"Genetics and disease" trang 1 - tải miễn phí từ tailieuXANH
Ebook Braunwald's heart disease - Review and assessment (10th edition): Part 1

Ebook Braunwald's heart disease - Review and assessment (10th edition): Part 1
150    72    2
Recent developments in molecular genetics of plant disease resistance

Recent developments in molecular genetics of plant disease resistance
8    59    0
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder
16    2    1
Ebook Thompson & Thompson genetics in medicine (8th edition): Part 1

Ebook Thompson & Thompson genetics in medicine (8th edition): Part 1
217    139    4
Establishing the UK DNA Bank for motor neuron disease (MND)

Establishing the UK DNA Bank for motor neuron disease (MND)
8    2    1
First draft genome of Thecaphora frezii, causal agent of peanut smut disease

First draft genome of Thecaphora frezii, causal agent of peanut smut disease
4    2    1
Clinical Genetics in Nursing Practice Third Edition

Clinical Genetics in Nursing Practice Third Edition
1    50    0
Ebook Medical genetics at a glance (3rd edition): Part 2

Ebook Medical genetics at a glance (3rd edition): Part 2
126    78    0
Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population

Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population
10    2    1
The association of CD40 polymorphisms with CD40 serum levels and risk of systemic lupus erythematosus

The association of CD40 polymorphisms with CD40 serum levels and risk of systemic lupus erythematosus
6    3    1
BEYOND THE DISEASE MODEL OF MENTAL DISORDERS

BEYOND THE DISEASE MODEL OF MENTAL DISORDERS
244    38    0
Báo cáo khoa học: TEC family kinases in health and disease – loss-of-function of BTK and ITK and the gain-of-function fusions ITK–SYK and BTK–SYK

Báo cáo khoa học: TEC family kinases in health and disease – loss-of-function of BTK and ITK and the gain-of-function fusions ITK–SYK and BTK–SYK
10    38    0
Genetic polymorphisms of transcription factor NRF2 and of its host gene sulfiredoxin (SRXN1) are associated with cerebrovascular disease in a finnish cohort, the TAMRISK study

Genetic polymorphisms of transcription factor NRF2 and of its host gene sulfiredoxin (SRXN1) are associated with cerebrovascular disease in a finnish cohort, the TAMRISK study
5    57    0
Variation around the dominant viral genome sequence contributes to viral load and outcome in patients with Ebola virus disease

Variation around the dominant viral genome sequence contributes to viral load and outcome in patients with Ebola virus disease
20    195    1
Ebook Integrated pest and disease management in greenhouse crops: Part 2

Ebook Integrated pest and disease management in greenhouse crops: Part 2
125    17    1
Autophagy-mediated expression clusters are involved in immunity regulation of coronary artery disease

Autophagy-mediated expression clusters are involved in immunity regulation of coronary artery disease
14    7    1
Genome-wide characterization of copy number variations in the host genome in genetic resistance to Marek’s disease using next generation sequencing

Genome-wide characterization of copy number variations in the host genome in genetic resistance to Marek’s disease using next generation sequencing
12    5    1
Determining immune components necessary for progression of pigment dispersing disease to glaucoma in DBA/2J mice

Determining immune components necessary for progression of pigment dispersing disease to glaucoma in DBA/2J mice
11    2    1
Multi-view singular value decomposition for disease subtyping and genetic associations

Multi-view singular value decomposition for disease subtyping and genetic associations
12    2    1
Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication

Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication
11    2    1
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