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Research 751–780 of 1000+
- <i>ZmSPL10</i>, <i>ZmSPL14</i> and <i>ZmSPL26</i> act together to promote stigmatic papilla formation in maize through regulating auxin signaling and <i>ZmWOX3A</i> expression
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Thiopurine-induced Myelosuppression with Severe Sepsis in a Patient with Crohn's Disease: A Case Report
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Clinical and Laboratory Characteristics of Individuals Aged ≤17 Years With Homeostatic Iron Regulator (HFE) p.C282Y Homozygosity, a Common Hemochromatosis Genotype
- Uncombable hair in a case of Zellweger syndrome – A new association
- 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- The Effect of Platelet Rich Plasma on Wound Healing in the Repair of Experimental Penile Fractures
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- IL-17 axis is a significant driver of skin inflammation in Card14 mutant pityriasis rubra pilaris model mice
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Persistent Hypoglycemia and Macrosomia in a Newborn
- SAT-288 Successful Virilization of a PAIS Patient with a Missense Mutation In The Ligand-binding Domain Of The Androgen Receptor with Combined High-dose Testosterone and Aromatase Inhibitor
- <i>Hoxc13</i> mutant mice lack external hair
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse