UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation

Nature communications, 2022-11, Vol.13 (1), p.6641-6641, Article 6641

2022

Volltextzugriff (PDF)

Alpha Thalassaemias

Cellular and molecular life sciences : CMLS, 2009-04, Vol.66 (7), p.1154-1162

2009

Volltextzugriff (PDF)

Variable cells with identical genetic codes

Blood, 2020-05, Vol.135 (22), p.1921-1922

2020

Volltextzugriff (PDF)

Mutations in ATRX , encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

Nature genetics, 2000-04, Vol.24 (4), p.368-371

2000

Volltextzugriff (PDF)

Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

Blood, 2000, Vol.95 (1), p.360-362

2000

Volltextzugriff (PDF)

Localization of a Putative Transcriptional Regulator (ATRX) at Pericentromeric Heterochromatin and the Short Arms of Acrocentric Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1999-11, Vol.96 (24), p.13983-13988

1999

Volltextzugriff (PDF)

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

Haematologica (Roma), 2013-09, Vol.98 (9), p.1383-1387

2013

Volltextzugriff (PDF)

The Pattern of Replication at a Human Telomeric Region (16p13.3): Its Relationship to Chromosome Structure and Gene Expression

Human molecular genetics, 1999-08, Vol.8 (8), p.1373-1386

1999

Volltextzugriff (PDF)

Understanding α-Globin Gene Regulation: Aiming to Improve the Management of Thalassemia

Annals of the New York Academy of Sciences, 2005-11, Vol.1054 (1), p.92-102

2005

Volltextzugriff (PDF)

ATRX Encodes a Novel Member of the SNF2 Family of Proteins: Mutations Point to a Common Mechanism Underlying the ATR-X Syndrome

Human molecular genetics, 1996-12, Vol.5 (12), p.1899-1907

1996

Volltextzugriff (PDF)

A Review of the Molecular Genetics of the Human α-Globin Gene Cluster

Blood, 1989-04, Vol.73 (5), p.1081-1104

1989

Volltextzugriff (PDF)

Healing of broken human chromosomes by the addition of telomeric repeats

American journal of human genetics, 1994-09, Vol.55 (3), p.505-512

1994

Volltextzugriff (PDF)

Sequence Comparison of Human and Yeast Telomeres Identifies Structurally Distinct Subtelomeric Domains

Human molecular genetics, 1997-08, Vol.6 (8), p.1305-1314

1997

Volltextzugriff (PDF)

The relationship between chromosome structure and function at a human telomeric region

Nature genetics, 1997-03, Vol.15 (3), p.252-257

1997

Volltextzugriff (PDF)

A major positive regulatory region located far upstream of the human α-globin gene locus

Genes & development, 1990-09, Vol.4 (9), p.1588-1601

1990

Volltextzugriff (PDF)

Simplified multiplex-PCR diagnosis of common southeast Asian deletional determinants of α-thalassemia

Clinical chemistry (Baltimore, Md.), 2000-10, Vol.46 (10), p.1692-1695

2000

Volltextzugriff (PDF)

Recombination at the human α-globin gene cluster: Sequence features and topological constraints

Cell, 1987-05, Vol.49 (3), p.369-378

1987

Volltextzugriff (PDF)

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy

Annals of neurology, 2000-01, Vol.47 (1), p.117-121

2000

Volltextzugriff (PDF)

Cis-acting sequences regulating expression of the human α-globin cluster lie within constitutively open chromatin

Cell, 1992-05, Vol.69 (5), p.781-793

1992

Volltextzugriff (PDF)

Phenotype/genotype relationships in sickle cell disease: a pilot twin study

Clinical and laboratory haematology, 2005-12, Vol.27 (6), p.384-390

2005

Volltextzugriff (PDF)

A PCR‐based strategy to detect the common severe determinants of α thalassaemia

British journal of haematology, 1992-05, Vol.81 (1), p.104-108

1992

Volltextzugriff (PDF)

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Nature (London), 1985-10, Vol.317 (6037), p.542-544

1985

Volltextzugriff (PDF)

Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

Molecular and Cellular Biology, 1991-09, Vol.11 (9), p.4679-4689

1991

Volltextzugriff (PDF)

Nuclear scaffold attachment sites in the human globin gene complexes

The EMBO journal, 1988-11, Vol.7 (11), p.3337-3344

1988

Volltextzugriff (PDF)

Benign clinical course in homozygous sickle cell disease: A search for predictors

Journal of clinical epidemiology, 1997-02, Vol.50 (2), p.121-126

1997

Volltextzugriff (PDF)

1 – 25 von 848

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(763)
Mit Volltextzugriff
(646)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(534)
Life Sciences & Biomedicine
(441)
Humans
(374)
Biological And Medical Sciences
(208)
Female
(163)
Male
(160)
Animals
(149)
Medical Sciences
(127)
Globins - Genetics
(126)
Adult
(95)
Fundamental And Applied Biological Sciences. Psychology
(86)
Thalassemia - Genetics
(77)
Biochemistry & Molecular Biology
(67)
Genes
(64)
Middle Aged
(64)
Physical Sciences
(61)
Base Sequence
(58)
Mice
(57)
Hematology
(56)
Molecular Sequence Data
(56)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation

Alpha Thalassaemias

Variable cells with identical genetic codes

Mutations in ATRX , encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

Localization of a Putative Transcriptional Regulator (ATRX) at Pericentromeric Heterochromatin and the Short Arms of Acrocentric Chromosomes

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

The Pattern of Replication at a Human Telomeric Region (16p13.3): Its Relationship to Chromosome Structure and Gene Expression

Understanding α-Globin Gene Regulation: Aiming to Improve the Management of Thalassemia

ATRX Encodes a Novel Member of the SNF2 Family of Proteins: Mutations Point to a Common Mechanism Underlying the ATR-X Syndrome

A Review of the Molecular Genetics of the Human α-Globin Gene Cluster

Healing of broken human chromosomes by the addition of telomeric repeats

Sequence Comparison of Human and Yeast Telomeres Identifies Structurally Distinct Subtelomeric Domains

The relationship between chromosome structure and function at a human telomeric region

A major positive regulatory region located far upstream of the human α-globin gene locus

Simplified multiplex-PCR diagnosis of common southeast Asian deletional determinants of α-thalassemia

Recombination at the human α-globin gene cluster: Sequence features and topological constraints

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy

Cis-acting sequences regulating expression of the human α-globin cluster lie within constitutively open chromatin

Phenotype/genotype relationships in sickle cell disease: a pilot twin study

A PCR‐based strategy to detect the common severe determinants of α thalassaemia

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

Nuclear scaffold attachment sites in the human globin gene complexes

Benign clinical course in homozygous sickle cell disease: A search for predictors

Suchergebnisse filtern