Lista de obras - David F. Callen - Dominio Público Uruguay

A comparison of vitamin D activity in paired non-malignant and malignant human breast tissues

artículo científico publicado en 2012

A complex translocation in acute promyelocytic leukemia

article

A der(11)t(8;11) in two medulloblastomas. A possible nonrandom cytogenetic abnormality

artículo científico publicado en 1989

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect

artículo científico publicado en 2002

A human retinoblastoma cell line expressing the common acute lymphoblastic leukemia antigen and displaying an unusual chromosome abnormality

artículo científico publicado en 1986

A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplification

artículo científico publicado en 1998

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum

artículo científico publicado en 2001

A review of the t(1;19) breakpoints in acute lymphocytic leukemia

artículo científico publicado en 1985

A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies

artículo científico publicado en 1997

A template-based approach to inhibitors of calpain 2, 20S proteasome, and HIV-1 protease

artículo científico publicado en 2013

ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1.

artículo científico publicado en 1988

ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors

artículo científico publicado en 1998

Aberrant CBFA2T3B gene promoter methylation in breast tumors

artículo científico publicado en 2004

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1

article

Alternative Interpretation of Reported Paracentric Inversion ⬇️

artículo científico publicado el 1 de julio de 1998

An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15

article

Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene

article

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development

artículo científico

Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13

artículo científico publicado en 1997

Association of familial duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22

article

CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population

artículo científico publicado en 2003

CBFA2T3-ZNF651, like CBFA2T3-ZNF652, functions as a transcriptional corepressor complex

artículo científico publicado en 2010

CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB.

artículo científico publicado en 2008

Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

artículo científico publicado en 1998

Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

artículo científico publicado en 2014

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

article

Chromosomal analysis in ewing sarcoma

artículo científico publicado en 1987

Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidney.

artículo científico publicado en 1994

Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

article

Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14.

artículo científico publicado en 1988

Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen

artículo científico publicado en 1983

Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene ⬇️

artículo científico publicado el 1 de febrero de 1998

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.

artículo científico publicado en 1997

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

artículo científico publicado en 1998

Defining regions of loss of heterozygosity of 16q in breast cancer cell lines

scientific article published on 01 February 2002

Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphoma

artículo científico publicado en 2010

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

artículo científico publicado en 1987

Development of a novel cell-based assay system EPISSAY for screening epigenetic drugs and liposome formulated decitabine.

artículo científico publicado en 2013

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood

artículo científico publicado en 2015

Evaluation of a cosmid contig physical map of human chromosome 16

artículo científico publicado el 1 de agosto de 1992

Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis

artículo científico publicado en 2007

FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex

artículo científico publicado en 2005

Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

artículo científico publicado en 1993

Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16

article

Genome-wide mapping of ZNF652 promoter binding sites in breast cancer cells

artículo científico publicado en 2011

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3

artículo científico publicado en 1997

Giant axonal neuropathy locus refinement to a < 590 kb critical interval

artículo científico publicado en 2000

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome

artículo científico publicado en 1997

High-resolution cytogenetic-based physical map of human chromosome 16.

artículo científico publicado en 1992

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

artículo científico publicado en 2010

Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites

artículo científico publicado en 1991

Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences

artículo científico publicado en 1989

Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13.

artículo científico publicado en 1993

Identification of ANKRD11 as a p53 coactivator

artículo científico publicado en 2008

Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.

artículo científico publicado en 2011

Inhibition of DNA-dependent protein kinase induces accelerated senescence in irradiated human cancer cells

artículo científico publicado en 2011

Integration of cytogenetic landmarks into the draft sequence of the human genome

artículo científico publicado en 2001

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.

artículo científico publicado en 1995

Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss

artículo científico publicado en 1983

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15

scientific article published on 01 August 1988

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

artículo científico publicado en 1992

Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16

scientific journal article

Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening

article

Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity

artículo científico publicado en 1998

Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

artículo científico publicado en 1990

Localization of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels

artículo científico publicado en 1998

Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease

article

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site

artículo científico publicado en 1991

Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.

artículo científico publicado en 1991

Mapping the short arm of human chromosome 16.

artículo científico publicado en 1989

Mechanistic Insight into Cell Growth, Internalization, and Cytotoxicity of PAMAM Dendrimers

artículo científico publicado en 2010

Molecular analysis of human chromosome 16 cosmid clones containing NotI sites

artículo científico publicado en 1992

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein

artículo científico publicado en 2001

Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1

artículo científico publicado en 1995

Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)

artículo científico publicado en 1996

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

artículo científico publicado el 1 de julio de 1992

Mutant p53 drives invasion in breast tumors through up-regulation of miR-155.

artículo científico publicado en 2012

Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11.

artículo científico publicado en 2011

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.

artículo científico publicado en 1999

New 26S proteasome inhibitors with high selectivity for chymotrypsin-like activity and p53-dependent cytotoxicity

artículo científico publicado en 2012

New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia

scientific article published on 01 February 1991

New regional localisations for HAGH and PGP on human chromosome 16

artículo científico publicado en 1986

Nutlin-3a efficacy in sarcoma predicted by transcriptomic and epigenetic profiling

artículo científico publicado en 2013

Nutlin-3a is a potential therapeutic for ewing sarcoma

artículo científico publicado en 2010

Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

artículo científico publicado en 2004

Phenol sulfotransferases: candidate genes for Batten disease.

