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...

Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation

Human mutation, 2020-12, Vol.41 (12), p.2028-2057

2020

Volltextzugriff (PDF)

Hurt, tired and queasy: Specific variants in the ATPase domain of the TRAP1 mitochondrial chaperone are associated with common, chronic "functional" symptomatology including pain, fatigue and gastrointestinal dysmotility

Mitochondrion, 2015-07, Vol.23, p.64-70

2015

Volltextzugriff (PDF)

764 Comparison of Topical Silver Sulfadiazine and Triple Antibiotic Ointment in a Porcine PT Burn Model

Journal of burn care & research, 2023-05, Vol.44 (Supplement_2), p.S167-S167

2023

Volltextzugriff (PDF)

Measurement of Four Uterine NK Cell Subtypes Using Multiplexed Fluorescent Immunohistochemical Staining in Women with Repeated Implantation Failure

Journal of visualized experiments, 2024-10 (212)

2024

Volltextzugriff (PDF)

Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a second case report

European journal of pediatrics, 2014-07, Vol.173 (7), p.967-969

2014

Volltextzugriff (PDF)

Copy number variation analysis by next-generation sequencing enhances molecular diagnostic yield of lysosomal diseases

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S148-S148

2018

Volltextzugriff (PDF)

Genetic testing for lysosomal disorders in a commercial laboratory: Use of pathognomonic criteria in variant interpretation

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S101-S102

2018

Volltextzugriff (PDF)

Molecular diagnostic findings of lysosomal diseases in children and adults suspected to have inborn errors of metabolism

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S64-S64

2018

Volltextzugriff (PDF)

Mutations in choline-O-acetyltransferase are associated with treatable cognitive decline, dysautonomia, and adverse medication responses — Time to CHAT with your patients?

Mitochondrion, 2013-11, Vol.13 (6), p.926-927

2013

Volltextzugriff (PDF)

Systemwide efforts to improve student achievement

2006

Volltextzugriff (PDF)

Spectroscopic Sensing Characteristics of Novel Osmium Carbonyl Complexes to DNA and Other Polyanions

American journal of analytical chemistry, 2021, Vol.12 (7), p.277-293

2021

Volltextzugriff (PDF)

Chronic pain, fatigue, GI dysmotility and the mitochondrial chaperone TRAP1

Mitochondrion, 2015-09, Vol.24, p.S24

2015

Volltextzugriff (PDF)

A high predisposition to depression and anxiety in mothers and other matrilineal relatives of children with presumed maternally inherited mitochondrial disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-08, Vol.137B (1), p.20-24

2005

Volltextzugriff (PDF)

Tc-99m MDP detection of diffuse metastatic involvement of the liver by salivary gland mucoepidermoid carcinoma

Clinical nuclear medicine, 1995-11, Vol.20 (11), p.1018-1019

1995

Volltextzugriff (PDF)

Increased Generation of CD8+ T Cell Clones in p53 Mutant Mice

The Journal of immunology (1950), 1999-04, Vol.162 (7), p.3957-3960

1999

Volltextzugriff (PDF)

活化的巨噬细胞介导的胰岛异种移植排异反应与细胞因子表达上调的关系

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007, Vol.32 (1), p.26-35

Abhilash P. Chandra Li Ou-yang Jeffrey K. W. Wong Hong Ha Stacey N. Waiters Anita T. Patel Wayne J. Hawthorne Shou-nan YI

2007

Volltextzugriff (PDF)

A high predisposition to depression and anxiety in mothers and other matrilineal relatives of children with presumed maternally inherited mitochondrial disorders

American journal of medical genetics, 2005, Vol.137B (1), p.20-24

2005

Volltextzugriff (PDF)

Reovirus genomic diversity confers plasticity for protease utility during adaptation to intracellular uncoating

Journal of virology, 2023-10, Vol.97 (10), p.e0082823-e0082823

2023

Volltextzugriff (PDF)

Computationally Optimized Broadly Reactive Hemagglutinin Elicits Hemagglutination Inhibition Antibodies against a Panel of H3N2 Influenza Virus Cocirculating Variants

Journal of virology, 2017-12, Vol.91 (24)

2017

Volltextzugriff (PDF)

The Depression Anxiety Stress Scales-21 (DASS-21): Further Examination of Dimensions, Scale Reliability, and Correlates

