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「"New MI "[Author]」の検索結果

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Mechanism of glucocerebrosidase activation and dysfunction in Gaucher disease unraveled by molecular dynamics and deep learning.

Introduction: Contemporary perspectives on congenital adrenal hyperplasia: impacts on reproduction.

Fertility in patients with nonclassical congenital adrenal hyperplasia.

FSIP1 regulates autophagy in breast cancer.

A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita.

FSH, Bone Mass, Body Fat, and Biological Aging.

Human hydroxymethylbilane synthase: Molecular dynamics of the pyrrole chain elongation identifies step-specific residues that cause AIP.

Actions of pituitary hormones beyond traditional targets.

Epitope-specific monoclonal antibodies to FSHβ increase bone mass.

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

FSIP1 binds HER2 directly to regulate breast cancer growth and invasiveness.

Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype.

Blocking FSH induces thermogenic adipose tissue and reduces body fat.

Stigma Associated with Classical Congenital Adrenal Hyperplasia in Women's Sexual Lives.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases.

Syndrome-Related Stigma in the General Social Environment as Reported by Women with Classical Congenital Adrenal Hyperplasia.

A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.

Steroid 21-Hydroxylase Deficiency in Congenital Adrenal Hyperplasia.

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