David B. Busch

Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients (2006)

Khan, Sikandar G., Oh, Kyu-Seon, Shahlavi, Tala, Ueda, Takahiro, Busch, David B., Inui, Hiroki, ...

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....

Reduced XPC DNA repair gene mRNA levels in clinically normal arents of xeroderma pigmentosum patients (2005)

Khan, Sikandar G., Oh, Kyu-Seon, Shahlavi, Tala, Ueda, Takahiro, Busch, David B., Inui, Hiroki, ...

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....

Reduced XPC DNA repair gene mRNA levels in clinically normal arents of xeroderma pigmentosum patients (2005)

Khan, Sikandar G., Oh, Kyu-Seon, Shahlavi, Tala, Ueda, Takahiro, Busch, David B., Inui, Hiroki, ...

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....

Human cells with multiple monosomies. An overlooked resource for readily isolating cells with autosomal recessive mutations? (1989)

Busch, David B.

The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells

Liu, Nan, Lamerdin, Jane E., Tucker, James D., Zhou, Zi-Q., Walter, Christi A., Albala, Joanna S., ...

The Chinese hamster ovary (CHO) mutant UV40 cell line is hypersensitive to UV and ionizing radiation, simple alkylating agents, and DNA cross-linking agents. The mutant cells also have a high level...

Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

Meira, Lisiane B., Greenberg, Cheryl R., Busch, David B., Doughty, Ana T. B., Ziffer, Deborah W., ...

Cerebro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to brain atrophy with calcification, cataracts, microcornea, optic atrophy, progressive joint...

The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells

Liu, Nan, Lamerdin, Jane E., Tucker, James D., Zhou, Zi-Q., Walter, Christi A., Albala, Joanna S., ...

The Chinese hamster ovary (CHO) mutant UV40 cell line is hypersensitive to UV and ionizing radiation, simple alkylating agents, and DNA cross-linking agents. The mutant cells also have a high level...

Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

Meira, Lisiane B., Greenberg, Cheryl R., Busch, David B., Doughty, Ana T. B., Ziffer, Deborah W., ...

Cerebro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to brain atrophy with calcification, cataracts, microcornea, optic atrophy, progressive joint...