Search

for
Search:

Sort by

Research

990-1000 / 1000+ results

LncRNA-000133 from Secondary Hair Follicle of Cashmere Goat: Identification, Regulatory Network, and Its Effects on Inductive Property of Dermal Papilla Cells

research LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells

18 citations , January 2019 in “Animal Biotechnology”

A newly found RNA in Cashmere goats may play a role in hair growth and development.

research Rare Case of Cutis Vertex Gyrata

July 2025 in “Journal of Medical Science And clinical Research”

A 21-year-old male has a rare scalp condition with excessive skin folds.

research The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep

January 2002 in “Agritrop (Cirad)”

The hr gene is linked to hair loss in Valle del Belice sheep.

research Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing

1 citations , March 2022 in “bioRxiv (Cold Spring Harbor Laboratory)”

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

research LGR5 is a Marker of Poor Prognosis in Glioblastoma and is Required for Survival of Brain Cancer Stem‐Like Cells

82 citations , July 2012 in “Brain pathology”

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

research Variant PADI3 in Central Centrifugal Cicatricial Alopecia

95 citations , February 2019 in “The New England Journal of Medicine”

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

research Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells

January 2024

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

Rhombencephalosynapsis Presenting Antenatally with Ventriculomegaly/Hydrocephalus in a Likely Case of Gomez–López-Hernández Syndrome

research Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez–López-Hernández syndrome

18 citations , December 2006 in “Clinical dysmorphology”

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

New Frontiers in CRISPR/Cas9 Delivery Systems for Gene Editing

research New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing

June 2022 in “Authorea (Authorea)”

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

research Characterization of X-Linked SNP genotypic variation in globally distributed human populations

31 citations , January 2010 in “GenomeBiology.com (London. Print)”

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

← Previous page