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Keyword Connections
heterozygous
Journals
1
1
BMC pulmonary medicine
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Bibliographies
25
1
serotonin transporter genotype modulates the gut microbiota composition in young rats, an effect augmented by early life stress
2
pre-weaning performance evaluation of a multibreed aberdeen angus × nellore population using different genetic models avaliação do desempenho na pré desmama de uma população bovina multirracial aberdeen angus × nelore utilizando diferentes modelos genéticos
3
a simple pcr-rflp method for genetic phase determination in compound heterozygotes
4
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
5
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
6
A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2.
7
Use of ivacaftor in late diagnosed cystic fibrosis monozygotic twins heterozygous for F508del and R117H-7T - a case report.
8
A Substantial Proportion of Apparently Heterozygous TP53 Pathogenic Variants Detected with a Next-Generation Sequencing Hereditary Pan-Cancer Panel Are Acquired Somatically.
9
Frequency of heterozygous TET2 deletions in myeloproliferative neoplasms
10
The APoE∗3-Leiden heterozygous glucokinase knockout mouse as novel translational disease model for type 2 diabetes, dyslipidemia, and diabetic atherosclerosis
11
Heterozygous p53-R280T Mutation Enhances the Oncogenicity of NPC Cells Through Activating PI3K-Akt Signaling Pathway.
12
compound heterozygous mutations associated with autophagic impairment cause cerebral infarction in Pompe disease.
13
[Pathophysiological Study on Thoracic Ascending Aorta of Mice with 11 Heterozygous Mutation in Norepinephrine-induced Hypertension Model].
14
Molecular characterization of a genetic variant of the steroid hormone- binding globulin gene in heterozygous subjects
15
assessment of oxidative stress parameters of brain-derived neurotrophic factor heterozygous mice in acute stress model
16
a case of chronic myeloid leukemia in a patient of double heterozygous hb-e beta thalassemia
17
a novel heterozygous missense mutation in gnat1 leads to autosomal dominant riggs type of congenital stationary night blindness
18
neural activity changes underlying the working memory deficit in alpha-camkii heterozygous knockout mice
19
novel missense variant in heterozygous state in the brpf1 gene leading to intellectual developmental disorder with dysmorphic facies and ptosis
20
a rare association of giant adrenal myelolipoma in a young female double heterozygous for hbd punjab and β-thalassemia trait
21
establishment of mui009 – a human induced pluripotent stem cells from a 32 year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2
22
acute hepatitis in a child heterozygous for the i259v mefv gene variant
23
variations in the 3′utr of the cyp21a2 gene in heterozygous females with hyperandrogenaemia
24
autosomal recessive congenital sensorineural hearing loss due to a novel compound heterozygous ptprq mutation in a chinese family
25
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease
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