.

Formation of Cyclobutane Pyrimidine Dimers and 8-Oxo-7,8-dihydro-2′-deoxyguanosine in Mouse and Organ-cultured Human Skin by Irradiation with Broadband or with Narrowband UVB¶

M. Ueda, M. Ichihashi, T. Ueda, 2002, Photochemistry and photobiology.

Chimeric Negative Regulation of p14ARF and TBX1 by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency

Sikandar G. Khan, P. Meltzer, J. Butman, 2013, Human mutation.

The nucleosome‐binding protein HMGN2 modulates global genome repair

M. Bustin, T. Ueda, K. Kraemer, 2009, The FEBS journal.

Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients

J. Egly, T. Ueda, K. Kraemer, 2009, The Journal of experimental medicine.

A novel XPA gene mutation and its functional analysis in a Japanese patient with xeroderma pigmentosum group A.

T. Nagano, M. Ichihashi, T. Ueda, 2005, The Journal of investigative dermatology.

High‐risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies

Sikandar G. Khan, M. Tucker, A. Goldstein, 2011, Prenatal diagnosis.

Diagnostic difficulty in polycystic ovary syndrome due to an LH-beta-subunit variant.

T. Ueda, T. Ozaki, K. Takahashi, 1999, European journal of endocrinology.

Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum

Sikandar G. Khan, J. Egly, T. Ueda, 2012, European Journal of Human Genetics.

Ocular manifestations of trichothiodystrophy.

Sikandar G. Khan, J. Clayton, W. Zein, 2011, Ophthalmology.

A case of uterine lymphangioleiomyomatosis in a young woman that was identified via peritonitis

T. Ueda, M. Kuroda, S. Kawai, 2018, The journal of obstetrics and gynaecology research.

Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2)

Sikandar G. Khan, A. Bircher, T. Ueda, 2009, Experimental dermatology.

A further case of plantar squamous cell carcinoma arising in Olmsted syndrome

M. Ueda, M. Ichihashi, T. Ueda, 2001, The British journal of dermatology.

A Case of Oral Florid Papillomatosis (OFP) Successfully Treated with Intralesional Injection of IFN-α and Oral Etretinate

M. Ichihashi, T. Ueda, T. Kamo, 1996 .

Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair

Sikandar G. Khan, M. Tucker, A. Goldstein, 2010, Journal of Medical Genetics.

Heterozygous HPS1 mutations in a case of Hermansky–Pudlak syndrome with giant melanosomes

M. Ueda, M. Ichihashi, T. Horikawa, 2000, The British journal of dermatology.

Xeroderma pigmentosum-variant patients from America, Europe, and Asia.

Roger Woodgate, Hiroki Inui, Wen Hao Wu, 2008, The Journal of investigative dermatology.

Formation of Cyclobutane Pyrimidine Dimers and 8‐Oxo‐7,8‐dihydro‐2′‐deoxyguanosine in Mouse and Organ‐cultured Human Skin by Irradiation with Broadband or with Narrowband UVB ¶

M. Ueda, M. Ichihashi, T. Ueda, 2002 .

Ovarian clear cell adenocarcinoma revealed in a young patient during hormone therapy: a case report

T. Ueda, M. Kuroda, S. Kawai, 2016 .

Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair

Y. Pommier, S. Akiyama, D. Zimonjic, 2001, Nature Medicine.

Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development

J. Troendle, R. Moslehi, T. Ueda, 2010, Clinical genetics.

Delayed immune-related neutropenia with hepatitis by pembrolizumab.

M. Hino, T. Ueda, H. Koh, 2021, Immunotherapy.

Ocular manifestations of trichothiodystrophy.

Sikandar G. Khan, J. Clayton, W. Zein, 2011, Ophthalmology.

Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair

Sikandar G. Khan, M. Tucker, A. Goldstein, 2010, Journal of Medical Genetics.

Photosensitive dermatitis caused by pyridoxine hydrochloride.

N. Araki, T. Ueda, Y. Murata, 1998, Journal of the American Academy of Dermatology.