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Cell cycle regulation of the BRCA1/acetyl-CoA-carboxylase complex

Biochemical and biophysical research communications, 2009-01, Vol.378 (3), p.615-619

2009

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Evidence That Red Blood Cell Protein p55 May Participate in the Skeleton-Membrane Linkage That Involves Protein 4.1 and Glycophorin C

Blood, 1993-08, Vol.82 (4), p.1323-1327

1993

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A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

Blood, 1998-06, Vol.91 (11), p.4361-4367

1998

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719 Conjugation of endogenous BRCA1 protein with SUMO-2/3 is cell cycle-dependent

European journal of cancer supplements, 2010, Vol.8 (5), p.181-182

2010

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BRCA1 Affects Lipid Synthesis through Its Interaction with Acetyl-CoA Carboxylase

The Journal of biological chemistry, 2006-02, Vol.281 (6), p.3172-3181

2006

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Abnormal expression of protein 4.1 in spermatozoa of infertile men with teratospermia

The Lancet (British edition), 1994-03, Vol.343 (8900), p.764-765

1994

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Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Blood, 2000-03, Vol.95 (5), p.1834-1841

2000

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Constitutive Association of BRCA1 and c-Abl and Its ATM-Dependent Disruption after Irradiation

Molecular and Cellular Biology, 2002-06, Vol.22 (12), p.4020-4032

2002

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Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

The Journal of clinical investigation, 1992-11, Vol.90 (5), p.1713-1717

1992

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Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton

The Journal of clinical investigation, 1994-10, Vol.94 (4), p.1651-1656

1994

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A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

Blood, 1998-06, Vol.91 (11), p.4361-4367

1998

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A Dde I RFLP in Exon 21 of Human EL1 Gene, Encoding Protein 4.1, Detectable by SSCP

Human mutation, 1998, Vol.11 (4), p.342-343

1998

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Isolation of an enzyme catalysing nitrosamine formation in Pseudomonas aeruginosa and Neisseria mucosae

Biochemical and biophysical research communications, 1990-09, Vol.171 (2), p.655-660

1990

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Elliptopoikilocytosis Associated With the α469 His → Pro Mutation in Spectrin Barcelona (αI/50-46b)

Blood, 1993-09, Vol.82 (5), p.1661-1665

1993

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Production of polyclonal and monoclonal antibodies for specific detection of nitrosation-proficient denitrifying bacteria in biological fluids

Biochemical and biophysical research communications, 1991-04, Vol.176 (1), p.262-268

1991

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Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

Blood, 1993-08, Vol.82 (4), p.1323-1327

1993

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BRCA1 expression during prenatal development of the human mammary gland

Oncogene, 1999-07, Vol.18 (27), p.4039-4043

1999

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Differential expression and subcellular localization of murine BRCA1 and BRCA1-delta 11 isoforms in murine and human cell lines

International journal of cancer, 2000-11, Vol.88 (4), p.519-524

2000

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A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon

Human mutation, 1999, Vol.14 (2), p.145-155

1999

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Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis

Annales de génétique, 1996, Vol.39 (4), p.209

1996

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Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Blood, 2000 (95), p.1834-1841

2000

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Effects of anti-alpha monoclonal antibodies on initiation and elongation by the Escherichia coli RNA polymerase

The Journal of biological chemistry, 1990-05, Vol.265 (14), p.8122-8126

1990

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Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

Blood, 1993-09, Vol.82 (5), p.1661-1665

1993

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An α-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the αV/41 polymorphism

Human genetics, 1993-02, Vol.90 (6), p.641-644

1993

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Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

Blood, 1993-09, Vol.82 (5), p.1661-1665

1993

Volltextzugriff (PDF)

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Cell cycle regulation of the BRCA1/acetyl-CoA-carboxylase complex

Evidence That Red Blood Cell Protein p55 May Participate in the Skeleton-Membrane Linkage That Involves Protein 4.1 and Glycophorin C

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

719 Conjugation of endogenous BRCA1 protein with SUMO-2/3 is cell cycle-dependent

BRCA1 Affects Lipid Synthesis through Its Interaction with Acetyl-CoA Carboxylase

Abnormal expression of protein 4.1 in spermatozoa of infertile men with teratospermia

Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Constitutive Association of BRCA1 and c-Abl and Its ATM-Dependent Disruption after Irradiation

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

A Dde I RFLP in Exon 21 of Human EL1 Gene, Encoding Protein 4.1, Detectable by SSCP

Isolation of an enzyme catalysing nitrosamine formation in Pseudomonas aeruginosa and Neisseria mucosae

Elliptopoikilocytosis Associated With the α469 His → Pro Mutation in Spectrin Barcelona (αI/50-46b)

Production of polyclonal and monoclonal antibodies for specific detection of nitrosation-proficient denitrifying bacteria in biological fluids

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C

BRCA1 expression during prenatal development of the human mammary gland

Differential expression and subcellular localization of murine BRCA1 and BRCA1-delta 11 isoforms in murine and human cell lines

A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon

Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis

Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structure

Effects of anti-alpha monoclonal antibodies on initiation and elongation by the Escherichia coli RNA polymerase

Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

An α-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the αV/41 polymorphism

Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b)

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