Pages that link to "Q60021347"
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The following pages link to Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers (Q60021347):
Displaying 19 items.
- 3-Dimensional Imaging Modalities for Phenotyping Genetically Engineered Mice (Q26999618) (← links)
- Genetic, epigenetic, and environmental contributions to neural tube closure (Q27015138) (← links)
- Strain-specific modifier genes ofCecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes (Q28510741) (← links)
- Maternal diet modulates the risk for neural tube defects in a mouse model of diabetic pregnancy (Q34560952) (← links)
- Neural tube defects in mice exposed to tap water (Q34587686) (← links)
- Design and implementation of a custom built optical projection tomography system (Q34984458) (← links)
- Osteoblast menin regulates bone mass in vivo (Q35080199) (← links)
- Exploring the tumors of multiple endocrine neoplasia type 1 in mouse models for basic and preclinical studies (Q35082433) (← links)
- Animal models of pituitary neoplasia (Q36486988) (← links)
- A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype (Q36856421) (← links)
- Care for patients with multiple endocrine neoplasia type 1: the current evidence base (Q37808142) (← links)
- Two ways to use imaging: focusing directly on mechanism, or indirectly via behaviour? (Q37938221) (← links)
- Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. (Q42695925) (← links)
- Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma. (Q45907440) (← links)
- N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice. (Q52373139) (← links)
- Correlation of mutant menin stability with clinical expression of multiple endocrine neoplasia type 1 and its incomplete forms (Q53227787) (← links)
- MiR-15a/miR-16-1 expression inversely correlates with cyclin D1 levels in Men1 pituitary NETs (Q58559392) (← links)
- Abnormal expression of menin predicts the pathogenesis and poor prognosis of adult gliomas (Q92432288) (← links)
- COMPASS and SWI/SNF complexes in development and disease (Q99863988) (← links)