artículo científico publicado en 1995

Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3.

artículo científico publicado en 1993

Physical map of the region containing the gene for Batten disease (CLN3)

article

Pre-activation of the p53 pathway through Nutlin-3a sensitises sarcomas to drozitumab therapy

artículo científico publicado en 2013

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1

scientific article published on 01 February 1990

RCH-ACV: a lymphoblastic leukemia cell line with chromosome translocation 1;19 and trisomy 8.

artículo científico publicado en 1986

Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16

artículo científico publicado en 1993

Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.

artículo científico publicado en 1993

Reply to the letter to the editor by Partington and Turner??Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes?

article published in 1999

SCF-FBXO31 E3 ligase targets DNA replication factor Cdt1 for proteolysis in the G2 phase of cell cycle to prevent re-replication

artículo científico publicado en 2014

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes

artículo científico publicado en 2002

Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16

artículo científico publicado en 1993

Specific-site methylation of tumour suppressor ANKRD11 in breast cancer

artículo científico publicado en 2012

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies

artículo científico publicado en 2002

Synthesis and extended activity of triazole-containing macrocyclic protease inhibitors

artículo científico publicado en 2013

Systematic characterisation of the rat and human CYP24A1 promoter

artículo científico publicado en 2010

Targeting the p53 Pathway in Ewing Sarcoma.

artículo científico publicado en 2010

The application of delivery systems for DNA methyltransferase inhibitors

artículo científico publicado en 2011

The gene for human interleukin 7 (IL7) is at 8q12-13

artículo científico publicado en 1989

The gene for the human IgA Fc receptor maps to 19q13.4

artículo científico publicado en 1992

The genomic organization of the Fanconi anemia group A (FAA) gene

artículo científico publicado en 1997

The oncogenic role of miR-155 in breast cancer

artículo científico publicado en 2012

The sequence and analysis of duplication-rich human chromosome 16

artículo científico publicado en 2004

Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3

artículo científico publicado en 1988

Two RFLPs detected by a cosmid at locus D16S144.

artículo científico publicado en 1990

Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24

artículo científico publicado el 1 de enero de 1992

Within pair differences of human chromosome 9 C-bands associated with reproductive loss

artículo científico publicado en 1982

XI-006 induces potent p53-independent apoptosis in Ewing sarcoma

artículo científico publicado en 2015

YAC and Cosmid Contigs Spanning the Batten Disease (CLN3) Region at 16p12.1–p11.2

artículo científico publicado en 1995

ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription

artículo científico publicado en 2006

p53 Represses the Oncogenic Sno-MiR-28 Derived from a SnoRNA

artículo científico publicado en 2015

p53 continues to surprise: high levels of p53 can suppress apoptosis

artículo científico publicado en 2012

Lista de obras de David F. Callen

A comparison of vitamin D activity in paired non-malignant and malignant human breast tissues

A complex translocation in acute promyelocytic leukemia

A der(11)t(8;11) in two medulloblastomas. A possible nonrandom cytogenetic abnormality

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect

A human retinoblastoma cell line expressing the common acute lymphoblastic leukemia antigen and displaying an unusual chromosome abnormality

A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplification

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum

A review of the t(1;19) breakpoints in acute lymphocytic leukemia

A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies

A template-based approach to inhibitors of calpain 2, 20S proteasome, and HIV-1 protease

ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1.

ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors

Aberrant CBFA2T3B gene promoter methylation in breast tumors

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1

Alternative Interpretation of Reported Paracentric Inversion ⬇️

An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15

Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development

Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13

Association of familial duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22

CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population

CBFA2T3-ZNF651, like CBFA2T3-ZNF652, functions as a transcriptional corepressor complex

CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB.

Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

Chromosomal analysis in ewing sarcoma

Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidney.

Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14.

Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen

Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene ⬇️

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

Defining regions of loss of heterozygosity of 16q in breast cancer cell lines

Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphoma

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

Development of a novel cell-based assay system EPISSAY for screening epigenetic drugs and liposome formulated decitabine.

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood

Evaluation of a cosmid contig physical map of human chromosome 16

Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis

FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex

Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16

Genome-wide mapping of ZNF652 promoter binding sites in breast cancer cells

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3

Giant axonal neuropathy locus refinement to a < 590 kb critical interval

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome

High-resolution cytogenetic-based physical map of human chromosome 16.

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites

Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences

Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13.

Identification of ANKRD11 as a p53 coactivator

Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.

Inhibition of DNA-dependent protein kinase induces accelerated senescence in irradiated human cancer cells

Integration of cytogenetic landmarks into the draft sequence of the human genome

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.

Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16

Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening

Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity

Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

Localization of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels

Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site

Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.

Mapping the short arm of human chromosome 16.

Mechanistic Insight into Cell Growth, Internalization, and Cytotoxicity of PAMAM Dendrimers

Molecular analysis of human chromosome 16 cosmid clones containing NotI sites

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein

Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

Mutant p53 drives invasion in breast tumors through up-regulation of miR-155.

Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11.

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.