Molecular genetic analysis of NIDDM. Status and prospects

Single-Nucleon Transfer on Unstable ^{59}Cu Probes the NiCu Cycle in Astrophysical X-Ray Bursts.

Physical review letters·2026

Beta-Decay Half-Lives beyond ^{54}Ca: A Systematic Survey of Decay Properties Approaching the Neutron Dripline.

Physical review letters·2026

Constraining the Synthesis of the Lightest p Nucleus ^{74}Se.

Physical review letters·2025

Crust Composition and the Shallow Heat Source in KS 1731-260.

Physical review letters·2025

Precision Mass Measurements around ^{84}Mo Rule Out ZrNb Cycle Formation in the Rapid Proton-Capture Process at Type I X-Ray Bursts.

Physical review letters·2025

Universal Effective Charges in the sd and fp Shells.

Physical review letters·2025

Autoantibodies to glutamate decarboxylase detected in diabetes-prone BB/OK rats do not distinguish onset of diabetes.

Experimental and clinical endocrinology·1994

Urinary excretion of hydroxy-pyridinium cross-links of collagen reflects skeletal growth velocity in normal children.

Experimental and clinical endocrinology·1994

Tissue regenerates of adrenal cortex with a physiological function twelve years after bilateral total adrenalectomy for Cushing's syndrome.

Experimental and clinical endocrinology·1994

Thyroid hormone deiodination in target tissues--a regulatory role for the trace element selenium?

Experimental and clinical endocrinology·1994

Effects of music treatment on salivary cortisol in patients exposed to pre-surgical stress.

Experimental and clinical endocrinology·1994

Systolic ventricular function in acute hypothyroidism: a study using Doppler echocardiography.

Experimental and clinical endocrinology·1994

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

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Molecular genetic analysis of NIDDM. Status and prospects

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Single-Nucleon Transfer on Unstable ^{59}Cu Probes the NiCu Cycle in Astrophysical X-Ray Bursts.

Beta-Decay Half-Lives beyond ^{54}Ca: A Systematic Survey of Decay Properties Approaching the Neutron Dripline.

Constraining the Synthesis of the Lightest p Nucleus ^{74}Se.

Crust Composition and the Shallow Heat Source in KS 1731-260.

Precision Mass Measurements around ^{84}Mo Rule Out ZrNb Cycle Formation in the Rapid Proton-Capture Process at Type I X-Ray Bursts.

Universal Effective Charges in the sd and fp Shells.

Autoantibodies to glutamate decarboxylase detected in diabetes-prone BB/OK rats do not distinguish onset of diabetes.

Urinary excretion of hydroxy-pyridinium cross-links of collagen reflects skeletal growth velocity in normal children.

Tissue regenerates of adrenal cortex with a physiological function twelve years after bilateral total adrenalectomy for Cushing's syndrome.

Thyroid hormone deiodination in target tissues--a regulatory role for the trace element selenium?

Effects of music treatment on salivary cortisol in patients exposed to pre-surgical stress.

Systolic ventricular function in acute hypothyroidism: a study using Doppler echocardiography.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

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