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...

Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e201-e209

2012

Volltextzugriff (PDF)

A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia

Leukemia, 2001-10, Vol.15 (10), p.1495-1504

2001

Volltextzugriff (PDF)

O-027 Small extracellular vesicle (sEV) protein cargo as potential biomarker for endometriosis

Human reproduction (Oxford), 2022-06, Vol.37 (Supplement_1)

2022

Volltextzugriff (PDF)

Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin

Journal of thrombosis and haemostasis, 2010-08, Vol.8 (8), p.1866-1868

2010

Volltextzugriff (PDF)

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Nature genetics, 1999-11, Vol.23 (3), p.296-303

1999

Volltextzugriff (PDF)

Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

American journal of human genetics, 2001-11, Vol.69 (5), p.1002-1012

2001

Volltextzugriff (PDF)

Comparative and integrated analysis of plasma extracellular vesicle isolation methods in healthy volunteers and patients following myocardial infarction

Journal of extracellular biology, 2022-11, Vol.1 (11), p.e66-n/a

2022

Volltextzugriff (PDF)

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Human molecular genetics, 2003-09, Vol.12 (18), p.2369-2378

2003

Volltextzugriff (PDF)

The chicken dystrophin cDNA: striking conservation of the C‐terminal coding and 3′ untranslated regions between man and chicken

The EMBO journal, 1988-12, Vol.7 (13), p.4157-4162

1988

Volltextzugriff (PDF)

An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi

Molecular microbiology, 2003-03, Vol.47 (6), p.1495-1512

2003

Volltextzugriff (PDF)

Isolated Dystrophin Molecules as Seen by Electron Microscopy

Proceedings of the National Academy of Sciences - PNAS, 1990-10, Vol.87 (20), p.7851-7855

1990

Volltextzugriff (PDF)

Prélèvements bactériologiques des surfaces : importance de l'étape d'enrichissement et du choix des milieux de culture

Annales de biologie clinique (Paris), 2005-09, Vol.63 (5), p.481-486

2005

Volltextzugriff (PDF)

The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis

Nucleic acids research, 2001-05, Vol.29 (10), p.2145-2153

2001

Volltextzugriff (PDF)

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Nature genetics, 1997-02, Vol.15 (2), p.157-164

1997

Volltextzugriff (PDF)

Bacterial Mode of Replication with Eukaryotic-Like Machinery in a Hyperthermophilic Archaeon

Science (American Association for the Advancement of Science), 2000-06, Vol.288 (5474), p.2212-2215

2000

Volltextzugriff (PDF)

Mutations in the gene encoding SLURP-1 in Mal de Meleda

Human molecular genetics, 2001-04, Vol.10 (8), p.875-880

2001

Volltextzugriff (PDF)

Rapid PCR analysis of the St14 (DXS52) VNTR

Nucleic acids research, 1991-04, Vol.19 (8), p.1944-1944

1991

Volltextzugriff (PDF)

Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2→q24.1 by in situ hybridization. Conserved and compared synteny between human and chicken

Cytogenetic and genome research, 2002, Vol.97 (3-4), p.234-238

2002

Volltextzugriff (PDF)

Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the [alpha]IIb[beta]3 integrin

Journal of thrombosis and haemostasis, 2010-08, Vol.8 (8), p.1866

2010

Volltextzugriff (PDF)

Premiers regards sur la séquence du génome humain

M.S. Médecine sciences, 2001, Vol.17 (3), p.299

2001

Volltextzugriff (PDF)

Characterization of the NPHP1 Locus: Mutational Mechanism Involved in Deletions in Familial Juvenile Nephronophthisis

American journal of human genetics, 2000-03, Vol.66 (3), p.778-789

2000

Volltextzugriff (PDF)

Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1

Human molecular genetics, 1997-12, Vol.6 (13), p.2247-2255

1997

Volltextzugriff (PDF)

Current Management of Idiopathic Clubfoot Questionnaire: A Multicentric Study

Journal of pediatric orthopaedics, 2003-11, Vol.23 (6), p.780-787

2003

Volltextzugriff (PDF)

An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

Human genetics, 1990-02, Vol.84 (3), p.283-285

1990

Volltextzugriff (PDF)

1 – 25 von 627

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(522)
Mit Volltextzugriff
(512)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(351)
Life Sciences & Biomedicine
(302)
Humans
(242)
Male
(154)
Biological And Medical Sciences
(143)
Animals
(138)
Female
(116)
Medical Sciences
(98)
Neurosciences
(79)
Adult
(76)
Rats
(72)
Neurosciences & Neurology
(70)
Medicin Och Hälsovetenskap
(61)
Middle Aged
(55)
Psychiatry
(55)
Fundamental And Applied Biological Sciences. Psychology
(53)
Biochemistry & Molecular Biology
(48)
Pharmacology & Pharmacy
(40)
Alcoholism
(35)
Molecular Sequence Data
(34)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients

A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia

O-027 Small extracellular vesicle (sEV) protein cargo as potential biomarker for endometriosis

Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

Comparative and integrated analysis of plasma extracellular vesicle isolation methods in healthy volunteers and patients following myocardial infarction

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

A candidate gene for familial Mediterranean fever

The chicken dystrophin cDNA: striking conservation of the C‐terminal coding and 3′ untranslated regions between man and chicken

An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi

Isolated Dystrophin Molecules as Seen by Electron Microscopy

Prélèvements bactériologiques des surfaces : importance de l'étape d'enrichissement et du choix des milieux de culture

The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Bacterial Mode of Replication with Eukaryotic-Like Machinery in a Hyperthermophilic Archaeon

Mutations in the gene encoding SLURP-1 in Mal de Meleda

Rapid PCR analysis of the St14 (DXS52) VNTR

Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2→q24.1 by in situ hybridization. Conserved and compared synteny between human and chicken

Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the [alpha]IIb[beta]3 integrin

Premiers regards sur la séquence du génome humain

Characterization of the NPHP1 Locus: Mutational Mechanism Involved in Deletions in Familial Juvenile Nephronophthisis

Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1

Current Management of Idiopathic Clubfoot Questionnaire: A Multicentric Study

An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

Suchergebnisse filtern