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Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites

Oncogene, 2006-07, Vol.25 (32), p.4381-4388

2006

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Genomic amplification of MET with boundaries within fragile site FRA7G and upregulation of MET pathways in esophageal adenocarcinoma

Oncogene, 2006-01, Vol.25 (3), p.409-418

2006

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Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome

Nature (London), 2003-05, Vol.423 (6937), p.293-298

2003

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Common fragile sites

Cytogenetic and Genome Research, 2003-01, Vol.100 (1-4), p.92-100

2003

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Replication of a Common Fragile Site, FRA3B, Occurs Late in S Phase and is Delayed Further Upon Induction: Implications for the Mechanism of Fragile Site Induction

Human molecular genetics, 1998-04, Vol.7 (4), p.755-761

1998

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FRA3B Extends Over a Broad Region and Contains a Spontaneous HPV16 Integration Site: Direct Evidence for the Coincidence of Viral Integration Sites and Fragile Sites

Human molecular genetics, 1996-02, Vol.5 (2), p.187-195

1996

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Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

Journal of medical genetics, 2001-11, Vol.38 (11), p.761-766

2001

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Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients

Nature (London), 1992-04, Vol.356 (6371), p.713-715

1992

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ATR Regulates Fragile Site Stability

Cell, 2002-12, Vol.111 (6), p.779-789

2002

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A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito

Nature genetics, 1996-07, Vol.13 (3), p.361-365

1996

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Temperature gradients due to adiabatic plasma expansion in a magnetic nozzle

Plasma sources science & technology, 2014-08, Vol.23 (4), p.45014-7

2014

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Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas

Oncogene, 1997-10, Vol.15 (14), p.1653-1659

1997

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A Novel Frameshift Mutation in Exon 23 of ATP7A ( MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease

American journal of human genetics, 2001-08, Vol.69 (2), p.420-427

2001

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A minimal critical region of the 8p22-23 amplicon in esophageal adenocarcinomas defined using sequence tagged site-amplification mapping and quantitative polymerase chain reaction includes the GATA-4 gene

Cancer research (Chicago, Ill.), 2000-03, Vol.60 (5), p.1341-1347

2000

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Observations of single-pass ion cyclotron heating in a trans-sonic flowing plasma

Physics of plasmas, 2010-04, Vol.17 (4), p.043509-043509-19

2010

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Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

American journal of human genetics, 2000-12, Vol.67 (6), p.1382-1388

2000

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Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux

Human molecular genetics, 1995-11, Vol.4 (11), p.2117-2123

1995

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Isolation of human and murine homologues of the Drosophila minibrain gene : Human homologue maps to 21q22.2 in the Down syndrome critical region

Genomics (San Diego, Calif.), 1996-12, Vol.38 (3), p.331-339

1996

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Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans-Golgi Network

Human molecular genetics, 1997-03, Vol.6 (3), p.409-416

1997

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Distinct areas of allelic loss on chromosomal regions 10p and 10q in human prostate cancer

Cancer research (Chicago, Ill.), 1996-05, Vol.56 (10), p.2263-2267

1996

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Chromosome breakage and recombination at fragile sites

American journal of human genetics, 1988-09, Vol.43 (3), p.265-273

1988

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The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region

Cancer research (Chicago, Ill.), 1998-08, Vol.58 (15), p.3409-3414

1998

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Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors

Cancer research (Chicago, Ill.), 1996-10, Vol.56 (19), p.4347-4350

1996

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Positional Cloning of the Hereditary Renal Carcinoma 3;8 Chromosome Translocation Breakpoint

Proceedings of the National Academy of Sciences - PNAS, 1993-09, Vol.90 (18), p.8509-8513

1993

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Induction of sister chromatid exchanges at common fragile sites

American journal of human genetics, 1987-11, Vol.41 (5), p.882-890

1987

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Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites

Genomic amplification of MET with boundaries within fragile site FRA7G and upregulation of MET pathways in esophageal adenocarcinoma

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome

Common fragile sites

Replication of a Common Fragile Site, FRA3B, Occurs Late in S Phase and is Delayed Further Upon Induction: Implications for the Mechanism of Fragile Site Induction

FRA3B Extends Over a Broad Region and Contains a Spontaneous HPV16 Integration Site: Direct Evidence for the Coincidence of Viral Integration Sites and Fragile Sites

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients

ATR Regulates Fragile Site Stability

A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito

Temperature gradients due to adiabatic plasma expansion in a magnetic nozzle

Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas

A Novel Frameshift Mutation in Exon 23 of ATP7A ( MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease

A minimal critical region of the 8p22-23 amplicon in esophageal adenocarcinomas defined using sequence tagged site-amplification mapping and quantitative polymerase chain reaction includes the GATA-4 gene

Observations of single-pass ion cyclotron heating in a trans-sonic flowing plasma

Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux

Isolation of human and murine homologues of the Drosophila minibrain gene : Human homologue maps to 21q22.2 in the Down syndrome critical region

Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans-Golgi Network

Distinct areas of allelic loss on chromosomal regions 10p and 10q in human prostate cancer

Chromosome breakage and recombination at fragile sites

The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region

Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors

Positional Cloning of the Hereditary Renal Carcinoma 3;8 Chromosome Translocation Breakpoint

Induction of sister chromatid exchanges at common fragile sites

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