Journal of clinical psychology, 2012-12, Vol.68 (12), p.1322-1338

2012

Volltextzugriff (PDF)

SCN3A deficiency associated with increased seizure susceptibility

Neurobiology of disease, 2017-06, Vol.102, p.38-48

2017

Volltextzugriff (PDF)

Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians

American journal of human genetics, 2013-01, Vol.92 (1), p.41-51

2013

Volltextzugriff (PDF)

Divergent effects of brief contemplative practices in response to an acute stressor: A randomized controlled trial of brief breath awareness, loving-kindness, gratitude or an attention control practice

PloS one, 2018-12, Vol.13 (12), p.e0207765-e0207765

2018

Volltextzugriff (PDF)

Substitution of marijuana for opioids in a national survey of US adults

PloS one, 2019-10, Vol.14 (10), p.e0222577-e0222577

2019

Volltextzugriff (PDF)

Area-Selective Atomic Layer Deposition for Resistive Random-Access Memory Devices

ACS applied materials & interfaces, 2023-09, Vol.15 (36), p.43087-43093

2023

Volltextzugriff (PDF)

1 – 25 von 454

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(418)
Mit Volltextzugriff
(367)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(452)
Chinesisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(263)
Life Sciences & Biomedicine
(227)
Humans
(192)
Female
(112)
Male
(109)
Middle Aged
(55)
Adult
(47)
Animals
(44)
Aged
(42)
Adolescent
(35)
Biological And Medical Sciences
(35)
Genetics & Heredity
(30)
Medical Sciences
(29)
Medicine
(28)
Science & Technology - Other Topics
(28)
Mutation
(26)
Patients
(26)
Biochemistry & Molecular Biology
(25)
Mice
(24)
Multidisciplinary Sciences
(24)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(12)

Menü

Weitere Dienste

Einstellungen

Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation

Hurt, tired and queasy: Specific variants in the ATPase domain of the TRAP1 mitochondrial chaperone are associated with common, chronic "functional" symptomatology including pain, fatigue and gastrointestinal dysmotility

764 Comparison of Topical Silver Sulfadiazine and Triple Antibiotic Ointment in a Porcine PT Burn Model

Measurement of Four Uterine NK Cell Subtypes Using Multiplexed Fluorescent Immunohistochemical Staining in Women with Repeated Implantation Failure

Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a second case report

Copy number variation analysis by next-generation sequencing enhances molecular diagnostic yield of lysosomal diseases

Genetic testing for lysosomal disorders in a commercial laboratory: Use of pathognomonic criteria in variant interpretation

Molecular diagnostic findings of lysosomal diseases in children and adults suspected to have inborn errors of metabolism

Mutations in choline-O-acetyltransferase are associated with treatable cognitive decline, dysautonomia, and adverse medication responses — Time to CHAT with your patients?

Systemwide efforts to improve student achievement

Spectroscopic Sensing Characteristics of Novel Osmium Carbonyl Complexes to DNA and Other Polyanions

Chronic pain, fatigue, GI dysmotility and the mitochondrial chaperone TRAP1

A high predisposition to depression and anxiety in mothers and other matrilineal relatives of children with presumed maternally inherited mitochondrial disorders

Tc-99m MDP detection of diffuse metastatic involvement of the liver by salivary gland mucoepidermoid carcinoma

Increased Generation of CD8+ T Cell Clones in p53 Mutant Mice

活化的巨噬细胞介导的胰岛异种移植排异反应与细胞因子表达上调的关系

A high predisposition to depression and anxiety in mothers and other matrilineal relatives of children with presumed maternally inherited mitochondrial disorders

Reovirus genomic diversity confers plasticity for protease utility during adaptation to intracellular uncoating

Computationally Optimized Broadly Reactive Hemagglutinin Elicits Hemagglutination Inhibition Antibodies against a Panel of H3N2 Influenza Virus Cocirculating Variants

The Depression Anxiety Stress Scales-21 (DASS-21): Further Examination of Dimensions, Scale Reliability, and Correlates

SCN3A deficiency associated with increased seizure susceptibility

Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians

Divergent effects of brief contemplative practices in response to an acute stressor: A randomized controlled trial of brief breath awareness, loving-kindness, gratitude or an attention control practice

Substitution of marijuana for opioids in a national survey of US adults

Area-Selective Atomic Layer Deposition for Resistive Random-Access Memory Devices

Suchergebnisse filtern