research A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
A mutation in the VDR gene affects hair cycling without needing ligand binding.
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research ISHRS: Expanding FUE Education
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research Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.
research 원저 : 여성형 탈모에서 AP-FHG0604T의 유효성 및 안전성 평가에 관한 임상 연구
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research Megatransplants in Transition: A Pictorial Review
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research Cloning, computational analysis and expression profiling of steroid 5 alpha-reductase 1 (SRD5A1) gene during reproductive phases and ovatide stimulation in endangered catfish, Clarias magur
The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.
research 10.1063/5.0132123.1
research Subject Index, Vol. 7,1994
research A numerical study of aircraft empennage buffet
research Localization and Regulation of Expression of the FAR-17A Gene in the Hamster Flank Organs
research Notes from the Editor Emeritus, 2005–2007
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research Get the essential small equipment you need fast!
Buy the basic tools you need quickly.
research Cyberspace Chat
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research Message from the 2017 Surgical Assistants Chair
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research ABHRS President’s Corner
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research ABHRS President’s Corner
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research ABHRS President’s Corner
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research Subject Index Vol. 210, 2005
research Disposable Linear Slot Punches
research Issue Information
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research Editor's notes
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research 胃切除・腸切除術後の退院指導-パンフレットを使用して-
Certain amino acids in 5AR1 and 5AR2 are crucial for binding and resistance to Finasteride.
research Notes from the Editor Emeritus, 2002–04
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research Autumn 2021
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research Co-editor’s note
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research 842Combination therapy with rofecoxib and finasteride in the treatment of men with lower urinary tract symptoms (LUTS)
research STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.
research Review of the Literature
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research Review of the Literature
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research ABHRS holds exam in Capri, Italy
The ABHRS held a test in Capri, Italy.