UB Paderborn / Katalog / Suche / in CDI

Es ist ein Fehler in der Kommunikation mit einem externen System aufgetreten. Bitte versuchen Sie Ihre letzte Aktion erneut. Sollte der Fehler bestehen bleiben, setzen Sie sich bitte mit dem Informationszentrum der Bibliothek in Verbindung oder versuchen Sie es später erneut.

1 – 25 von 2.406

Sortiert nach

Long-term degradation of optical devices on the Moon

Icarus (New York, N.Y. 1962), 2010-07, Vol.208 (1), p.31-35

2010

Volltextzugriff (PDF)

Laser ranging to the lost Lunokhod 1 reflector

Icarus (New York, N.Y. 1962), 2011-02, Vol.211 (2), p.1103-1108

2011

Volltextzugriff (PDF)

Mutations in EXPH5 result in autosomal recessive inherited skin fragility

British journal of dermatology (1951), 2014-01, Vol.170 (1), p.196-199

2014

Volltextzugriff (PDF)

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Nature genetics, 1997-10, Vol.17 (2), p.240-244

1997

Volltextzugriff (PDF)

Fifteen Years of Millimeter Accuracy Lunar Laser Ranging with APOLLO: Data Set Characterization

Publications of the Astronomical Society of the Pacific, 2023-10, Vol.135 (1052), p.104504

2023

Volltextzugriff (PDF)

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Muscle & nerve, 2007-01, Vol.35 (1), p.24-35

2007

Volltextzugriff (PDF)

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory

British journal of dermatology (1951), 2015-01, Vol.172 (1), p.94-100

2015

Volltextzugriff (PDF)

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Nature genetics, 1996-08, Vol.13 (4), p.450-457

1996

Volltextzugriff (PDF)

Beta defensin-3 engineered epidermis shows highly protective effect for bacterial infection

Gene therapy, 2005-05, Vol.12 (10), p.857-861

2005

Volltextzugriff (PDF)

APOLLO: millimeter lunar laser ranging

Classical and quantum gravity, 2012-09, Vol.29 (18), p.184005-11

2012

Volltextzugriff (PDF)

An absolute calibration system for millimeter-accuracy APOLLO measurements

Classical and quantum gravity, 2017-12, Vol.34 (24), p.245008

2017

Volltextzugriff (PDF)

Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma

British journal of dermatology (1951), 2008-04, Vol.158 (4), p.864-867

2008

Volltextzugriff (PDF)

Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family

British journal of dermatology (1951), 2015-05, Vol.172 (5), p.1407-1411

2015

Volltextzugriff (PDF)

Lunar eclipse observations reveal anomalous thermal performance of Apollo reflectors

Icarus (New York, N.Y. 1962), 2014-03, Vol.231, p.183-192

2014

Volltextzugriff (PDF)

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British journal of dermatology (1951), 2015-02, Vol.172 (2), p.527-531

2015

Volltextzugriff (PDF)

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

British journal of dermatology (1951), 2015-11, Vol.173 (5), p.1291-1294

2015

Volltextzugriff (PDF)

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition

The American journal of pathology, 1996-06, Vol.148 (6), p.1787-1796

1996

Volltextzugriff (PDF)

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

British journal of dermatology (1951), 1998-11, Vol.139 (5), p.767-775

1998

Volltextzugriff (PDF)

Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1

British journal of dermatology (1951), 1999-02, Vol.140 (2), p.297-307

1999

Volltextzugriff (PDF)

Gap junction development in the human fetal hair follicle and bulge region

British journal of dermatology (1951), 2004-03, Vol.150 (3), p.429-434

2004

Volltextzugriff (PDF)

The Apache Point Observatory Lunar Laser-ranging Operation (APOLLO) : Two Years of Millimeter-Precision Measurements of the Earth-Moon Range

Publications of the Astronomical Society of the Pacific, 2009, Vol.121 (875), p.29-40

2009

Volltextzugriff (PDF)

Dangerousness, mental disorder, and responsibility

Journal of medical ethics, 2003-08, Vol.29 (4), p.232-235

McMillan, J R

2003

Volltextzugriff (PDF)

NICE, the draft fertility guideline and dodging the big question

Journal of medical ethics, 2003-12, Vol.29 (6), p.313-314

McMillan, J R

2003

Volltextzugriff (PDF)

Hemidesmosomes Show Abnormal Association with the Keratin Filament Network in Junctional Forms of Epidermolysis Bullosa

Journal of investigative dermatology, 1998-02, Vol.110 (2), p.132-137

1998

Volltextzugriff (PDF)

Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

Nature genetics, 1995-09, Vol.11 (1), p.83-86

1995

Volltextzugriff (PDF)

1 – 25 von 2.406

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.109)
Mit Volltextzugriff
(2.057)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

4 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(1.514)
Life Sciences & Biomedicine
(1.079)
Humans
(803)
Male
(480)
Biological And Medical Sciences
(463)
Female
(434)
Medical Sciences
(357)
Animals
(343)
Physical Sciences
(324)
Adult
(254)
Middle Aged
(238)
Aged
(177)
Technology
(165)
Physics
(144)
Exact Sciences And Technology
(131)
Mice
(129)
Adolescent
(123)
Fundamental And Applied Biological Sciences. Psychology
(123)
Chemistry
(114)
Surgery
(101)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(12)

Menü

Weitere Dienste

Einstellungen

Long-term degradation of optical devices on the Moon

Laser ranging to the lost Lunokhod 1 reflector

Mutations in EXPH5 result in autosomal recessive inherited skin fragility

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Fifteen Years of Millimeter Accuracy Lunar Laser Ranging with APOLLO: Data Set Characterization

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Beta defensin-3 engineered epidermis shows highly protective effect for bacterial infection

APOLLO: millimeter lunar laser ranging

An absolute calibration system for millimeter-accuracy APOLLO measurements

Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma

Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family

Lunar eclipse observations reveal anomalous thermal performance of Apollo reflectors

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1

Gap junction development in the human fetal hair follicle and bulge region

The Apache Point Observatory Lunar Laser-ranging Operation (APOLLO) : Two Years of Millimeter-Precision Measurements of the Earth-Moon Range

Dangerousness, mental disorder, and responsibility

NICE, the draft fertility guideline and dodging the big question

Hemidesmosomes Show Abnormal Association with the Keratin Filament Network in Junctional Forms of Epidermolysis Bullosa

Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

Suchergebnisse filtern