UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 608

Sortiert nach

Field test of quantum key distribution in the Tokyo QKD Network

Optics express, 2011-05, Vol.19 (11), p.10387-10409

2011

Volltextzugriff (PDF)

Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients

Clinical genetics, 2013-02, Vol.83 (2), p.135-144

2013

Volltextzugriff (PDF)

Cracking of n-butane over alkaline earth-containing HZSM-5 catalysts

Catalysis letters, 2002-12, Vol.84 (3-4), p.259-264

2002

Volltextzugriff (PDF)

Substituted effects of superconducting and magnetic states in reentrant superconductor Tm5Rh6Sn18

Physica. C, Superconductivity, 2010-12, Vol.470 (SUP1), p.S539-S540

2010

Volltextzugriff (PDF)

Engineering of optical continuous-variable qubits via displaced photon subtraction: multimode analysis

Journal of modern optics, 2011-02, Vol.58 (3-4), p.266-275

2011

Volltextzugriff (PDF)

Enhanced head-twitch response to 5-HT-related agonists in thiamine-deficient mice

Journal of Neural Transmission, 2007-08, Vol.114 (8), p.1003-1010

2007

Volltextzugriff (PDF)

Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes

Human molecular genetics, 2003-08, Vol.12 (15), p.1823-1837

2003

Volltextzugriff (PDF)

Dehydrogenative cracking of n-butane over modified HZSM-5 catalysts

Catalysis letters, 2002-07, Vol.81 (1-2), p.83-88

2002

Volltextzugriff (PDF)

Experimental creation of a fully inseparable tripartite continuous-variable state

Physical review letters, 2003-08, Vol.91 (8), p.080404-080404, Article 080404

2003

Volltextzugriff (PDF)

Dehydrogenative cracking of n-butane using double-stage reaction

Applied catalysis. A, General, 2002-04, Vol.230 (1), p.195-202

2002

Volltextzugriff (PDF)

Clinical and molecular analyses on two Japanese families with spinocerebellar ataxia type 23

Journal of the neurological sciences, 2017-10, Vol.381, p.307-307

2017

Volltextzugriff (PDF)

The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females

Cytogenetic and Genome Research, 2002, Vol.99 (1-4), p.276-284

2002

Volltextzugriff (PDF)

Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements

American journal of human genetics, 2003-05, Vol.72 (5), p.1101-1116

2003

Volltextzugriff (PDF)

A stable acentric marker chromosome : possible existence of an intercalary ancient centromere at distal 8p

American journal of human genetics, 1994-12, Vol.55 (6), p.1202-1208

1994

Volltextzugriff (PDF)

Sotos syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats

Human molecular genetics, 2005-02, Vol.14 (4), p.535-542

2005

Volltextzugriff (PDF)

Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression

Journal of human genetics, 2002-01, Vol.47 (10), p.511-516

2002

Volltextzugriff (PDF)

Cyclodehydration of diethylene glycol (DEG) catalyzed by clay mineral sepiolite

Journal of molecular catalysis. A, Chemical, 1999-06, Vol.142 (2), p.237-245

1999

Volltextzugriff (PDF)

Scanning electron microscopy of desiccation-tolerant and -sensitive microspore-derived embryos of Brassica napus L

Plant cell reports, 1999-03, Vol.18 (7/8), p.595-600

1999

Volltextzugriff (PDF)

'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation

Clinical genetics, 2003-01, Vol.63 (1), p.79-81

2003

Volltextzugriff (PDF)

Paroxysmal Kinesigenic Choreoathetosis Locus Maps to Chromosome 16p11.2-q12.1

American journal of human genetics, 1999-12, Vol.65 (6), p.1688-1697

1999

Volltextzugriff (PDF)

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation

Molecular genetics and metabolism, 2005-09, Vol.86 (1), p.257-268

2005

Volltextzugriff (PDF)

Male sterility in alloplasmic Brassica rapa L. carrying Eruca sativa cytoplasm

Plant breeding, 1999-03, Vol.118 (1), p.82-84

1999

Volltextzugriff (PDF)

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR

Human genetics, 1999-01, Vol.104 (1), p.49-55

1999

Volltextzugriff (PDF)

Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements

Human genetics, 2004, Vol.114 (2), p.198-206

2004

Volltextzugriff (PDF)

1 – 25 von 608

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(478)
Mit Volltextzugriff
(449)

Publikationsform

Sprache

Englisch
(498)
Japanisch
(237)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(309)
Humans
(268)
Life Sciences & Biomedicine
(236)
Male
(195)
Female
(162)
Biological And Medical Sciences
(149)
Medical Sciences
(120)
Middle Aged
(115)
Adult
(100)
Aged
(93)
Animals
(87)
Physical Sciences
(65)
Physics
(48)
Genetics & Heredity
(43)
Technology
(41)
Rats
(38)
Exact Sciences And Technology
(37)
Fundamental And Applied Biological Sciences. Psychology
(36)
Urology & Nephrology
(35)
Nephrology. Urinary Tract Diseases
(32)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Field test of quantum key distribution in the Tokyo QKD Network

Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients

Cracking of n-butane over alkaline earth-containing HZSM-5 catalysts

Substituted effects of superconducting and magnetic states in reentrant superconductor Tm5Rh6Sn18

Engineering of optical continuous-variable qubits via displaced photon subtraction: multimode analysis

Enhanced head-twitch response to 5-HT-related agonists in thiamine-deficient mice

Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes

Dehydrogenative cracking of n-butane over modified HZSM-5 catalysts

Experimental creation of a fully inseparable tripartite continuous-variable state

Dehydrogenative cracking of n-butane using double-stage reaction

Clinical and molecular analyses on two Japanese families with spinocerebellar ataxia type 23

The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females

Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements

A stable acentric marker chromosome : possible existence of an intercalary ancient centromere at distal 8p

Sotos syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats

Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression

Cyclodehydration of diethylene glycol (DEG) catalyzed by clay mineral sepiolite

Measurement of 3He analyzing power for p-3He scattering using the polarized 3He target

Scanning electron microscopy of desiccation-tolerant and -sensitive microspore-derived embryos of Brassica napus L

'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation

Paroxysmal Kinesigenic Choreoathetosis Locus Maps to Chromosome 16p11.2-q12.1

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation

Male sterility in alloplasmic Brassica rapa L. carrying Eruca sativa cytoplasm

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR

Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements

Suchergebnisse filtern