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660-690 / 1000+ results![Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation](/images/research/ca31179e-caff-48d2-867e-6442bc3b67a2/small/27748.jpg)
research Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.
![Association Between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss](/images/research/b1fae399-1818-41b9-9d8d-390d17aed549/small/15667.jpg)
research Association Between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
Men with a family history of hair loss on their mother's side are more likely to have female pattern hair loss.
![Clinical Course of the First Japanese Family with Marie Unna Hereditary Hypotrichosis: A Follow-Up Report](/images/research/0b931ebd-cd8d-4a59-a08e-03e896fb21cc/small/17932.jpg)
research Clinical Course of the First Japanese Family with Marie Unna Hereditary Hypotrichosis: A Follow-Up Report
The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.
research Gene Detection in a Family With Monilethrix and Observation of the Treatment Effect With 5% Topical Minoxidil
![The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases](/images/research/43f845a1-e361-471f-b8b3-1564c4a4abfe/small/14689.jpg)
research The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.
![Roles of Jumonji and Jumonji Family Genes in Chromatin Regulation and Development](/images/research/59f92c66-c23a-4e2c-bea5-5567d7e3090c/small/20000.jpg)
research Roles of Jumonji and Jumonji Family Genes in Chromatin Regulation and Development
Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.
![The Human Type I Keratin Gene Family: Characterization of New Hair Follicle Specific Members and Evaluation of the Chromosome 17q21.2 Gene Domain](/images/research/416b3037-7363-43be-900c-53131f990641/small/29546.jpg)
research The Human Type I Keratin Gene Family: Characterization of New Hair Follicle Specific Members and Evaluation of the Chromosome 17q21.2 Gene Domain
The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.
research A Small Multigene Hydroxyproline-O-Galactosyltransferase Family Functions in Arabinogalactan-Protein Glycosylation, Growth, and Development in Arabidopsis
Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.
research Keratosis Follicularis Spinulosa Decalvans: A Family Study of Seven Male Cases and Six Female Carriers
The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.
![Keratosis Follicularis Spinulosa Decalvans in a Family](/images/research/8d0a4ff6-002f-4feb-bd5c-c706a5a57bfa/small/27813.jpg)
research Keratosis Follicularis Spinulosa Decalvans in a Family
KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.
![Cloning of the Human Phenol Sulfotransferase Gene Family: Three Genes Implicated in the Metabolism of Catecholamines, Thyroid Hormones, and Drugs](/images/research/d35cd53c-31fb-4ea4-a908-f41e55a1b140/small/15558.jpg)
research Cloning of the Human Phenol Sulfotransferase Gene Family: Three Genes Implicated in the Metabolism of Catecholamines, Thyroid Hormones, and Drugs
Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.
research Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability Within a Pakistani Family
A specific gene mutation causes varying hair loss severity in a Pakistani family.
research Expanding Phenotype of Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis Caused by FAM111B Mutations: Report of an Additional Family Raising the Question of Cancer Predisposition and a Short Review of Early-Onset Poikiloderma
The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.
![Analysis of the FGF Gene Family Provides Insights into Aquatic Adaptation in Cetaceans](/images/research/ca29c64b-8901-4442-aa7a-4b9093228a3d/small/30882.jpg)
research Analysis of the FGF Gene Family Provides Insights into Aquatic Adaptation in Cetaceans
Whale genes show changes that help them live in water, like less hair and better flippers.
![FOXN1 Italian Founder Mutation in Indian Family: Implications in Prenatal Diagnosis](/images/research/0e26e81d-eb69-43e1-9acb-b9ebd65bfba5/small/35812.jpg)
research FOXN1 Italian Founder Mutation in Indian Family: Implications in Prenatal Diagnosis
A rare genetic mutation found in an Indian family can be detected through prenatal screening.
research Characterization of Human Keratin-Associated Protein 1 Family Members
Mutations in hKAP1 genes may cause hereditary hair disorders.
![Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth](/images/research/2b621db4-193e-4730-be04-4f6cb8ad86b9/small/29263.jpg)
research Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
Low ERCC3 gene activity is linked to non-pigmented hair growth.
![Natural Course of Epidermolysis Bullosa Simplex with Mottled Pigmentation in a Japanese Family with the p.P25L Mutation in KRT5](/images/research/0251c6e7-6899-42a5-b776-bc66c1537f30/small/13467.jpg)
research Natural Course of Epidermolysis Bullosa Simplex with Mottled Pigmentation in a Japanese Family with the p.P25L Mutation in KRT5
The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.
research Atrichia With Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
New genetic mutations causing hair loss were found in a Chinese family.
research A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.
research Spatiotemporal Expression Characterization of KRTAP6 Family Genes and Its Effect on Wool Traits
KRTAP6 genes affect wool quality in sheep.
![Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family](/images/research/51e4692a-d98a-4e56-9504-5de180875b37/small/32989.jpg)
research Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.
![Validity and Reliability of the Thai Version of the Family Dermatology Life Quality Index](/images/research/45997f2d-6a42-4a02-82d8-84a7172561fd/small/20630.jpg)
research Validity and Reliability of the Thai Version of the Family Dermatology Life Quality Index
The Thai version of the Family Dermatology Life Quality Index is a reliable and valid tool for assessing the quality of life of patients' families.
![WNT10B (Wingless-Type MMTV Integration Site Family): Role in Biological Processes and Diseases](/images/research/b3743705-9dd2-4307-8085-1d185e657a5d/small/19401.jpg)
research WNT10B (Wingless-Type MMTV Integration Site Family): Role in Biological Processes and Diseases
WNT10B is linked to cancer development and affects survival and disease progression in various cancers.
research Androgenetic Alopecia: A Case Report and Family Survey
research The Roles of Hepatocyte Growth Factor Family Members in Androgen-Regulation of Human Hair Growth: A Comparison of the Expression of Hepatocyte Growth Factor Family Members, HGF and MSP, and Their Receptors, c-Met and RON, in Isolated Hair Follicles from Normal and Androgenetic Alopecia (Balding) Scalp
![Identification of a Novel PNPLA1 Mutation in a Spanish Family with Autosomal Recessive Congenital Ichthyosis](/images/research/8a126362-88a3-40a4-bc17-8e9dc3d451ab/small/16180.jpg)
research Identification of a Novel PNPLA1 Mutation in a Spanish Family with Autosomal Recessive Congenital Ichthyosis
A new gene mutation linked to a skin condition was found in a Spanish family.
![Marie Unna Hereditary Hypotrichosis: Identification of a U2HR Mutation in the Family from the Original 1925 Report](/images/research/a42dc848-8882-427f-8f31-30c1586d8d86/small/26181.jpg)
research Marie Unna Hereditary Hypotrichosis: Identification of a U2HR Mutation in the Family from the Original 1925 Report
Researchers found a gene mutation responsible for a rare hair loss condition.
![Novel Missense Mutation in the EDA Gene in a Family Affected by Oligodontia](/images/research/dba79303-e79a-4eb9-9f41-82db4b92951d/small/18557.jpg)
research Novel Missense Mutation in the EDA Gene in a Family Affected by Oligodontia
Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.