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The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

research The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

7 citations , January 2015 in “Case reports in genetics”

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

research Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome

11 citations , January 2021 in “British Journal of Dermatology”

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

research Rational Design and Functionalization of Melt Electrowritten 4D Scaffolds for Biomedical Applications

January 2026 in “Nano-Micro Letters”

4D scaffolds made with melt electrowriting can change shape for use in medicine.

research Thirty Years of Autologous Platelet Concentrates: From Platelet‐Rich Plasma to Platelet‐Rich Fibrin

11 citations , August 2025 in “Journal of Periodontal Research”

Platelet-rich fibrin (PRF) is better for natural healing, especially in dental and medical treatments.

research Protein-based functional hydrogel improves cutaneous nerve repair and diabetic wound healing

9 citations , December 2024 in “Nano Research”

A protein-based hydrogel helps heal diabetic wounds and repair nerves.

research Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix

8 citations , July 2015 in “International Journal of Dermatology”

A new DSG4 gene mutation causes hair defects in a young girl.

research Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes

53 citations , June 2005 in “The journal of investigative dermatology/Journal of investigative dermatology”

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

research LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development

August 2019 in “Journal of Investigative Dermatology”

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

research Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz^ica) mice points to fuzzy as a key element of hair cycle control

20 citations , July 2005 in “Experimental dermatology”

The fuzzy gene is crucial for controlling hair growth cycles.

research Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality

1 citations , October 2023 in “BMC Genomics”

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

research Scalp and Calvarial Reconstruction

April 2021 in “Elsevier eBooks”

The document's conclusion cannot be provided because the document is not accessible or understandable.

research International Journal of Aesthetic and Restorative Surgery

May 1996 in “Hair transplant forum international”

I'm sorry, but I can't provide a summary without the content of the document.

research Issue Information

November 2019 in “Australasian Journal of Dermatology”

I cannot provide a conclusion without the content of the document.

research A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism

September 2025 in “Frontiers in Genetics”

The method effectively extracts high-quality DNA from marmoset hair, avoiding blood chimerism.

research Book Review

July 2006 in “Hair transplant forum international”

The document's conclusion cannot be determined as the content is not available for analysis.

research Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis

47 citations , September 2012 in “Human molecular genetics online/Human molecular genetics”

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

research PLATELET RİCH PLASMA RESULTS IN THE TREATMENT OF FEMUR HEAD AVASCULAR NECROSIS

July 2024 in “Bozok Tıp Dergisi”

Platelet-rich plasma treatment shows early improvement in femur head avascular necrosis.

research Volume Contents

December 2025 in “The Journal of Dermatology”

research Volume Contents

December 2024 in “The Journal of Dermatology”

research Dual-continuous microneedle patch integrating transdermal delivery of pH-sensitive licorzinc MOFs and Zn2+ hydrogel sensors for treating alopecia areata

22 citations , September 2024 in “Chemical Engineering Journal”

A new microneedle patch effectively and safely treats alopecia areata.

research “Finasteride”

June 2018 in “International Review of Intellectual Property and Competition Law”

research Deletion analysis of AGD1 reveals domains crucial for its plasma membrane recruitment and function in root hair polarity

11 citations , June 2017 in “Journal of cell science”

AGD1's PH domain is essential for its role in root hair growth and polarity.

research CHRONIC TELOGEN EFFLUVIUM – A SHORT REVIEW -

January 2015 in “International journal of current research and review”

The document's conclusion cannot be provided because the content is not accessible.

research WISP-1 induced by mechanical stress contributes to the fibrosis and hypertrophy of ligamentum flavum via the Hedgehog-Gli1 signaling

November 2020

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

research A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2

January 2023 in “Revista Paulista de Pediatria”

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

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Search:

Research

research The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

research Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome

research Rational Design and Functionalization of Melt Electrowritten 4D Scaffolds for Biomedical Applications

research Thirty Years of Autologous Platelet Concentrates: From Platelet‐Rich Plasma to Platelet‐Rich Fibrin

research Protein-based functional hydrogel improves cutaneous nerve repair and diabetic wound healing

research Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix

research Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes

research LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development

research Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz^ica) mice points to fuzzy as a key element of hair cycle control

research Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality

research Scalp and Calvarial Reconstruction

research International Journal of Aesthetic and Restorative Surgery

research Issue Information

research A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism

research Book Review

research Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis

research PLATELET RİCH PLASMA RESULTS IN THE TREATMENT OF FEMUR HEAD AVASCULAR NECROSIS

research Volume Contents

research Volume Contents

research Dual-continuous microneedle patch integrating transdermal delivery of pH-sensitive licorzinc MOFs and Zn2+ hydrogel sensors for treating alopecia areata

research “Finasteride”

research Deletion analysis of AGD1 reveals domains crucial for its plasma membrane recruitment and function in root hair polarity

research CHRONIC TELOGEN EFFLUVIUM – A SHORT REVIEW -

research WISP-1 induced by mechanical stress contributes to the fibrosis and hypertrophy of ligamentum flavum via the Hedgehog-Gli1 signaling

research A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2

research Voltammetric sensing of minoxidil using a molecularly imprinted polymer (MIP)-modified carbon paste electrode

research TRASER: Acute phase vascular and follicular changes

research The Third Annual ASHRS Conference – Rancho Mirage, California

research Wavelength-encoded laser particles for massively-multiplexed cell tagging

research 664 Understanding the pathogenesis of seborrhea-like dermatitis in the Mpzl3 knockout mice